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Select 'All' to list all the chemical categories. Each character links to a view of all chemical categories whose name begin by it. The asterisk (*) links to a view of all categories whose name start with a special character (e.g. '('). You can search the table for a specific string within that specific view.
NameChemOnt IDDescription
Chemical entitiesCHEMONTID:9999999Constitutionally or isotopically distinct atoms, molecules, ions, ion pairs, radicals, radical ions, complexes, conformers etc., identifiable as a separately distinguishable entity.
Organic compoundsCHEMONTID:0000000Compounds that contain at least one carbon atom, excluding isocyanide/cyanide and their non-hydrocarbyl derivatives, thiophosgene, carbon diselenide, carbon monosulfide, carbon disulfide, carbon subsulfide, carbon monoxide, carbon dioxide, Carbon suboxide, and dicarbon monoxide.
Inorganic compoundsCHEMONTID:0000001Compounds that do not contain a C atom. Exceptions are made for isocyanide/cyanide and their non-hydrocarbyl derivatives, thiophosgene, carbon diselenide, carbon monosulfide, carbon disulfide, carbon subsulfide, carbon monoxide, carbon trioxide, carbon suboxide, and dicarbon monoxide.
Organoheterocyclic compoundsCHEMONTID:0000002Compounds containing a ring with least one carbon atom and one non-carbon atom.
Organosulfur compoundsCHEMONTID:0000004Organic compounds containing a carbon-sulfur bond.
Lipids and lipid-like moleculesCHEMONTID:0000012Fatty acids and their derivatives, and substances related biosynthetically or functionally to these compounds.
AllenesCHEMONTID:0000016Compounds in which one carbon atom has double bonds with each of its two adjacent carbon centers. The definition includes both the hydrocarbon molecules and their derivatives obtained by substitution.
BenzenoidsCHEMONTID:0002448Aromatic compounds containing one or more benzene rings.
Phenylpropanoids and polyketidesCHEMONTID:0000261Organic compounds that are synthesized either from the amino acid phenylalanine (phenylpropanoids) or the decarboxylative condensation of malonyl-CoA (polyketides). Phenylpropanoids are aromatic compounds based on the phenylpropane skeleton. Polyketides usually consist of alternating carbonyl and methylene groups (beta-polyketones), biogenetically derived from repeated condensation of acetyl coenzyme A (via malonyl coenzyme A), and usually the compounds derived from them by further condensations.
Organic acids and derivativesCHEMONTID:0000264Compounds an organic acid or a derivative thereof.
Alkaloids and derivativesCHEMONTID:0000279Naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic properties. Also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus.
Organic saltsCHEMONTID:0003865Organic compounds consisting of an assembly of cations and anions.
Organohalogen compoundsCHEMONTID:0000267Organic compounds containing a bond between a carbon atom and a halogen atom (At, F, Cl, Br, I).
Organometallic compoundsCHEMONTID:0000462Organic compounds containing a bond between a carbon atom and metal atom.
Organic nitrogen compoundsCHEMONTID:0004707Organic compounds containing a nitrogen atom.
Nucleosides, nucleotides, and analoguesCHEMONTID:0000289Compounds containing a nucleobase linked to a ribose or deoxyribose sugar via a beta-glycosidic linkage. The ribose or deoxyribose moiety bears at least a phosphate group in case of nucleotides.
Organic oxygen compoundsCHEMONTID:0004603Organic compounds that contain one or more oxygen atoms.
Organophosphorus compoundsCHEMONTID:0000400Organic compounds containing the phosphorus atom.
Homogeneous metal compoundsCHEMONTID:0000422Inorganic compounds that contain only metal atoms.
Homogeneous non-metal compoundsCHEMONTID:0000423Inorganic compounds that contain only metal elements.
Mixed metal/non-metal compoundsCHEMONTID:0000424Compounds that contains both metal and non metal atoms.
Miscellaneous inorganic compoundsCHEMONTID:0001568Inorganic compounds of miscellaneous structure, which can be a mixture of chemical elements of different types.
Lignans, neolignans and related compoundsCHEMONTID:0001392Plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.
Organic PolymersCHEMONTID:0003297Organic compounds, generally large molecules or macromolecules, which are composed of many repeating units.
Hydrocarbon derivativesCHEMONTID:0004150Derivatives of hydrocarbons obtained by substituting one or more carbon atoms by an heteroatom. They contain at least one carbon atom and heteroatom.
HydrocarbonsCHEMONTID:0002837Organic compounds made up only of carbon and hydrogen atoms.
Organic anionsCHEMONTID:0003608Organic compounds that have a negative electric charge.
Organic cationsCHEMONTID:0003609Organic compounds with a positive electric charge.
Organic zwitterionsCHEMONTID:0003610Organic neutral compounds having formal unit electrical charges of opposite sign.
CarbenesCHEMONTID:0003629The electrically neutral species H2C and its derivatives, in which the carbon is covalently bonded to two univalent groups of any kind or a divalent group and bears two non-bonding electrons, which may be spin-paired (singlet state) or spin-non-paired (triplet state). Subclasses of carbenes include acyl carbenes, imidoyl carbenes, and vinyl carbenes.
Organic 1,3-dipolar compoundsCHEMONTID:0003630Electrically neutral organic molecules carrying a positive and a negative charge in one of their major canonical descriptions. In most dipolar compounds the charges are delocalized; however the term is also applied to species where this is not the case. The term 1,3-dipolar compounds is used for those in which a significant canonical resonance form can be represented by a separation of charge over three atoms (in connection with 1,3-dipolar cycloadditions).
Inorganic saltsCHEMONTID:0003866Inorganic compounds consisting of an assembly of cations and anions.
CarbidesCHEMONTID:0004469Inorganic compounds containing a carbon atom combined with one or more elements of similar or lower electronegativity.
Organopnictogen compoundsCHEMONTID:0004557Compounds containing a bond between carbon a pnictogen atom. Pnictogens are p-block element atoms that are in the group 15 of the periodic table.
ThiepanesCHEMONTID:0000003Organic compounds containing a heptane ring in which one carbon atom is replaced by a sulfur atom.
BenzoxazolinesCHEMONTID:0000006Organic compounds containing a benzene ring fused to an oxazoline ring. Oxazoline is five-membered unsaturated ring with a nitrogen atom and an oxygen atom at the 1- and 3-position, respectively. Additionally, it contains two double bonds.
Organonitrogen compoundsCHEMONTID:0000278Organic compounds containing a nitrogen atom.
Thiocarbonyl compoundsCHEMONTID:0001198Organic compounds containing a functional group with the general structure R1C(=S)R2 (R1, R2=H, alkyl, aryl).
Organooxygen compoundsCHEMONTID:0000323Organic compounds containing a bond between a carbon atom and an oxygen atom.
Carboxylic acids and derivativesCHEMONTID:0000265Compounds containing a carboxylic acid group with the formula -C(=O)OH or a derivative thereof.
Benzene and substituted derivativesCHEMONTID:0002279Aromatic compounds containing one monocyclic ring system consisting of benzene.
BenzofuransCHEMONTID:0000301Organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.
AnthracenesCHEMONTID:0000018Organic compounds containing a system of three linearly fused benzene rings.
DibenzocycloheptenesCHEMONTID:0000019Compounds containing a dibenzocycloheptene moiety, which consists of two benzene rings connected by a cycloheptene ring.
FluorenesCHEMONTID:0000020Compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.
Indenes and isoindenesCHEMONTID:0000021Compounds containing an indene moiety(which consists of a cyclopentadiene fused to a benzene ring), or a isoindene moiety (which consists of a cyclopentadiene fused to cyclohexadiene ring).
NaphthacenesCHEMONTID:0000022Compounds containing a naphthacene moiety, which is a polyaromatic hydrocarbon made of four linearly fused benzene rings.
NaphthalenesCHEMONTID:0000023Compounds containing a naphthalene moiety, which consists of two fused benzene rings.
PentacenesCHEMONTID:0000024Compounds containing a pentacene moiety, which is consists of five linearly fused benzene rings.
Phenanthrenes and derivativesCHEMONTID:0000025Polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.
IndanesCHEMONTID:0000027Compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring.
CinnamaldehydesCHEMONTID:0000029Organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal.
Sulfamic acid derivativesCHEMONTID:0000039Organic compounds containing a sulfamic acid moiety or a derivative, with the general structure R1N(R2)S(=O)2OR3 (R1,R2,R3=H, alkyl, aryl).
Lignan lactonesCHEMONTID:0001510Lignans that contain a lactone moiety. They include 1-aryltetralin lactones, dibenzylbutyrolactone lignans, and podophyllotoxins, among others.
TetralinsCHEMONTID:0000048Polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.
LactonesCHEMONTID:0000050Cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.
Quinolines and derivativesCHEMONTID:0001253Compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.
Isoquinolines and derivativesCHEMONTID:0002566Aromatic polycyclic compounds containing an isoquinoline moiety, which consists of a benzene ring fused to a pyridine ring and forming benzo[c]pyridine.
BenzothiazepinesCHEMONTID:0000317Organic compounds containing a benzene fused to a thiazepine ring (a seven-membered ring with a nitrogen atom and a sulfur atom replacing two carbon atoms).
MorphinansCHEMONTID:0000058Polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.
Organic nitric acids and derivativesCHEMONTID:0000488Compounds containing an organonitric acid group or a derivative thereof.
MacrolactamsCHEMONTID:0000064Cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.
Metalloheterocyclic compoundsCHEMONTID:0002052Heterocyclic compounds contain one metal ring atom.
OxazepinesCHEMONTID:0000066Compounds containing an oxazepine moiety, which consists of an unsaturated aliphatic seven-member ring with one oxygen atom, a nitrogen atom, and five carbon atoms. Isomers of oxazepine include 1,2-oxazepine, 1,3-oxazepine,and 1,4-oxazepine.
DiazinesCHEMONTID:0001346Organic compounds containing a five-member heterocyclic compound with five nitrogen atoms, and two nitrogen atoms at positions 1 and 2 (Pyridazines), 1 and 3 (Pyrimidines), or 1 and 4 (Pyrazines).
ThiazepinesCHEMONTID:0000068Heterocyclic compounds containing a seven-member aromatic ring with five carbon atoms, one sulfur atom, and one nitrogen atom.
AzepinesCHEMONTID:0000069Organic compounds containing an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom.
OxetanesCHEMONTID:0000070Compounds containing an oxetane ring, which is a four-member saturated aliphatic ring with an oxygen, and three carbon atoms.
DiazepinesCHEMONTID:0000071Organic compounds containing a seven-member heterocyclic moiety with five nitrogen atoms, and two nitrogen atoms at positions 1 and 2 (1,2-Diazepines), 1 and 3 (1,3-Diazepines), or 1 and 4 (1,4-Diazepines).
BenzodiazepinesCHEMONTID:0000295Organic compounds containing a benzene ring fused to either isomers of diazepine(unsaturated seven-member heterocycle with two nitrogen atoms replacing two carbon atoms).
OxetenesCHEMONTID:0000073Compounds containing an oxetene ring, which is a four-member unsaturated aliphatic ring with an oxygen, three carbon atoms, and one CC double bond.
FuransCHEMONTID:0000076Compounds containing a furan ring, which is a five-member aromatic ring with one oxygen atom, four carbon atoms.
AzolesCHEMONTID:0000436Organic compounds comprising a five-member nitrogen heterocyclic ring containing at least one other non-carbon atom of either nitrogen, sulfur, or oxygen.
AzolinesCHEMONTID:0002490Azole derivatives obtained by conversion of one double bond of the azole ring to a single bond.
BenzopyrazolesCHEMONTID:0001629Organic compounds containing a benzene ring fused to a pyrazole ring. Pyrazole is a 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers.
OxazinesCHEMONTID:0000082Compounds containing an oxazine moiety, which consists of an unsaturated aliphatic six-member ring with one oxygen atom, a nitrogen atom, four carbon atoms, and two double bonds. Isomers of oxaphospholane include 1,2-oxazine, 1,3-oxazine, and 1,4-oxazine.
PyransCHEMONTID:0000086Compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds.
Pyridines and derivativesCHEMONTID:0000089Compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
PyrrolesCHEMONTID:0000090Compounds containing a pyrrole ring, which is a five-member aromatic heterocycle with one nitrogen atom and four carbon atoms.
PyrrolinesCHEMONTID:0000091Compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms.
TetrazinesCHEMONTID:0000092Organic compounds containing a tetrazine ring, which is a six-membered aromatic heterocycle made up of four nitrogen atoms and a two carbon atoms.
ThiazinesCHEMONTID:0000094Heterocyclic compounds containing an aliphatic unsaturated six-member ring with four carbon atoms, one sulfur atom, and one nitrogen. Isomers include 1,2-thiazines, 1,3-thiazines, and 1,4-thiazines.
ThiepinsCHEMONTID:0000096Heterocyclic compounds containing an unsaturated seven-member heterocycle, with six carbon atoms and one sulfur atom.
ThiophenesCHEMONTID:0000097Compounds containing a five-membered aromatic moiety made up of one sulfur atom and four carbon atoms.
TriazinesCHEMONTID:0000098Compounds containing a triazine ring, which is a heterocyclic ring, similar to the six-member benzene ring but with three carbons replaced by nitrogen atoms.
AzetidinesCHEMONTID:0000102Organic compounds containing a saturated four-member heterocycle where one nitrogen atom replaces a carbon atom.
AziridinesCHEMONTID:0000103Organic compounds containing a saturated three-member heterocycle with one amino group and two methylene groups.
AzirinesCHEMONTID:0000104Organic compounds containing an unsaturated three-member heterocycle with one amino group and a double bond.
DioxolanesCHEMONTID:0000105Compounds containing a dioxolane ring, which is a five-membered saturated ring of two oxygen atoms and three carbon atoms. The dioxolanes are divided in 1,2-dioxolanes, and 1,3-dioxolanes.
OxathiolanesCHEMONTID:0000106Compounds containing an oxathiolane moiety, which consists of a saturated aliphatic five-member ring with one oxygen atom, a sulfur atom, and three carbon atoms. Isomers of oxaphospholane include meta-oxathiolane, and ortho-oxathiolane.
OxazinanesCHEMONTID:0000107Compounds containing an oxazinane moiety, which consists of a saturated aliphatic six-member ring with one oxygen atom, a nitrogen atom, and four carbon atoms. Isomers of oxaphospholane include 1,2-oxazinane, 1,3-oxazinane, and 1,4-oxazinane.
AzolidinesCHEMONTID:0002491Azole derivatives obtained by conversion of both double bonds of the azole ring to single bonds, yielding a saturated ring.
Pteridines and derivativesCHEMONTID:0000109Polycyclic aromatic compounds containing a pteridine moiety, which consists of a pyrimidine fused to a pyrazine ring to form pyrimido(4,5-b)pyrazine.
BenzopyransCHEMONTID:0000123Organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.
Organic azidesCHEMONTID:0000126Compounds bearing the group N3, viz. -N=N+=N-; usually attached to carbon, e.g. PhN3 phenyl azide or azidobenzene.
Isoindoles and derivativesCHEMONTID:0001819Polycyclic compounds containing an isoindole moiety, which is structurally characterized by a cyclohexadiene fused to a pyrrole ring.
Azaspirodecane derivativesCHEMONTID:0000130Organic compounds containing a spirodecane moiety with at least one nitrogen atom.
PhenolsCHEMONTID:0000134Compounds containing a phenol moiety, which is a benzene bearing a hydroxyl group.
Phenol ethersCHEMONTID:0002341Aromatic compounds containing an ether group substituted with a benzene ring.
StilbenesCHEMONTID:0000253Organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.
Coumarins and derivativesCHEMONTID:0000145Polycyclic aromatic compounds containing a 1-benzopyran moiety with a ketone group at the C2 carbon atom (1-benzopyran-2-one).
Macrolides and analoguesCHEMONTID:0000147Organic compounds containing a lactone ring of at least twelve members.
BenzoxazepinesCHEMONTID:0000319Organic compounds containing a benzene fused to an oxazepine ring (a seven-membered ring with four carbon atoms, one oxygen atom, and a nitrogen atom).
PentacenequinonesCHEMONTID:0000154Compounds containing a pentacenequinone moiety, which consists of five linearly fused benzene ring, with at least one bearing two ketones.
EpoxidesCHEMONTID:0000159Compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).
LactamsCHEMONTID:0000160Compounds containing a lactam ring, which is a cyclic amide of amino carboxylic acids, having a 1-azacycloalkan-2-one structure (or an analogue having unsaturation or heteroatoms replacing one or more carbon atoms of the ring).
ThiolactamsCHEMONTID:0000166Cyclic thioamides, obtained by replacing the oxygen atom from a lactam ring with sulfur.
GlycerolipidsCHEMONTID:0000175Lipids formed by joining fatty acids to glycerol by ester bonds.
ImidazopyridinesCHEMONTID:0000328Organic polycyclic compounds containing an imidazole ring fused to a pyridine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.
TetracyclinesCHEMONTID:0000181Polyketides having an octahydrotetracene-2-carboxamide skeleton, substituted with many hydroxy and other groups.
Indoles and derivativesCHEMONTID:0000211Organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
DiazinanesCHEMONTID:0002389Organic compounds containing diazinane, a six-membered saturated heterocycle containing four carbon atoms and two nitrogen atoms.
Diazaspirononane derivativesCHEMONTID:0000191Organic heterocyclic compounds that contain a nine-membered saturated bicyclic moiety, consisting of two aliphatic saturated rings in a spiro-configuration, each of which contain a nitrogen atom. The bicyclic moiety is made up of two nitrogen and seven carbon atoms.
PyrrolopyrazinesCHEMONTID:0000343Compounds containing a pyrrolopyrazine moiety, which consists of a pyrrole ring fused to a pyrazine. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Pyrazine is a 6-membered ring consisting of six carbon atoms and two nitrogen centers at ring positions 1 and 4.
DioxolesCHEMONTID:0000193Compounds containing a dioxole ring, which is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. The dioxoles are divided in meta-dioxoles, and ortho-dioxoles.
PiperidinesCHEMONTID:0000195Compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.
Tetrapyrroles and derivativesCHEMONTID:0001455Polycyclic aromatic compounds containing four pyrrole rings joined by one-carbon units linking position 2 of one pyrrole ring to position 5 of the next.
PyrrolopyridinesCHEMONTID:0000213Compounds containing a pyrrolopyridine moiety, which consists of a pyrrole ring fused to a pyridine. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.
PyrrolidinesCHEMONTID:0000218Compounds containing a pyrrolidine ring, which is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
PyrrolizinesCHEMONTID:0000219Compounds containing a pyrrolizine moiety, which consists of a pyrrole ring fused to a pyrrolidine ring.
PyrrolizidinesCHEMONTID:0000220Compounds containing a pyrrolizidine, which is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.
QuinolizidinesCHEMONTID:0000221Compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.
QuinolizinesCHEMONTID:0000222Compounds containing a quinolizine moiety, which consists of two fused pyridine rings sharing a nitrogen atom.
ThiadiazinesCHEMONTID:0000224Cyclic organic compounds containing a thiadiazine ring, which is a six-member unsaturated heterocycle made up of one sulfur atom and two nitrogen atoms.
Organic oxoanionic compoundsCHEMONTID:0000463Organic compounds containing an oxoanion.
BenzothiepinsCHEMONTID:0000231Organic compounds containing a benzene fused to a thiepine ring (a seven-membered ring with six carbon atoms and one sulfur atom).
ThiolanesCHEMONTID:0000233Organic compounds containing thiolane, a five-member saturated ring containing four carbon atoms and a sulfur atom.
Ellagic acids and derivativesCHEMONTID:0000236Compounds containing an ellagic acid moiety (4,4',5,5',6,6'-Hexahydroxydiphenic acid 2,6,2',6'-dilactone) or a derivative thereof.
TanninsCHEMONTID:0000238Naturally occurring polyphenols which be categorized into four main classes: hydrolyzable tannin (based on ellagic acid or gallic acid), condensed tannins (made of oligomeric or polymeric proanthocyanidins), complex tannins (made of a catechin bound to a gallotannin or elagitannin), and phlorotannins (oligomers of phloroglucinol).
CamptothecinsCHEMONTID:0000240Heterocyclic compounds comprising a planar pentacyclic ring structure, that includes a pyrrolo[3,4-beta]-quinoline moiety (rings A, B and C), conjugated pyridone moiety (ring D) and one chiral center at position 20 within the alpha-hydroxy lactone ring with (S) configuration (the E-ring).
ThienoimidazolesCHEMONTID:0000243Heterocyclic compounds containing a thiophene ring fused to an imidazole ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Imidazole is 5-membered ring consisting of three carbon and two nitrogen centers at the 1- and 3-positions.
Biotin and derivativesCHEMONTID:0000244Organic compounds containing a ureido (tetrahydroimidizalone) ring fused with a tetrahydrothiophene ring.
ImidazopyrimidinesCHEMONTID:0001797Organic polycyclic compounds containing an imidazole ring fused to a pyrimidine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
IndolizidinesCHEMONTID:0000251Polycyclic compounds containing an indolizidine, which is a bicyclic heterocycle containing a saturated six-member ring fused to a saturated five-member ring, one of the bridging atoms being nitrogen.
QuinuclidinesCHEMONTID:0000252Compounds containing a 1-azabicyclo[2.2.2]octane moiety.
GlycerophospholipidsCHEMONTID:0000256Derivatives of glycerophosphoric acid that contains at least one O-acyl, or O-alkyl, or O-(1-alkenyl) group attached to the glycerol residue.
SphingolipidsCHEMONTID:0000257Lipids containing backbone of sphingoid bases (e.g. Sphinogsine, sphinganine) usually bound to a fatty acid derivative through N-acylation.
Steroids and steroid derivativesCHEMONTID:0000258Compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred.
Prenol lipidsCHEMONTID:0000259Lipids synthesized from the five-carbon-unit precursors isopentenyl diphosphate and dimethylallyl diphosphate.
Fatty AcylsCHEMONTID:0003909Organic molecules synthesized by chain elongation of an acetyl-CoA primer with malonyl-CoA (or methylmalonyl-CoA) groups that might contain a cyclic functionality and/or are substituted with heteroatoms.
Hydroxy acids and derivativesCHEMONTID:0000472Compounds comprising one or more hydroxy acid groups.
Organosulfenic acids and derivativesCHEMONTID:0000268Compounds derived from sulfenic acid, with the general formula R1SR2 ( R1= organyl, R2=any heteroatom).
Sulfinic acids and derivativesCHEMONTID:0000269Compounds derived from sulfinic acid, with the general formula RS(=O)R' ( R not H, R'=any heteroatom).
Organic sulfonic acids and derivativesCHEMONTID:0004434Compounds containing a sulfonic acid or derivative, with the general structure RS(=O)2X (R= H or organyl group, X=any heteroatom).
Organoalkaline-earth metal compoundsCHEMONTID:0000277Organic compounds containing an alkaline earth metal atom.
BenzazepinesCHEMONTID:0000293Organic compounds containing a benzene ring fused to an azepine ring (unsaturated seven-membered heterocycle with one nitrogen atom replacing a carbon atom).
BenzimidazolesCHEMONTID:0000294Organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds).
BenzodioxolesCHEMONTID:0000296Organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.
BenzoxazolesCHEMONTID:0000302Organic compounds containing a benzene fused to an oxazole ring Oxazole is five-membered aromatic ring with a nitrogen and an oxygen atoms at the 1- and 3-position, respectively.
PyrazolopyridinesCHEMONTID:0000304Compounds containing a pyrazolopyridine skeleton, which consists of a pyrazole fused to a pyridine. Pyrazole is 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers. Pyridine is a 6-membered ring with four carbon and one nitrogen atoms.
PyrazolopyrimidinesCHEMONTID:0000305Compounds containing a pyrazolopyrimidine skeleton, which consists of a pyrazole fused to a pyrimidine. Pyrazole is 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers. Pyrimidine is 6-membered ring consisting of four carbon atoms and two adjacent nitrogen atoms at the 1- and 3- ring position.
AzepanesCHEMONTID:0000307Organic compounds containing a saturated seven member heterocycle, with one nitrogen atom.
BenzothiazinesCHEMONTID:0000309Organic compounds containing a benzene fused to a thiazine ring (a six-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
BenzothiazolesCHEMONTID:0000311Organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
BenzothiophenesCHEMONTID:0000312Organic compounds containing a benzene fused to a thiepine ring (a five-membered ring with six carbon atoms and one sulfur atom).
TriazolopyrazinesCHEMONTID:0000313Compounds containing a triazole ring fused to a pyrazine ring. Triazole is a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Pyrazine is a 6-membered ring consisting of six carbon atoms and two nitrogen centers at ring positions 1 and 4.
TriazolopyridinesCHEMONTID:0000314Compounds containing a triazole ring fused to a pyridine ring. Triazole is a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.
BenzotriazolesCHEMONTID:0000315Organic compounds containing a benzene fused to a triazole ring (a five-membered ring with two carbon atoms and three nitrogen atoms).
PyrenesCHEMONTID:0001851Compounds containing a pyrene moiety, which consists four fused benzene rings, resulting in a flat aromatic system.
BetalainsCHEMONTID:0001435Organic compounds belonging to the class of Betaxanthins or Betacyanins. This class also contains derivatives of betalamic acid, which is the precursor of betalains.
Organic phosphonic acids and derivativesCHEMONTID:0000419Organic compounds containing phosphonic acid or a derivative thereof.
FlavonoidsCHEMONTID:0000334Plant secondary metabolites that contain the 2-phenylchromene skeleton. Plant secondary metabolites that contain the 2-phenylchromene skeleton.
ThienopyridinesCHEMONTID:0000344Heterocyclic compounds containing a thiophene ring fused to a pyridine ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.
Organometalloid compoundsCHEMONTID:0001370Organic compounds containing a metalloid atom.
IsoflavonoidsCHEMONTID:0002506Natural products derived from 3-phenylchromen-4-one.
ThietanesCHEMONTID:0000359Heterocyclic compounds containing a saturated four-member ring with three carbon atoms and one sulfur atom.
ThietesCHEMONTID:0000360Heterocyclic compounds containing an unsaturated aliphatic four-member ring with three carbon atoms, one sulfur atom, and one double bond.
Organic carbonic acids and derivativesCHEMONTID:0000364Compounds comprising the organic carbonic acid or a derivative thereof.
DioxanesCHEMONTID:0000368Compounds containing a dioxane ring, which is a six-membered saturated ring of two oxygen atoms and four carbon atoms. The dioxanes are divided in 1,2-dioxanes, 1,3-dioxanes, and 1,4-dioxanes.
ThiiranesCHEMONTID:0000377Heterocyclic compounds containing a saturated three-member ring with two carbon atoms and one sulfur atom.
DithietanesCHEMONTID:0000378Compounds comprising a dithietane moiety, which is four-member saturated ring containing two divalent sulfur atoms and two carbon atoms.
AporphinesCHEMONTID:0000381Quinoline alkaloids containing the dibenzo[de,g]quinoline ring system or a dehydrogenated derivative thereof.
Keto acids and derivativesCHEMONTID:0000389Organic compounds containing a ketone group and a carboxylic acid group.
Organic phosphines and derivativesCHEMONTID:0000401Organic compounds containing a phosphine derivative, with the general formula B1P(R2)R3 (R1-R3=alkyl, aryl).
Organic phosphoric acids and derivativesCHEMONTID:0000402Organic compounds containing phosphoric acid or a derivative thereof.
Organic sulfuric acids and derivativesCHEMONTID:0000403Organic compounds containing the sulfuric acid or a derivative thereof.
Organo-alkali-metal compoundsCHEMONTID:0001372Organic compounds containing an alkali metal atom.
Organotransition metal compoundsCHEMONTID:0001371Organic compounds containing a transition metal atom.
DioxetanesCHEMONTID:0000412Compounds containing a dioxetane ring, which is a four-member ring of two oxygen atoms and two carbon atoms. The dioxetanes are divided in 1,2-dioxetanes, and 1,3-dioxetanes.
Organic oxidesCHEMONTID:0003940Organic compounds containing an oxide group.
Boronic acid derivativesCHEMONTID:0000498Compounds comprising any derivative of the boronic acid functional group, with the general structure RB(X)Y (R=alkyl, aryl; X,Y= any O, N, Hal residue).
Homogeneous alkali metal compoundsCHEMONTID:0000425Inorganic compounds containing only metal atoms,with the largest atom being a alkali metal atom.
Homogeneous transition metal compoundsCHEMONTID:0000426Inorganic compounds containing only metal atoms,with the largest atom being a transition metal atom.
Homogeneous post-transition metal compoundsCHEMONTID:0000427Inorganic compounds containing only metal atoms,with the largest atom being a post-transition metal atom.
Homogeneous alkaline earth metal compoundsCHEMONTID:0000428Inorganic compounds containing only metal atoms,with the largest atom being a alkaline earth metal atom.
Homogeneous lanthanide compoundsCHEMONTID:0000429Inorganic compounds containing only metal atoms, with the largest atom being a lanthanide atom.
Homogeneous actinide compoundsCHEMONTID:0000430Inorganic compounds containing only metal atoms,with the largest atom being a transition metal atom.
Homogeneous metalloid compoundsCHEMONTID:0000431Inorganic compounds containing only metal atoms,with the largest atom being a metalloid atom.
Homogeneous halogensCHEMONTID:0000432Inorganic non-metallic compounds in which the largest atom is a nobel gas.
Homogeneous noble gasesCHEMONTID:0000433Inorganic non-metallic compounds in which the largest atom is a halogen atom.
Homogeneous other non-metal compoundsCHEMONTID:0000434Inorganic non-metallic compounds in which the largest atom belongs to the class of 'other nonmetals'.
Non-metal oxoanionic compoundsCHEMONTID:0000435Inorganic non-metallic compounds containing an oxoanion.
Other non-metal halidesCHEMONTID:0000437Inorganic compounds containing 'other non-metals' and halogen.
Alkali metal saltsCHEMONTID:0000438Inorganic salt compounds in which the heaviest ionic metal atom is an alkali metal.
Alkaline earth metal saltsCHEMONTID:0000439Inorganic halogenic compounds in which the heaviest metal atom is an alkaline earth metal.
Lanthanide saltsCHEMONTID:0000440Inorganic halogenic compounds in which the heaviest metal atom is a lanthanide.
Actinide saltsCHEMONTID:0000441Inorganic halogenic compounds in which the heaviest metal atom is an actinide.
Metalloid saltsCHEMONTID:0000442Inorganic halogenic compounds in which the heaviest metal atom is a metalloid.
Transition metal saltsCHEMONTID:0000443Inorganic halogenic compounds in which the heaviest metal atom is a transition metal.
Post-transition metal saltsCHEMONTID:0000444Inorganic halogenic compounds in which the heaviest metal atom is a post-transition metal.
Alkali metal oxoanionic compoundsCHEMONTID:0000445Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is an alkali metal.
Alkaline earth metal oxoanionic compoundsCHEMONTID:0000446Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Lanthanide oxoanionic compoundsCHEMONTID:0000447Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is a lanthanide.
Actinide oxoanionic compoundsCHEMONTID:0000448Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is an actinide.
Metalloid oxoanionic compoundsCHEMONTID:0000449Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is a metalloid.
Transition metal oxoanionic compoundsCHEMONTID:0000450Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is a transition metal.
Post-transition metal oxoanionic compoundsCHEMONTID:0000451Inorganic oxoanionic compounds in which the heaviest atom not in an oxoanion is a post-transition metal.
Other non-metal organidesCHEMONTID:0000453Inorganic compounds belonging to either of the other non-metal Hydrides, other non-metal nitrides, other non-metal oxides, or the other non-metal sulfides.
Halogen organidesCHEMONTID:0000454Inorganic compounds belonging to either the halogen hydrides, halogen nitrides, halogen oxides, or halogen sulfides.
Actinide organidesCHEMONTID:0000455Organic compounds belonging to either the actinide hydrides, actinide nitrides, actinide oxides, or actinide sulfides.
Alkali metal organidesCHEMONTID:0000456Inorganic compounds belonging either to the alkali metal hydrides, the alkali metal nitrides, the alkali metal oxides, or the alkali metal sulfides.
Alkaline earth metal organidesCHEMONTID:0000457Inorganic compounds belonging either to the alkaline earth metal hydrides, the alkaline earth metal nitrides, the alkaline earth metal oxides, or the alkaline earth metal sulfides.
Post-transition metal organidesCHEMONTID:0000458Inorganic compounds belonging either to the post-transition metal hydrides, post-transition metal nitrides, post-transition metal oxides, or the post-transition metal sulfides.
Lanthanide organidesCHEMONTID:0000459Inorganic compounds belonging to either the lanthanide hydrides, lanthanide nitrides, lanthanide oxides, lanthanide sulfides.
Metalloid organidesCHEMONTID:0000460Inorganic compounds belonging to either of the metalloid hydrides, metalloid nitrides, metalloid oxides, metalloid sulfides.
Transition metal organidesCHEMONTID:0000461Inorganic compounds belonging to either the alkaline earth metal hydrides, alkaline earth metal nitrides, alkaline earth metal oxides, alkaline earth metal sulfides.
AcetylenedicarboxylatesCHEMONTID:0000464Organic compounds containing but-2-ynedioic acid or a derivative thereof.
Cinnamic acids and derivativesCHEMONTID:0000476Organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.
Purine nucleosidesCHEMONTID:0000479Compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
Pyrimidine nucleosidesCHEMONTID:0000480Compounds comprising a pyrimidine base attached to a ribosyl or deoxyribosyl moiety.
TrithiolanesCHEMONTID:0000482Organic compounds containing a six-member aliphatic saturated heterocycle made up of three sulfur atoms and two carbon atoms.
DithiolanesCHEMONTID:0000484Compounds containing a dithiolane ring, which consists of a sulfur heterocycle derived from cyclopentane by replacing two CH2 groups with thioether groups.
SulfoxidesCHEMONTID:0000491Compounds containing a sulfoxide functional group, with the structure RS(=O)R' (R,R' not H).
Tropane alkaloidsCHEMONTID:0000492Organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]octane.
ThiaziridinesCHEMONTID:0000493Organic heterocyclic compounds with a 3-membered saturated ring with a thioether group and an amine group in the 1 and 2 positions, respectively.
Carboximidic acids and derivativesCHEMONTID:0002285Compounds containing a carboximidic group, with the general formula R-C(=NR1)OR2.
SulfonylsCHEMONTID:0001157Compounds containing the sulfonyl group, with the general structure RS(=O)2R' ( R,R' must not be H).
Sulfonyl halidesCHEMONTID:0000506Compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to a halogen atom.
Organic sulfonium compoundsCHEMONTID:0000508Organic compounds containing the sulfonium cation, with the general formula [SR3]+ (R=any atom).
SultamsCHEMONTID:0000509Sulfonamides in which the S-N bond is part of a ring.
ThioamidesCHEMONTID:0000510Organic compounds containing the functional group with the general structure R-CS-NR'R, where R, R', and R are organic groups.
Benzimidazole ribonucleosides and ribonucleotidesCHEMONTID:0000663Nucleosides with a structure that consists of an imidazole moiety of benzimidazole is N-linked to a ribose (or deoxyribose). Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
ImidazothiazolesCHEMONTID:0000756Organic polycyclic compounds containing an imidazole ring fused to a thiazole ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Thiazole is a 6-membered ring that contains both sulfur and nitrogen.
OxaphospholanesCHEMONTID:0000782Compounds containing an oxaphospholane moiety, which consists of a saturated aliphatic five-member ring with two oxygen atoms, a phosphorus atom, and two carbon atoms. Isomers of oxaphospholane include 1,2-oxaphosphane, and 1,3-oxaphospholane.
ImidazodithiazolesCHEMONTID:0000796Organic compounds containing an imidazole ring fused to a dithiazole ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Dithiazole is a five-membered heterocycle containing two sulfur atoms, one nitrogen atom, three carbon atoms and two double bonds
DioxaphospholanesCHEMONTID:0000822Cyclic organic compounds containing a five-member aliphatic single-bonded ring, with a phosphorine atom and two oxygen atoms at the ring positions 1, 2, and 3 respectively.
DibenzazecinsCHEMONTID:0001008Polycyclic aromatic compounds containing two benzene rings joined by an azecin ring.
Glycinamide ribonucleotidesCHEMONTID:0001014Compounds in which the amide N atom of glycineamide is linked to the C-1 of a ribosyl (or deoxyribosyl) moiety. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Saturated hydrocarbonsCHEMONTID:0004474Hydrocarbons that contains only saturated carbon atoms, which are linked to one another through single bonds. These includes alkanes and cycloalkanes.
Acyl halidesCHEMONTID:0002865Organic compounds with the general structure RC(=O)X, where X is a halogen atom.
Alkyl halidesCHEMONTID:0002867Organic compounds containing a linear aliphatic chain (or ring system) carrying a C-X bond, where X is a halogen atom.
Aryl halidesCHEMONTID:0002866Organic compounds containing an aromatic ring (or ring system) carrying a C-X bond.
Imidoyl halidesCHEMONTID:0002870Organic compounds containing the imidoyl halide functional group, with the general structure R(X)C=NR' (R, R'=H, alkyl, aryl; X = halogen).
Organic sulfuryl halidesCHEMONTID:0002869Organic compounds containing the sulfuryl halide group.
Other mixed metal/non-metal oxoanionic compoundsCHEMONTID:0001442Inorganic compounds containing a non-metal atom linked to a metallic oxoanionic moiety.
ImidothioestersCHEMONTID:0001094Organic thioester derivatives of imidic acid. They have the general structure RSC(CR')=NR\", where R=organyl group, R'-R\"= H or organyl group.
EndocannabinoidsCHEMONTID:0001103Arachidonic acid derivatives containing either an N-acetylethanolamine(type 1) or a glycerol(types 2 and 3) moiety attached to the aliphatic tail.
Thiocarboxylic acids and derivativesCHEMONTID:0001112Organic compounds containing a derivative of thiocarboxylic acid, with the general structure RC(=S)R' (R=H, alkyl, aryl; R'=any heteroatom).
PyrimidodiazepinesCHEMONTID:0001132Compounds containing a pyrimidoazepine moiety, which consists of a pyrimidine fused to a piperazine ring by a bond. Pyrimidine is 6-membered ring consisting of five carbon atoms and two nitrogen atoms at ring positions 1 and 3. Diazepine is a 7-membered ring consisting of five carbon atoms and two nitrogen centers.
Nucleoside and nucleotide analoguesCHEMONTID:0003737Analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.
Harmala alkaloidsCHEMONTID:0001140Compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole.
Allyl-type 1,3-dipolar organic compoundsCHEMONTID:0003631Organic 1,3-dipolar compounds with the general structure X=Y+-Z- <-> X--Y+=Z<-> X+-Y-Z-<-> X-=Y-Z+ (X, Z = C, N, or O; Y = N or O).
Thiosulfinic acid estersCHEMONTID:0001161Organic compounds containing an ester of thiosulfinic acid with the general structure RS(=S)OR' (R, R'=alkyl, aryl).
Organic thiophosphonic acid derivativesCHEMONTID:0001163Organic compounds containing thiophosphonic acid functional group. Thiophosphonic acid is a phosphorus compound with the formula OP(O)(=S).
ThioacetalsCHEMONTID:0001187Organic compounds containing either the monothiacetal functional group (R2C(OR')(SR')) or the dithioacetal (R2C(SR')2) functional group .
ThiocyanatesCHEMONTID:0001201Salts or esters of thiocyanic acid, with the general formula RSC#N (R=alkyl, aryl).
ThioethersCHEMONTID:0001202Compounds containing the ester derivative of thiocarboxylic acid, with the general structure R-S-R' (R,R'=alkyl, aryl).
ThioureasCHEMONTID:0001209Organic compounds containing the thiourea functional group, a derivative of urea with the general structure (R1(N)R2C(=S)(R3)R4, R1-R4=H, alkyl, aryl), obtained by replacing the carbonyl group of urea with a thiocarbonyl group.
ThiolsCHEMONTID:0002485Organic compounds containing a functional group with the structure RSH (R = organyl).
ThiolactonesCHEMONTID:0001214Cyclic thioesters obtained by replacing the oxygen atom from a lactone ring with sulfur.
Organic thiophosphoric acids and derivativesCHEMONTID:0001303Organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure RP(R')(R'')=S, where R,R',R'' = O,N, halogen residue.
IsothioureasCHEMONTID:0001232Organic compounds containing the isothiourea group, with the general structure R1SC(=NR2)N(R3)R4 (R1,R2,R3,R4=H, alkyl, aryl).
IsothiocyanatesCHEMONTID:0001234Organic compounds containing the isothiocyanate group, an isocyanate analogue with the general formula RN=C=S.
Orthocarboxylic acid derivativesCHEMONTID:0001236Organic compounds containing the orhtocarboxylic acid functional group, with the RC(X)(X)X (R=H, alkyl, aryl; X=OH, alkoxy, aryloxy, substituted amino, etc.).
Organic fluorophosphonic acids and derivativesCHEMONTID:0001247Organic compounds containing fluorophosphonic acid or a derivative thereof.
Sulfinyl compoundsCHEMONTID:0003130Organic compounds containing a sulfinyl group with the general formula RS(=O)R' (R = organyl, R' = any atom but O).
Pyridine nucleotidesCHEMONTID:0001297Compounds containing a (deoxy)ribose phosphate with the ribose unit N-linked to a pyridine ring.
Miscellaneous mixed metal/non-metalsCHEMONTID:0001270Inorganic compounds containing non-metal as well as metal atoms but not belonging to afore mentioned classes.
Purine nucleotidesCHEMONTID:0001506Nucleotides with a purine base attached to the ribosyl moiety.
Pyrimidine nucleotidesCHEMONTID:0001509Nucleotides containing a pyrimidine base.
Brevetoxins and derivativesCHEMONTID:0001304A group of cyclic polyether compounds produced naturally by a species of dinoflagellate known as Karenia brevis. They contain a Pentaoxapentacycloheptacos- 23-en-7-one derivative (type a brevetoxin) or a pentaoxapentacyclotetracosa- 8,23-dien-7-one derivative (type b brevetoxin).
Organic hydroperoxidesCHEMONTID:0001308Organic compounds comprising the hydroperoxide functional group, with the general formula [O-O]2-.
Flavin nucleotidesCHEMONTID:0001329Nucleotides containing a flavin moiety. Flavin is a compound that contains the tricyclic isoalloxazine ring system, which bears 2 oxo groups at the 2- and 4-positions.
Inorganic sulfuryl halidesCHEMONTID:0001333Inorganic compounds containing the sulfuryl chloride functional group, with the general structure XS(R)(=O)=O (X=Br,Cl,F,I; R=hetero atom).
Intermetallic alkali metal compoundsCHEMONTID:0001360Inorganic compounds containing only metal atoms of at least two different types, where the heaviest atom is an alkali metal.
BenzodioxinsCHEMONTID:0002100Organic compounds containing a benzene ring fused to a dioxin ring. Dioxin a six-membered unsaturated ring of two oxygen atoms and four carbon atoms.
DioxinsCHEMONTID:0001384Compounds containing a dioxin ring, which is a six-membered unsaturated ring of two oxygen atoms and four carbon atoms.
SultimsCHEMONTID:0001387Tautomeric forms of sultams, having a sulfur-nitrogen double bond as part of a ring.
NeoflavonoidsCHEMONTID:0001614Compounds with a structure based on the 4-phenylchromene backbone.
ColchicinesCHEMONTID:0001390Compounds containing the benzo[a]heptalene based colchicin moiety or a derivative thereof. Colchicine is a tricyclic compound consisting of a benzene ring angularly fused to a tetrahydroheptalene that carries a N-acetamide group.
BenzoxazinesCHEMONTID:0001396Organic compounds containing a benzene fused to an oxazine ring (a six-membered aliphatic ring with four carbon atoms, one oxygen atom, and one nitrogen atom).
Imidazole ribonucleosides and ribonucleotidesCHEMONTID:0001997Organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. This class does not contain benzimidazole nucleosides and nucleotides.
Organothiophosphorus compoundsCHEMONTID:0001438Organic derivatives of thiophosphonic acid, thiophosphoric acid, dithiophosphoric acid, or phosphorotrithioic acid, or derivatives thereof. Thiophosphonic acid, dithiophosphoric acid, thiophosphoric acid, and phosphorotrithioic acid are thiophosphorus compounds with the formula OP(O)(=S), OP(S)(=S)O, OP(O)(=S)O, and OP(=S)(S)S, respectively.
TriazolopyrimidinesCHEMONTID:0001443Polycyclic aromatic compounds containing triazole ring fused to a pyrimidine ring. Triazole is a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
ThienoimidazolidinesCHEMONTID:0001446Heterocyclic compounds containing a thiophene ring fused to an imidazolidine ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Imidazolidine is 5-membered saturated ring of three carbon atoms, and two nitrogen centers at the 1- and 3-positions.
Intermetallic alkaline earth metal compoundsCHEMONTID:0001449Inorganic compounds containing only metal atoms of at least two different types, where the heaviest atom is a lanthanide.
Intermetallic lanthanide compoundsCHEMONTID:0001450Inorganic compounds containing only metal atoms of at least two different types, where the heaviest atom is lanthanide.
Intermetallic actinide compoundsCHEMONTID:0001451Inorganic compounds containing only metal atoms of at least two different types, where the heaviest atom is a actinide metal.
Intermetallic metalloid compoundsCHEMONTID:0001452Compounds containing only metal atoms of at least two different types, where the heaviest atom is a metalloid.
Intermetallic transition metal compoundsCHEMONTID:0001453Inorganic compounds containing only metal atoms of at least two different types, where the heaviest atom is a transition metal.
Intermetallic post-transition metal compoundsCHEMONTID:0001454Inorganic compounds containing only metal atoms of at least two different types, where the heaviest atom is a post-transition metal.
AnatoxinsCHEMONTID:0001465Organic compounds containing or derived from anatoxin, homoanatoxin or other analogues. Anatoxins constitute a class of potent neurotoxic alkaloids.
Epibatidine analoguesCHEMONTID:0001493Compounds containing an epibatidine moiety, with a structure characterized by a 2-chloropyridine moiety connected to an 7-azabicyclo[2.2.1]heptane in exo position.
Thiocarbamic acidsCHEMONTID:0001507Organic compounds containing a functional group with the general structure HOC(=S)N(R1)R2 (R=halogen; R1,R2=H, alkyl, aryl).
Organic oxoazanium compoundsCHEMONTID:0001508Organic compounds comprising the oxoazanium cation, with the formula N+=O.
Lignan glycosidesCHEMONTID:0001511Aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.
OrganoastatidesCHEMONTID:0001514Compounds containing a chemical bond between a carbon atom and an astatin atom.
OrganobromidesCHEMONTID:0001515Compounds containing a chemical bond between a carbon atom and a bromine atom.
OrganochloridesCHEMONTID:0001516Compounds containing a chemical bond between a carbon atom and a chlorine atom.
OrganofluoridesCHEMONTID:0001517Compounds containing a chemical bond between a carbon atom and a fluorine atom.
OrganoiodidesCHEMONTID:0001518Compounds containing a chemical bond between a carbon atom and an iodine atom.
SaccharolipidsCHEMONTID:0003918Compounds in which fatty acids are linked directly to a sugar backbone, forming structures that are compatible with membrane bilayers. In the saccharolipids, a sugar substitutes for the glycerol backbone that is present in glycerolipids and glycerophospholipids. The most familiar saccharolipids contain an acylated glucosamine. In contrast to others glycolipids, the fatty acid is not glycosidically linked to the sugar moiety.
Organo-post-transition metal compoundsCHEMONTID:0001523Organic compounds containing a post-transition metal atom.
PolysaccharidesCHEMONTID:0001539Compounds containing more than ten saccharide units.
Unsaturated hydrocarbonsCHEMONTID:0004475Hydrocarbons that contains one or more unsaturated carbon atoms. These compounds contain one or more double, triple, or aromatic bonds.
Pumiliotoxins, homopumiliotoxins, and allopumiliotoxinsCHEMONTID:0001567Neurotoxic alkaloids, containing a 8-methyl-octahydroindolizin-8-ol or 1-methyl-octahydro-1H-quinolizin-1-ol moiety.
Inorganic phosphorotrithioic acids and derivativesCHEMONTID:0001569Inorganic compounds containing a phosphorotrithioic acid group, with the structure OP(S)(S)=S (or SP(S)(S)=O).
QuinodimethanesCHEMONTID:0001579Compounds containing a cyclohexene or cyclohexadiene ring that bears two methylidene groups.
Furanoid lignansCHEMONTID:0003686Lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units.
Arylnaphthalene lignansCHEMONTID:0001610Lignans containing the arylnaphthalene skeleton, especially 9-(2H-1,3-benzodioxol-5-yl)-1H,3H-naphtho[2,3-c]furan-1-one or a derivative thereof. Arylnaphthalene lignans occur in nature and exhibit diverse biological activities.
Dibenzocyclooctadiene lignansCHEMONTID:0001623Compounds containing a dibenzocyclooctadiene moiety, which consists of two hydroxylated benzene connected by a cycloheptene ring.
Dibenzylbutane lignansCHEMONTID:0001969Lignan compounds containing a 2,3-dibenzylbutane moiety.
Aryltetralin lignansCHEMONTID:0003425Lignans with a structure based on the 1-phenyltetralin skeleton.
PhenanthrolinesCHEMONTID:0001626Aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring.
Linear 1,3-diarylpropanoidsCHEMONTID:0003467Organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together.
Aurone flavonoidsCHEMONTID:0001631Flavonoids containing a 2-Benzylidene-1-benzofuran-3-one based core. Aurone flavonoids provide the bright yellow color of some important ornamental flowers, such as snapdragon (Antirrhinum majus).
HomoisoflavonoidsCHEMONTID:0002507Naturally occurring oxygen heterocycles with a structure based on a 16-carbon skeleton including a chromanone, chromone or chromane system with a benzyl group at position C-3.
NaphthofuransCHEMONTID:0001634Compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.
NaphthopyransCHEMONTID:0001640Compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.
Depsides and depsidonesCHEMONTID:0001645Polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).
IsochromanequinonesCHEMONTID:0001649Polycyclic compounds containing an isochromanequinone, which is structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.
TroponesCHEMONTID:0001650Compounds containing a tropone ring, which is a cycloheptatrienone ring bearing a ketone group.
Thiohemiaminal derivativesCHEMONTID:0001666Compounds containing the thiohemiaminal group with the general structure R1SC(R2)(R3)N(R4)R5 (R1-R5=H, alkyl, aryl).
Acyclic allenesCHEMONTID:0001678Acyclic hydrocarbons (and by extension, derivatives formed by substitution) having two double bonds from one carbon atom to two others.
Cyclic allenesCHEMONTID:0001679Cyclic hydrocarbons (and by extension, derivatives formed by substitution) having two double bonds from one carbon atom to two others.
OxepanesCHEMONTID:0001729Compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.
PiperidinylpyridinesCHEMONTID:0001730Compounds containing a piperidinylpyridine moiety, which consists of a piperidine linked to a pyridine by a single bond that is not pat of a ring.
KavalactonesCHEMONTID:0001761Lactones, which is structurally characterized by a benzene ring and a pyranone moiety, linked to each other to form a 4-methoxy-6-(2-phenylethyl)-2H-pyran-2-one skeleton.
Amaryllidaceae alkaloidsCHEMONTID:0001775Isoquinoline alkaloids with a skeleton deriving from lycorine, norbelladine, homolycorine, hemanthamine, crinine, tazettine, montanine, plicamine, galanthindole, galanthamine, gracilline, among others. Amaryllidaceae Alkaloids represent a large group of biogenetically related isoquinoline alkaloids that are found exclusively in plants belonging to this family of Amaryllidaceae. This group of alkaloids is also derived from two tyrosine units which combine, with loss of one carbon atom, to give a benzylphenylethylamine precursor unit, e.g. Norbelladine, which by various oxidative cyclisation processes, prominent among which are phenol oxidative coupling reactions, can give rise to the nine major skeletal groups.
Erythrina alkaloidsCHEMONTID:0001782Organic compounds with a structure based on a backbone containing a indole-6-ol sharing its nitrogen atom with an isoquinoline ring system.
Curan alkaloidsCHEMONTID:0001783Compounds containing the pentacyclic curan skeleton, which is structurally characterized by the presence of a pentacyclic 3,5-ethanopyrrolo[2,3-d]carbazole framework.
ThiaergolinesCHEMONTID:0001784Ergoline analogues, obtained by replacing the oxygen atom in the indole moiety (of the ergoline backbone) by a sulfur atom.
OxamorphinansCHEMONTID:0001785Polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated naphthopyran moiety, one of which is aromatic while the two others are alicyclic.
Yohimbine alkaloidsCHEMONTID:0001786Alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor.
Ochratoxins and related substancesCHEMONTID:0001787A group of chemically related metabolites containing a 3,4-dihydro-3-methylisocoumarin moiety linked through a carboxyl group to L-beta-phenylalanine by a secondary amine bond.
Ellipticine alkaloidsCHEMONTID:0001793Compounds containing a pyrido[4,3-b]carbazole moiety.
Ajmaline-sarpagine alkaloidsCHEMONTID:0001794Organic compounds containing either of the ajmalan, sarpagan skeleton, or derivative thereof. The Sarpagine (Akuammidine) group, based on the sarpagan nucleus, arises from bond formation between C-16 and C-5 of the corynantheine precursor. Ajmaline alkaloids are based on a 17,19-secoyohimban skeleton (oxayohimban) which is invariably present as an ether.
Lupin alkaloidsCHEMONTID:0002719Alkaloids extracted from the lupinus species. They usually possess a bi-, tri-, or tetracyclic skeleton consisting of one or more quinolizidine moieties.
OxocinsCHEMONTID:0001796Compounds containing an oxocin ring, which is a eight-member unsaturated aromatic ring containing one oxygen atom and seven carbon atoms.
PyrrolotriazinesCHEMONTID:0001798Compounds containing a pyrrolotriazine moiety, which consists of a pyrrole ring fused to a triazine ring. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Triazine is a 6-membered ring consisting of three carbon atoms and three nitrogen centers.
PyrrolopyrimidinesCHEMONTID:0001799Compounds containing a pyrrolopyrimidine moiety, which consists of a pyrrole ring fused to a pyrimidine. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
Saxitoxins, gonyautoxins, and derivativesCHEMONTID:0001800Compounds with a structure based on a 2,6-diamino-4-methyl-pyrrolo[1,2-c]purin-10-ol skeleton.
Okadaic acids and derivativesCHEMONTID:0001802Marine heterocyclic polyethers containing the okadaic acid skeleton.
Ciguatera toxinsCHEMONTID:0001808Lipid-soluble polyether compounds consisting of 13 to 14 rings fused by ether linkages into a most rigid ladder-like structure.
FurofuransCHEMONTID:0001816Organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.
SterigmatocystinsCHEMONTID:0001817A group of closely related fungal metabolites chemically characterized by a xanthone moiety fused to a dihydrodifurano or a tetrahydrodifurano moiety. The chemical difference among the various sterigmagocystins are the presence or absence of unsaturation at positions 2 and 3 of the difurano ring system, the substitution pattern on positions 6, 7, and 10 of the xanthone system and/or the substituent on position 3 of the difurano system. They are produced by Aspergilus spp. and Bipolaris spp.
FuropyransCHEMONTID:0001818Organic polycyclic compounds containing a furan ring fused to a pyran ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.
CytochalasansCHEMONTID:0001821Fungal metabolites structurally characterized by the presence of an isoindolone nucleus fused to a macrocyclic ring, which can either a lactone, as in cytochalasin B, a carbonate, as in cytochalasin E, or a carbocycle, as in cytochalasin D, H, and K.
ThienopyrrolesCHEMONTID:0001833Heterocyclic compounds containing a thiophene ring fused to a pyrrole ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom.
PyrrolothiazolesCHEMONTID:0001834Compounds containing a pyrrolothiazole moiety, which consists of a pyrrole ring fused to a thiazole ring. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Thiazole is a 6-membered ring that contains both sulfur and nitrogen.
FlavonolignansCHEMONTID:0001844Non-conventional lignans that derived from flavonoids. They are characterized by a p-dioxin ring substituted at one carbon atom by a C3C6 (phenylpropan) group and fused to the B-ring of the 2-phenylchromene moiety.
ThiophenolsCHEMONTID:0001850Compounds containing a thiophenol ring, which a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom.
TrioxanesCHEMONTID:0001853Compounds containing a six-member aliphatic saturated heterocycle made up of three oxygen atoms and three carbon atoms.
TrioxolanesCHEMONTID:0001854Compounds containing a five-member aliphatic saturated heterocycle made up of three oxygen atoms and two carbon atoms.
DiazanaphthalenesCHEMONTID:0004788Aromatic heterocyclic chemical compounds containing a naphthalene derivative, where two carbon atoms are replaced by nitrogen atoms. They are subdivided in benzodiazines and naphthyridines.
PyridopyrimidinesCHEMONTID:0001859Compounds containing a pyridopyrimidine, which consists of a pyridine fused to a pyrimidine. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
TrithianesCHEMONTID:0001862Organic compounds containing a six-member aliphatic saturated heterocycle made up of three sulfur atoms and three carbon atoms.
DithianesCHEMONTID:0001863Compounds containing a dithiane moiety, which is composed of a cyclohexane core structure wherein two methylene units are replaced by sulfur centres.
Benzotriazole ribonucleosides and ribonucleotidesCHEMONTID:0001867Nucleosides with a structure that consists of an imidazole moiety of benzotriazole is N-linked to a ribose (or deoxyribose). Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Indazole ribonucleosides and ribonucleotidesCHEMONTID:0001868Compounds in which the C-1 of a ribose (or deoxyribose) is linked to the N1-position of the indazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Indole ribonucleosides and ribonucleotidesCHEMONTID:0001869Compounds in which the C-1 of a ribosyl (or deoxyribosyl) moiety is linked to the N1-position of an indole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
BenzoxathiolesCHEMONTID:0001875Organic compounds containing a benzene fused to an oxathiole ring (a five-membered ring with four carbon atoms, one oxygen atom, and one sulfur atom).
ThiazetidinesCHEMONTID:0001881Heterocyclic compounds containing a saturated four-member ring with two carbon atoms, one sulfur atom, and one nitrogen.
ThiazinanesCHEMONTID:0001884Heterocyclic compounds containing a saturated six-member ring with four carbon atoms, one sulfur atom, and one nitrogen.
OxathietanesCHEMONTID:0001886Compounds containing an oxathietane moiety, which consists of a saturated aliphatic four-member ring with one oxygen atom, a sulfur atom, and two carbon atoms. Isomers of oxaphospholane include 1,2-oxathietane, and 1,3-oxathietane.
OxathianesCHEMONTID:0001889Compounds containing an oxathiane moiety, which consists of a saturated aliphatic six-member ring with one oxygen atom, a sulfur atom, and four carbon atoms. Isomers of oxaphospholane include 1,2-oxathiane, 1,3-oxathiane,and 1,4-oxathiane.
Isocoumarins and derivativesCHEMONTID:0001890Polycyclic compounds containing an isochromane which bears a ketone at the carbon C1.
ThianesCHEMONTID:0001894Heterocyclic compounds containing a saturated six-member ring with five carbon atoms and one sulfur atom.
ThiopyransCHEMONTID:0001895Compounds containing a six-member aliphatic heterocycle made up of one sulfur atom and five carbon atoms.
Macrolide lactamsCHEMONTID:0001900Cyclic polyketides containing both a cyclic amide and a cyclic ester group.
Protoberberine alkaloids and derivativesCHEMONTID:0001909Alkaloids with a structure based on a protoberberine moiety, which consists of a 5,6-dihydrodibenzene moiety fused to a quinolizinium and forming 5,6-Dihydrodibenzo(a,g)quinolizinium skeleton.
BenzoxepinesCHEMONTID:0001910Organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom).
FuropyrrolesCHEMONTID:0001918Organic polycyclic compounds containing a furan ring fused to a pyrrole ring. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom.
ThienothiazinesCHEMONTID:0001928Heterocyclic compounds containing a thiophene ring fused to a thiazine. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Thiazine is a 6-membered ring consisting of four carbon, one nitrogen and one sulfur atoms.
ThienothiazolesCHEMONTID:0001929Heterocyclic compounds containing a thiophene ring fused to a thiazole. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Thiazole is a 6-membered ring that contains both sulfur and nitrogen.
BenzoxadiazolesCHEMONTID:0001930Organic compounds containing a benzene fused to an oxadiazole ring (a five-membered ring with two carbon atoms, one nitrogen atom, and one oxygen atom).
ThienopyransCHEMONTID:0001965Heterocyclic compounds containing a thiophene ring fused to a pyran ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.
OxolanesCHEMONTID:0001967Organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms.
ImidazodiazepinesCHEMONTID:0001979Organic compounds containing an imidazole ring fused to a diazepine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Diazepine is a 7-membered ring consisting of five carbon and two nitrogen atoms.
Glycero-3-dithiophosphocholinesCHEMONTID:0001980Glycerolipids in which the glycerol moiety is esterified at two positions with a fatty acyl chain, and linked a third position (O3) with a dithiophosphocholine.
Glycero-3-thiophosphocholinesCHEMONTID:0001981Glycerolipids in which the glycerol moiety is esterified at two positions with a fatty acyl chain, and linked a third position (O3) with a thiophosphocholine.
DihydrofuransCHEMONTID:0001983Compounds containing a dihydrofuran moiety, which is a furan derivative with only one double bond.
DioxolopyransCHEMONTID:0001985Compounds containing a dioxolopyran moiety, which consists of a dioxole ring fused to a pyran ring.
PyrroloazepinesCHEMONTID:0001990Compounds containing a pyrroloazepine moiety, which is a bicyclic heterocycle which consists of a pyrrole ring fused to an azepine. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Azepine is a 7-membered ring consisting of six carbon and one nitrogen atom.
PiperazinoazepinesCHEMONTID:0002000Compounds containing a piperazinoazepine skeleton, which consists of an azepine ring fused to a piperazine.
ImidazotetrazinesCHEMONTID:0002001Organic polycyclic compounds containing an imidazole ring fused to a tetrazine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Tetrazine is a six-membered aromatic heterocycle made up of four nitrogen atoms and a two carbon atoms.
PyrazolotriazinesCHEMONTID:0002005Compounds containing a pyrazolotriazine skeleton, which consists of a pyrazole fused to a triazine. Pyrazole is 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers. Triazine is a 6-membered ring consisting of three carbon atoms and three nitrogen centers.
PyranodioxinsCHEMONTID:0002011Polycyclic compounds containing a pyranodioxin moiety, which consists of a pyran ring fused to a dioxin ring.
OxanesCHEMONTID:0002012Compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.
ThienopyrimidinesCHEMONTID:0002020Heterocyclic compounds containing a thiophene ring fused to a pyrimidine ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
Bi- and oligothiophenesCHEMONTID:0002021Organic compounds containing two or more linked thiophene rings. Thiophene is a five-member aromatic ring with one sulfur and four carbon atoms.
Seleninic acids and derivativesCHEMONTID:0002027Compounds containing a seleninic acid moiety, with the general structure RSe(=O)OH.
Organic thiosulfuric acids and derivativesCHEMONTID:0002035Organic compounds containing the thiosulfuric acid functional group or a derivative thereof.
TetrathianesCHEMONTID:0002050Organic compounds containing a tetrathiane ring, which is a six-member saturated aliphatic ring made up of four sulfur atoms and two carbon atoms.
DithiinsCHEMONTID:0002055Compounds comprising a dithiin ring, which is an unsaturated six-member heterocycle containing four carbon atoms, two sulfur atoms and two double bonds.
OxathiinsCHEMONTID:0002058Compounds containing an oxathiin moiety, which consists of an unsaturated aliphatic six-member ring with one oxygen atom, a sulfur atom, and four carbon atoms. Isomers of oxaphospholane include 1,2-oxathiin, 1,3-oxathiin,and 1,4-oxathiin.
BenzoxathiinsCHEMONTID:0002059Organic compounds containing a benzene fused to an oxathiin ring (a six-membered aliphatic ring with four carbon atoms, one oxygen atom, and one sulfur atom).
DiazaphospholanesCHEMONTID:0002061Cyclic organic compounds containing a five-member aliphatic single-bonded ring, with a phosphorine atom and two nitrogen atoms at the ring positions 1, 2, and 3 respectively.
DiazaphospholinesCHEMONTID:0002062Cyclic organic compounds containing a five-member aliphatic unsaturated ring with only double bond, and with a phosphorine atom, two nitrogen atoms at the ring positions 1, 2, and 3 respectively.
DiazaphospholesCHEMONTID:0002063Cyclic organic compounds containing a five-member aliphatic unsaturated ring with two double bonds, and with a phosphorine atom, two nitrogen atoms at the ring positions 1, 2, and 3 respectively.
HistrionicotoxinsCHEMONTID:0002064Frog toxins structurally characterized by the presence of a dodecahydropyrrolo[1,2-a]quinolin-1-yl}ethanol moiety or a 2,7-disubstituted 1-azaspiro[5.5]undecan-8-ol moiety.
DithiolesCHEMONTID:0002090Compounds comprising a dithiole ring, which is an unsaturated five-member heterocycle containing three carbon atoms, two sulfur atoms and a double bond.
DihydrothiophenesCHEMONTID:0002091Compounds containing a dihydrothiophene moiety, which is a thiophene derivative with only one double bond.
AnthracyclinesCHEMONTID:0002106Polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage.
DioxiranesCHEMONTID:0002109Compounds containing a three-membered cyclic with two oxygen atoms and a carbon atom.
PyranopyridinesCHEMONTID:0002111Polycyclic aromatic compounds containing a pyran ring fused to a pyridine ring.
NaphthothiazolesCHEMONTID:0002114Polycyclic aromatic compounds containing a thiazole fused to a naphthalene. Thiazole is a 5-membered aromatic ring containing three carbon, one oxygen, and one nitrogen atom. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.
TriazolopyridazinesCHEMONTID:0002117Polycyclic compounds containing a triazole fused to a pyridazine. Triazole is a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Pyridazine is a six-membered aromatic ring with two adjacent nitrogen atoms, and for carbon atoms.
OxazolopyridinesCHEMONTID:0002118Polycyclic compounds containing an oxazole ring fused to a pyridine ring.
TriazolothiazolesCHEMONTID:0002124Polycyclic compounds containing a triazole ring fused to a thiazole ring. Triazole is a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Thiazole is a 6-membered ring that contains both sulfur and nitrogen.
PyrazolopyrazolesCHEMONTID:0002127Polycyclic aromatic compounds containing to pyrazole rings fused to each other. Pyrazole is 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers.
PyrrolopyrazolesCHEMONTID:0002128Polycyclic aromatic compounds containing a pyrrole fused to a pyrazole ring. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Pyrazole is a 5-membered ring consisting of three carbon atoms and two adjacent nitrogen centers.
PyranopyrimidinesCHEMONTID:0002129Polycyclic aromatic compounds containing a pyran ring fused to a pyrimidine ring.
10,11-secoergolinesCHEMONTID:0002164Ergoline derivatives, where carbon atoms C10 and C11 of the ergoline moiety are not linked to each other.
Pyrazole ribonucleosides and ribonucleotidesCHEMONTID:0002174Nucleosides and nucleotides containing a pyrazole moiety is linked to a ribose (or ribose derivative).
Pyrazolopyrimidine ribonucleosides and ribonucleotidesCHEMONTID:0002185Nucleoside or nucleotide analogues containing a pyrazolopyrimidine moiety is N-linked to a ribose (or ribose derivative). Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Phthalide isoquinolinesCHEMONTID:0002188Organic compounds with a structure characterized by an isoquinoline moiety linked to phthalide.
TetrahydroisoquinolinesCHEMONTID:0002955Tetrahydrogenated isoquinoline derivatives.
6,7-secoergolinesCHEMONTID:0002192Compounds containing a tricyclic ergoline analog, where carbon atoms C6 and C7 are not linked to each other.
OxazolopyrazinesCHEMONTID:0002197Polycyclic compounds containing an oxazole ring fused to a pyrazine ring.
DioxaborolanesCHEMONTID:0002225Compounds containing a five-member saturated aliphatic heterocycle made up of two oxygen atoms, a boron atom, and three carbon atoms.
DioxaborolesCHEMONTID:0002226Compounds containing a five-member unsaturated aliphatic heterocycle made up of two oxygen atoms, a boron atom, and three carbon atoms.
Cinchona alkaloidsCHEMONTID:0002246Alkaloids structurally characterized by the presence of the cinchonan skeleton, which consists of a quinoline linked to an azabicyclo[2.2.2]octane moiety.
OxathiolesCHEMONTID:0002261Organic heterocyclic compounds containing a saturated five-membered ring with three carbon atoms, one oxygen atom, one sulfur atom, and one double bond.
Pyrrolopyrimidine nucleosides and nucleotidesCHEMONTID:0002306Nucleoside derivatives containing a ribose derivative which is n-glycosylated to a pyrrolopyrimidine. Also called deazapurine nucleosides, they are analogs of purine nucleosides with the N atom of the purine being replaced by a C atom at position 7.
ThienodiazepinesCHEMONTID:0002313Heteropolycyclic containing a thiophene ring fused to a diazepine ring. Thiophene is 5-membered ring consisting of four carbon and one sulfur atoms. Diazepine is a 7-membered ring consisting of five carbon and two nitrogen atoms.
Phenol estersCHEMONTID:0002319Aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group.
TriazolodiazepinesCHEMONTID:0002322Heterocyclic aromatic compounds containing a triazole ring fused to a diazepine ring. Triazole is a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Diazepine is a 7-membered ring consisting of five carbon and two nitrogen atoms.
BenzothiadiazolesCHEMONTID:0002323Heterocyclic aromatic compounds containing a benzene ring fused to a thiadiazole ring. Thiadiazole is a five-membered aromatic heterocycle made up of one sulfur atom and two nitrogen atoms.
IsoxazolopyridinesCHEMONTID:0002330Aromatic compounds containing an isoxazole ring fused to a pyridine ring. Isoxazole is five-membered ring with three carbon atoms, and an oxygen atom next to a nitrogen atom. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center.
IsoxazolopyrazinesCHEMONTID:0002331Aromatic compounds containing an isoxazole ring fused to a pyrazine ring. Isoxazole is five-membered ring with three carbon atoms, and an oxygen atom next to a nitrogen atom. Pyrazine is a 6-membered ring consisting of six carbon atoms and two nitrogen centers at ring positions 1 and 4.
BenzisoxazolesCHEMONTID:0002332Aromatic compounds containing a benzene ring fused to an isoxazole ring. Isoxazole is five-membered ring with three carbon atoms, and an oxygen atom next to a nitrogen atom.
CycloheptathiophenesCHEMONTID:0002338Polycyclic compounds containing a thiophene ring fused to a 7 member carbocyclic moiety. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom.
Triazole ribonucleosides and ribonucleotidesCHEMONTID:0002342Nucleoside derivatives containing a ribose (or deoxyribose) moiety which is N-glycosylated to a triazole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
BenzocycloheptapyridinesCHEMONTID:0002351Aromatic compounds containing a benzene ring and a pyridine ring fused to a seven membered carbocycle.
ThioenolsCHEMONTID:0002353Compounds containing the enol functional group, with the structure HS(R)C=CR'. Thioenols interconvert with thioketones that have an alpha-hydrogen.
Thiophenol ethersCHEMONTID:0002359Thioether derivatives of thiophenols. Thiophenol is a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom.
Thiophenol estersCHEMONTID:0002360Thioester derivatives of thiophenols. Thiophenol is a phenol derivative obtained by replacing the oxygen atom from the hydroxyl group (attached to the benzene) by a sulfur atom.
PiperazinopiperidinesCHEMONTID:0002377Organic aromatic compounds containing a piperazine ring fused to a piperidine.
Thiophthalic anhydridesCHEMONTID:0002401Organic heterocyclic aromatic compounds that contain a 1,3-dihydro-2-benzothiophene-1,3-dione moiety.
Carboselenoic acids and derivativesCHEMONTID:0002427Organic compounds containing at least one carboselenoyl group, with the formula RC(=O)Se (or a derivative thereof).
Propargyl-type 1,3-dipolar organic compoundsCHEMONTID:0003633Organic 1,3-dipolar compounds with the general structure X#N+-Z- <-> X-=N+=Z <-> X-=N-Z+ <-> X-N=Z (X = C or O, Z = C, N, or O).
Imidothioic acids and derivativesCHEMONTID:0002462Sulfur derivatives of imidic acid (a derivatives thereof) containing the functional group -RC(=N)S, obtained by replacing the oxygen atom by a sulfur atom.
OxazaphosphinanesCHEMONTID:0002466Organic heterocyclic compounds containing an oxazaphosphinane ring, which consists of three carbon atoms, one nitrogen atom, and one phosphorus atom.
Perselenic acids and derivativesCHEMONTID:0002475Compounds containing a P-hydrocarbyl derivative of perselenic acid (or a derivative thereof).
Telluric acids and derivativesCHEMONTID:0002480Organic acids containing a telluric acid group or a derivative thereof.
DioxathiolanesCHEMONTID:0002486Organic heterocyclic compounds containing a dioxathiolane, with a structure consisting of a five-membered saturated ring with one sulfur atom, two oxygen atoms, and two carbon atoms.
OligophosphenesCHEMONTID:0002488Organophosphorus compounds with the general formula RP=P-PR' (R=alkyl, aryl).
DiphosphenesCHEMONTID:0002489Organophosphorus compounds with the general formula RP=PR'(R,R'= alkyl, aryl).
IsothiochromenesCHEMONTID:0002498Organic heterocyclic compounds containing an isothiochromene moiety.
ThiochromenesCHEMONTID:0002499Organosulfur compounds that are analogues to chromene, with the difference that a sulfur atom replaces the oxygen atom.
HalohydrinsCHEMONTID:0002528Alcohols substituted by a halogen atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups (usually used to mean beta-halo alcohols).
EpoxypiperidinesCHEMONTID:0002530Heteropolycyclic compounds containing an oxirane fused to a piperidine ring.
Thiosulfonimidic o-acidsCHEMONTID:0002531Organic compounds with the general formula HOS(R)(=N)(=S) (R = alkyl, aryl).
Thiosulfonimidic s-acidsCHEMONTID:0002532Organic compounds with the general formula HSS(R)(=N)(=O) (R = alkyl, aryl).
Trithiosulfonic acidsCHEMONTID:0002533Organic compounds with the general formula HSS(R)(=S)(=S) (R = alkyl, aryl).
Sulfinohydroximic acidsCHEMONTID:0002534Organic compounds with the general formula HON=S(R)OH.
Sulfinohydrazonic acidsCHEMONTID:0002535Organic acids with the general formula RS(=NN)OH.
Nitronic acidsCHEMONTID:0002538Organic compounds containing the nitronate functional group with the general formula RC=N+(O)OH or RCN+(=O)OH.
DihydroxyphosphanesCHEMONTID:0002540Organic compounds with the general formula RP(OH)OH.
Carbodithioic acidsCHEMONTID:0002541Organic acids with the general formula RC(=S)SH (R = organyl).
Dithiosulfonic O-acidsCHEMONTID:0002543Organic acids with the general formula RS(=S)(=S)OH.
Dithiosulfonic S-acidsCHEMONTID:0002544Organic acids with the general formula RS(=O)(=S)SH.
CoumarinolignansCHEMONTID:0002545Lignans with a structure characterized by the presence of a 1,4-dioxane bridge substituted by a phenyl group, and fused to a coumarin.
DiazetidinesCHEMONTID:0002546Organic compounds containing the diazetidine ring, a saturated four-membered ring with two nitrogen atoms and 2 carbon atoms.
Phenylpropanoic acidsCHEMONTID:0002551Compounds with a structure containing a benzene ring conjugated to a propanoic acid.
ThiatriazolesCHEMONTID:0002561Heteroaromatic compounds containing a thiatriazole ring, which is a five-membered aromatic ring with one sulfur atom, three nitrogen atom, and a carbon atom.
OxathiazolidinesCHEMONTID:0002578Heterocyclic compounds containing an oxathiazolidine, a saturated five-membered ring having two carbon atoms, one oxygen atom, one nitrogen atom, and one sulfur atom.
Alpha-methyldeoxybenzoin flavonoidsCHEMONTID:0002612Flavonoids with a structure based on a 1,2-diphenyl-2-propan-2-one.
ImidazopiperidinesCHEMONTID:0002627Heterocyclic compounds containing an imidazole ring fused to a piperidine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Piperidine is a five-membered heterocycle containing five carbon atoms and one nitrogen atom.
3,4-dihydrocoumarinsCHEMONTID:00026423,4-dihydrogenated coumarins. Coumarin is a bicyclic compound that a 1-benzopyran carrying an oxo group at the 2-position.
TetrahydrofuransCHEMONTID:0002648Heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.
OxathiaphospholanesCHEMONTID:0002649Heterocyclic compounds containing an oxathiophospholane ring, which is a saturated, five-membered ring with one oxygen atom, one sulfur atom, one phosphorus atom and two carbon atoms.
DiarylheptanoidsCHEMONTID:0002650Phenylpropanoids with a structure containing two aromatic rings joined by a seven carbons (a 1,7-diphenylheptane skeleton) and may have various substituents.
PhenalenesCHEMONTID:0002653Aromatic hydrocarbons containing a cyclohexene ring fused to both benzenes of a naphthalene ring system, so as to form a triad.
PhenalanesCHEMONTID:0002655Aromatic hydrocarbons containing a cyclohexene ring fused to both benzenes of a naphthalene ring system, so as to form a triad.
Loline alkaloids and derivativesCHEMONTID:0002656Alkaloids with a structure characterized by a saturated pyrrolizidine ring, a primary amine at the C-1 carbon, and an internal ether bridge joining two distant ring (C-2 and C-7) carbons. Different substituents at the C-1 amine, such as methyl, formyl, and acetyl groups, yield various loline species.
Cularin alkaloids and derivativesCHEMONTID:0002657Derivatives of benzyl isoquinolines in which a phenolic oxygen is incorporated into a seven-membered ring.
Rhoeadine alkaloidsCHEMONTID:0002658Alkaloids with a structure based on rhoeadine. They usually contain a benzazepine system fused with a six-membered hemiacetal or acetal.
Emetine alkaloidsCHEMONTID:0002659Alkaloids with a structure characterized by the presence of both an isoquinoline and a benzoquinolizidine nuclei.
ProaporphinesCHEMONTID:0002660Benzylisoquinoline derivatives characterized by the presence of a spirocyclohexane ring that can occur in various oxidation levels, from cyclohexadienone to cyclohexanol.
HomoaporphinesCHEMONTID:0002661Alkaloids derived from phenethylisoquinoline precursors by direct intramolecular oxidative coupling. They incorporate a nucleus A and are always pentaoxygenated at C- 1, -2, - 10, - 11, and - 12. The nitrogen function in ring B is usually N-methylated, but it may also be secondary.
HomoproaporphinesCHEMONTID:0002662Analogues of proaporphines with the difference that the spirocyclohexenol ring is joined to a cyclohexane instead of a cyclopentane.
AristolactamsCHEMONTID:0002663Phenanthrenic compounds containing a five-membered lactam ring and a 1,3-dioxolane ring fused to the phenanthrene ring system.
Benzophenanthridine alkaloidsCHEMONTID:0002665Polycyclic alkaloids with a structure based on the benzo[c]phenanthridine skeleton. They derived from tetrahydroprotoberberine precursors by oxidation of the C6-N bond followed by cyclisation of C6 on to position 13.
Eburnan-type alkaloidsCHEMONTID:0002671Alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.
Plumeran-type alkaloidsCHEMONTID:0002672Alkaloids with a structure based on the plumeran skeleton. Plumeran is a pentacyclic compound that consists of a pyrrolidine ring shed to the quinoline moiety of pyrido[3,2-c]carbazole ring system.
ThiirenesCHEMONTID:0002675Compounds containing a thriirene ring, an unsaturated three-membered ring made up of two carbon atoms and a sulfur atom.
Ergoline and derivativesCHEMONTID:0002679Compounds containing an ergoline moiety, which is structurally characterized by he presence of a 4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg] quinoline.
OxaergolinesCHEMONTID:0002681Alkaloids with a structure based on the oxaergoline skeleton, an analog of ergoline obtained by substituted one of the pyridine C atom by an oxygen atom.
DiazirinesCHEMONTID:0002691Heterocyclic compounds containing a diazirine ring, which is a three-membered unsaturated cycle with one carbon atom, and two nitrogen atoms joined by a double bond.
TriazirinesCHEMONTID:0002692Heterocyclic compounds containing a triazirine ring, which is a three-membered unsaturated cycle with three nitrogen atoms.
TriazinanesCHEMONTID:0002693Compounds containing a triazinane ring, which is a six-membered saturated heterocycle with three nitrogen ring atoms and three ring carbon atoms.
BenzodioxanesCHEMONTID:0002699Heterocyclic compounds containing a benzene ring fused to a dioxane ring. Dioxane a six-member saturated ring of two oxygen atoms and four carbon atoms.
Protopine alkaloidsCHEMONTID:0002743Alkaloids with a structure based on a tricyclic protopine formed by oxidative ring fission of protoberberine N-metho salts.
Vobasan alkaloidsCHEMONTID:0002744Alkaloids containing the vobasan skeleton.
Ibogan-type alkaloidsCHEMONTID:0002748Indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond.
Strychnos alkaloidsCHEMONTID:0002749Alkaloids having a core structure based on the strychnan, stemmadenine (seco-curan), or the akuammicine (curan) skeleton.
Corynanthean-type alkaloidsCHEMONTID:0002750Alkaloids with a structure based on the corynanthean nucleus, which is a tetracycle characterized by an indole fused to a quinolizidine. Additionally, the quinolizidine ring system is substituted to a 2-methylpropyl group and one ethyl group.
Vallesiachotaman alkaloidsCHEMONTID:0002751Alkaloids with a structure based on the vallesiachotaman skeleton. Vallesiachotaman is a tetracyclic compound that has a indolo[2,3-a]quinolizine core substituted by two methyl groups at the 3-, and 12-positions as well as a 2-methylbutane group at the 2-position.
Vincosan alkaloidsCHEMONTID:0002752Alkaloids containing the vincosan skeleton, a tetracyclic ring system containing a carboline and a tetrahydropyran ring.
Cinnamyl alcoholsCHEMONTID:0002754Aromatic alcohols containing a 3-phenylprop-2-en-1-ol moiety.
Aspidospermatan-type alkaloidsCHEMONTID:0002755Tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids.
Vinca alkaloidsCHEMONTID:0002756Alkaloids with a dimeric chemical structure composed of an indole nucleus (catharanthine), and a dihydroindole nucleus (vindoline), joined together.
Quebrachamine alkaloidsCHEMONTID:0002757Alkaloids with a structure based on the quebrachamine skeleton, a tetracyclic compound that is derived by fission of the 7,21 bond of the aspidospermidine skeleton. Some quebrachamine alkaloids lack the C-16 methoxycarbonyl group.
Rhazinilam alkaloidsCHEMONTID:0002758Alkaloids with a structure based on the rhazinilam skeleton, a tetracyclic compound with a complex tetracyclic carbon skeleton containing pyrrole ring embedded in its indolizine core.
Tacaman alkaloidsCHEMONTID:0002759Alkaloids containing the pentacyclic tacaman skeleton, which consists of a pyrido[1,2-a]indole fused to a quinolizine. Tacaman alkaloids are obtained from a precursor to a pseudoaspidospermidine (type II skeleton) derivative, by the formation of new bonds at C-20/C-3 and C-140/C-17.
PyridodiazepinesCHEMONTID:0002782Heterocyclic compounds containing a pyridine fused to a diazepine ring. Pyridine is 6-membered ring consisting of five carbon atoms and a nitrogen atom. Diazepine is a 7-membered ring consisting of five carbon atoms and two nitrogen centers.
Akuammilan and related alkaloidsCHEMONTID:0002783Alkaloids with a structure based on either the akuammilan skeleton. The ring system in this group is formed from a precursor of the corynantheine type by bond formation between C-16 and C-7. Variations in this subgroup include, among others, alkaloids derived by C-3 to N-4 bond fission, as well as alkaloids in which the N-4 to C-5 bond in the Akuammiline skeleton has been severed.
Acutumine and related alkaloidsCHEMONTID:0002791Alkaloids with a structure based on the tricyclic acutumine skeleton, which contains an indoline moiety and two cyclopentene rings.
Hasubanan alkaloidsCHEMONTID:0002792Alkaloids with a structure based on the hasubanan skeleton, a tetracyclic propellane.
Pavine alkaloidsCHEMONTID:0002793Alkaloids with a structure based on the pavine skeleton.
Isopavine alkaloidsCHEMONTID:0002794Alkaloids with a structure based on the isopavine skeleton.
Organic trisulfidesCHEMONTID:0002799Organosulfur compounds with the general formula RSSSR' (R,R'=alkyl, aryl).
Organic disulfidesCHEMONTID:0002800Organosulfur compounds with the general formula RSSR' (R,R' = alkyl, aryl).
BenzodithiinsCHEMONTID:0002804Organic heterocyclic compounds containing a benzene ring fused to a dithiin ring. Dithiin is an unsaturated six-member heterocycle containing four carbon atoms, two sulfur atoms and two double bonds.
9b-azaphenalenesCHEMONTID:0002824Alkaloids with a structure based on the perhydro-9b-azaphenalene skeleton. Perhydro-9b-azaphenalene is a tricyclic compound consisting of quinolizidine that share its only nitrogen atom with a piperidine. In some 9b-azaphenalenes, the resulting tricyclic backbone can be unsaturated.
ThiochromanesCHEMONTID:0002834Organic heterocyclic compounds containing a thiochromane moiety.
IsothiochromanesCHEMONTID:0002835Organic heterocyclic compounds containing an isothiochromane moiety.
LactimsCHEMONTID:0002854Cyclic amides of carboximidic acids. Lactams are tautomers of lactams, having an endocyclic carbon-nitrogen double bond.
Phosphorus mustard compoundsCHEMONTID:0002855Compounds having two beta-haloalkyl groups bound to a phosphorus atom.
Vinyl halidesCHEMONTID:0002868Organic compounds in which the halogen atom is bonded to an sp2-hybridised carbon atom of a carbon-carbon double bond (C=C).
Sulfinohydrazonoperoxoic acidsCHEMONTID:0002899Organic acids with the general formula RS(=NN)OOH.
1,2-diaryl-2-propen-1-olsCHEMONTID:0002900Flavonoids with a structure based on the 1,2-diaryl-2-propen-1-ol skeleton.
PerylenequinonesCHEMONTID:0002903Heterocyclic compounds characterized by two 8-hydroxy-1,4-dihydronaphthalen-1-one moieties joined together one or two CC-bonds.
DiazepanesCHEMONTID:0002920Compounds containing a diazepane rings, which is a saturated seven-membered ring with 2 nitrogen atoms and five carbon atoms.
SulfimidesCHEMONTID:0002929Organic derivatives of sulfimide, with the general formula RN=S(R=organic group).
CycloheptafuransCHEMONTID:0002936Organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.
CycloheptapyransCHEMONTID:0002937Organic heterocyclic compounds containing a cycloheptane derivative fused to a pyran. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.
DioxepinesCHEMONTID:0002939Compounds containing a dioxepane ring, which is a seven-membered aliphatic unsaturated ring with two oxygen atoms and five carbon atoms.
DioxepanesCHEMONTID:0002943Compounds containing a dioxepane ring, which is a seven-membered aliphatic saturated ring with two oxygen atoms and five carbon atoms.
DihydroisoquinolinesCHEMONTID:0002958Isoquinoline derivatives where exactly two carbon atoms joined by an aromatic bond are linked with a hydrogen atom each, resulting in a CC single bond.
Organophosphinic acids and derivativesCHEMONTID:0003014P-hydrocarbyl derivatives of phosphinic acid.
TropoloisoquinolinesCHEMONTID:0003016Organic compounds that contain a tropolone ring fused to an isoquinoline ring to form an azuleno[1,2,3-ij]isoquinoline skeleton.
IsoaporphinesCHEMONTID:0003018Alkaloids with a structure that contains the isoaporphine skeleton. Isoaporphine is an isomer of aporphine, with the difference that the N atom of the quinoline moiety is at the 1-position instead of the 6-position. This compounds also include oxoisoaporphines, which bear an oxo group at the 7-position. Oxoisoaporphines are believed to arise from aporphines via a spirodienone rearrangement.
1-azaoxoaporphinesCHEMONTID:0003019Analogues of Aporphines, where a nitrogen atom replaces the carbon atom at position 1, and a keto group at C7.
AzahomoaporphinesCHEMONTID:0003020Analogues of homoaporphines where a nitrogen atom replaces one carbon atom of the cyclopheptane ring.
OxaziridinesCHEMONTID:0003092Organic heterocyclic compounds containing oxaziridine, a three-membered ring containing an oxygen atom, a carbon atom, and a nitrogen atom.
ThiadiazinanesCHEMONTID:0003094Organic heterocyclic compounds containing a six-membered saturated heterocycle with two nitrogen, one sulfur, and three carbon atoms.
Carbothioic S-acidsCHEMONTID:0003107Organic acids with the general formula RCS-OH (R=H, organic group).
Carbothioic O-acidsCHEMONTID:0003108Organic acids with the general formula RCO-SH (R=H, organic group).
Hydroxylamine O-sulfonic acidsCHEMONTID:0003110Sulfonic acids with the general formula R-N-OS(O)(=O)=O. They can be synthesized through reaction of hydroxylamine and chlorosulfonic acids.
Hydrazinesulfinic acidsCHEMONTID:0003111Sulfinic acids with the general formula R-N-NS(=O)=O.
Sulfonohydrazonic acidsCHEMONTID:0003112Organic acids with the general formula RS(O)(=NNH2)-OH (R=H, organic group).
Sulfonimidic acidsCHEMONTID:0003113Organic acids with the general formula RS(O)(=NH)-OH (R=H, organic group).
Sulfonodihydrazonic acidsCHEMONTID:0003114Organic acids with the general formula RS(NNH2)2-OH (R=H, organic group).
Tellurinohydrazonic acidsCHEMONTID:0003115Organic acids with the general formula RTe(OH)NN (R=organyl).
Selenodiimidic acidsCHEMONTID:0003116Organic acids with the general formula R[Se](OH)(=N)=NR' (R = any atom but N).
Selenimidic acidsCHEMONTID:0003117Organic acids with the general formula R[Se](OH)NR' (R = any atom but N).
Sulfonohydrazonimidic acidsCHEMONTID:0003118Organic acids with the general formula RCO-SH (R=H, organic group).
Carbotelluroic acids and derivativesCHEMONTID:0003128Organic acids or derivatives thereof with the general formula RC(OH)=Te or RC(Te)OH (R = organyl).
Organic thioperoxidesCHEMONTID:0003135Organosulfur compounds with the general formula RSOR' (R,R' = organyl).
Aminosulfonodithioyl compoundsCHEMONTID:0003139Organosulfur compounds with the general formula RS(=S)(=S)N(R')R\" (R = organyl; R',R'' = any atom but N).
S-hydrazinosulfonimidoyl compoundsCHEMONTID:0003141Organosulfur compounds with the general formula N=S(R)(=O)N(N)R' (R=organyl, R' = any atom but N).
S-aminosulfonimidothioyl compoundsCHEMONTID:0003142Organosulfur compounds with the general formula N=S(R)(=S)N(R')R\" (R=organyl; R',R\" = any atom but N).
Sulfonohydrazonothioic o-acidsCHEMONTID:0003144Organic acids with the general formula RS(S)(=NH2)-OH (R=H, organic group).
Sulfonohydrazonothioic s-acidsCHEMONTID:0003145Organic acids with the general formula RS(O)(=NNH2)-SH (R=H, organic group).
Sulfonimidodithioic acidsCHEMONTID:0003146Organic acids with the general formula RS(S)(=NH)-SH (R=H, organic group).
Sulfonimidoselenoic acidsCHEMONTID:0003147Organic acids with the general formula SeS(R)=NR'(R=organyl, R' = any atom but N).
SulfonohydrazonamidesCHEMONTID:0003148Organic acids with the general formula RS(O)(=NNH2)-NH2 (R=H, organic group).
HydrazineselenoamidesCHEMONTID:0003149Organoselenium compounds with the general formula N(R)NC(=Se)N(R')R'' (R = organyl; R',R'' = H or organyl).
Sulfonodiimidoperoxoic acidsCHEMONTID:0003150Organic acids with the general formula RS(=NH)2-OOH (R=H, organic group).
Sulfonodiimidic acidsCHEMONTID:0003151Organic acids with the general formula RS(=NH)2-OH (R=H, organic group).
SulfonimidamidesCHEMONTID:0003154Organic compounds with the general formula RS(=O)=NR' (R = organyl, R' = any atom but N).
SulfonodiimidamidesCHEMONTID:0003155Organosulfur compounds with the general formula HN=S(R)(=NH)N(R')R\" (R = organyl; R',R\" = any atom but N).
Sulfinoimidoperoxoic acidsCHEMONTID:0003156Organic acids with the general formula RS(=N)-OOH (R=H, organic group).
ThioperoxolsCHEMONTID:0003159Organosulfur compounds with the general formula R-OSH or R-SOH (R = organyl group).
Carboperoxoic acidsCHEMONTID:0003164Organic acids with the general formula RCO-OOH (R=H, organic group).
Carboperoxoselenoic acidsCHEMONTID:0003165Organic acids with the general formula RCSe-OOH (R=H, organic group).
Carboperoxothioic OO-acidsCHEMONTID:0003166Organic acids with the general formula RCS-OOH (R=H, organic group).
Carboselenothioic S-acidsCHEMONTID:0003167Organic acids with the general formula RCSe-SH (R=H, organic group).
Carboselenothioic Se-acidsCHEMONTID:0003168Organic acids with the general formula RCS-SeH (R=H, organic group).
Carbodiselenoic acidsCHEMONTID:0003169Organic acids with the general formula RCSe-SeH (R=H, organic group).
Borinic acid derivativesCHEMONTID:0003219Compounds comprising any derivative of the boronic acid functional group, with the general structure RB(OR'')R' (R,R'=organyl; R''=H atom or Organyl group).
OrganoboroxinesCHEMONTID:0003222Organic compounds containing a boroxine ring B-substituted with an organyl group.
Sulfenyl compoundsCHEMONTID:0003260Organosulfur compounds a sulfenyl group with the general formula RS (R = organyl).
Thiosulfonic acidsCHEMONTID:0003284Organic compounds containing a thiosulfonic acid, with the general formula [H]SS(R)(=O)=O, R=organyl group.
PolypeptidesCHEMONTID:0003298Peptides containing ten or more amino acid residues.
PolystyrenesCHEMONTID:0003299Organic polymers that a made up of several consecutive units of the styrene monomer.
PolyureasCHEMONTID:0003300Organic polymers made up of 10 or more repeating urea units (R-CO(NH2)2-)n.
PolynucleotidesCHEMONTID:0003301Organic polymers made up of a sequence of at least 13 purine or pyrimidine nucleotide residues linked to one another from the 5' -end to the 3'-end through a phosphate group.
PolycarbamatesCHEMONTID:0003302Organic polymers made up of 10 or more repeating carbamate units (R-OCONH-)n.
6,6a-secoaporphinesCHEMONTID:0003332Alkaloids with a structure that contains an aminoethylphenanthrene moiety.
Organoarsonous acidsCHEMONTID:0003337As-hydrocarbyl compounds with the general formula RAs(OH)2, where R is an organic group.
ThienopyridazinesCHEMONTID:0003352Organic aromatic compounds containing a thiophene ring fused to a pyridazine ring. A thiophene is a five-member aromatic ring with one sulfur and four carbon atoms, while a pyridazine is a six-membered aromatic ring with two adjacent nitrogen atoms and four carbon atoms.
AzobenzenesCHEMONTID:0003370Organonitrogen aromatic compounds that contain a central azo group, where each nitrogen atom is conjugated to a benzene ring.
Organic dithiophosphoric acids and derivativesCHEMONTID:0003385Organic compounds that contain dithiophosphoric acid or a derivative thereof, with the general formula ROP(S)(=S)OR', (R,R'=H, or organyl group).
(2'->5')-dinucleotidesCHEMONTID:0003393Dinucleotides where the two bases are connected via a (2'->5')-phosphodiester linkage.
(3'->5')-dinucleotides and analoguesCHEMONTID:0003796Cyclic compounds consisting of two ribose moieties connected by one 5',3'-phosphodiester bond to form a cycle. Each ribose unit is N-linked to a nucleic base or an analogue thereof. Synthetic derivatives are generally more elaborated molecules in which one or the two nucleobase moieties, and/or sugar residues, and/or phosphodiester linkers have been modified.
2-arylbenzofuran flavonoidsCHEMONTID:0003405Phenylpropanoids containing the 2-phenylbenzofuran moiety.
IsobenzofuransCHEMONTID:0003408Organic aromatic compounds containing an isobenzofuran moiety.
IsocoumaransCHEMONTID:0004191Compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 1,3-dihydrofuran ring.
BenzothiopyransCHEMONTID:0003412Organic heterocyclic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.
AngucyclinesCHEMONTID:0003415Polyketides with a structure based on then benz[a]anthracene skeleton, with the particularity that the central ring of the anthracene moiety is a para-quinone.
Dihydrobenzofuran and benzofuran lignansCHEMONTID:0003418Neolignans in which the two C6-C3 units are linked together by a bond other than Cbeta-Cbeta'. They usually consist of a 1-benzofuran or 2,3-dihydro-1-benzofuran, which is substituted a the 2-, 3-, and 5-positions with a phenyl group, a methyl group, and a propyl group, respectively.
Cyclobutane lignansCHEMONTID:0003419Lignans with a structure characterized by to phenylpropanoid units coupled together through the C7-C7' and C8-C8' bonds, forming a cyclobutane ring with the C7, C7', C8', and C8 atoms.
Stemona alkaloidsCHEMONTID:0003427Alkaloids are characterized by a pyrrolo[1,2- a]azepine nucleus usually linked with two carbon chains mostly forming terminal lactone rings. Based on the different carbon chains attached to C-9 of the pyrroloazepine nucleus.
Vallesaman alkaloidsCHEMONTID:0003431Alkaloids with a structure that is based on the vallesaman skeleton, a tetracyclic compound that contains a piperidine ring fused to an indole.
S-alkyl-CoAsCHEMONTID:0003440Alkyl sulfides consisting of coenzyme A that carries an S-alkyl substituent.
(5'->5')-dinucleotidesCHEMONTID:0003468Dinucleotides where the two bases are connected via a (5'->5')-phosphodiester linkage.
AzaphilonesCHEMONTID:0003477A structurally variable family of fungal polyketide metabolites possessing a highly oxygenated pyranoquinone bicyclic core, usually known as isochromene, and a quaternary carbon center.
StilbenolignansCHEMONTID:0003495Non-conventional lignans that derived from stilbene. They are characterized by a p-dioxin ring substituted at one carbon atom by a C3C6 (phenylpropan) group and fused to one ring of the stilbene moiety.
ImidazopyrazinesCHEMONTID:0003589Organic heteropolycyclic compounds containing a pyrazine ring fused to an imidazole ring. These also include hydrogenated derivatives of the imidazopyrazine moiety. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Pyrazine is a 6-membered ring consisting of six carbon atoms and two nitrogen centers at ring positions 1 and 4.
1-azafluoranthenesCHEMONTID:0003607Organic compounds of the alkaloid family that contains a indeno[1,2,3-ij]isoquinoline nucleus.
Inorganic anionsCHEMONTID:0003611Inorganic compounds that have a negative electric charge.
Inorganic cationsCHEMONTID:0003612Inorganic compounds with a positive electric charge.
Inorganic zwitterionsCHEMONTID:0003613Inorganic neutral compounds having formal unit electrical charges of opposite sign.
GlycerophosphonolipidsCHEMONTID:0003616Lipids that contain a phosphonate group attached at a terminal carbon of a glycerol backbone.
Carbene-type 1,3-dipolar compoundsCHEMONTID:00036321,3-dipolar compounds with the general structure X:-C=Z<-> X+=C-Z- (X = C or N; Z = C, N, or O).
Molybdopterin dinucleotidesCHEMONTID:0003654A dinucleotide that is made up of a molybdopterin and a purine or pyrimidine base linked to each other through a phosphate chain.
Alkyl-CoA disulfidesCHEMONTID:0003656Compounds containing an S-alkyl group linked to the S-end of the coenzyme A moiety.
Inorganic 1,3-dipolar compoundsCHEMONTID:0003667Electrically neutral inorganic molecules carrying a positive and a negative charge in one of their major canonical descriptions. In most dipolar compounds the charges are delocalized; however the term is also applied to species where this is not the case. The term 1,3-dipolar compounds is used for those in which a significant canonical resonance form can be represented by a separation of charge over three atoms (in connection with 1,3-dipolar cycloadditions).
Pyrido[3,4-c]pyridazinesCHEMONTID:0003690Organic compounds containing a pyrido[3,4-c]pyridazine moiety. Pyrido[3,4-c]pyridazine is a 10-membered bicyclic compound made up of a pyran ring fused to a pyridazine ring so that the three nitrogen atoms are located at the 1-, 2-, and 8-position, respectively.
DiseleninsCHEMONTID:0003691Organic heterocyclic compounds containing a diselenin ring. Diselenin is a six-membered heterocyclic with for carbon atoms and two selenium atoms.
SelenanthrenesCHEMONTID:0003696Organic compounds containing a selenanthrene moiety. Selenanthrene is a tricyclic ring system that consists of two benzene rings fused to each other through a 1,4-selenine ring.
Pyrano[3,4-c]pyridazinesCHEMONTID:0003697Organic compounds containing a pyrano[3,4-c]pyridazine moiety. Pyrano[3,4-c]pyridazine is a 10-membered bicyclic compound made up of a pyran ring fused to a pyridazine ring so that the two nitrogen atoms and the oxygen atom are located at the 1-, 2-, and 8-position, respectively.
Inorganic thionylimidesCHEMONTID:0003700Inorganic compounds that contain the thionylimide group (N=S=O).
Furo[3,2-d]pyrimidine glycosidesCHEMONTID:0003707Nucleosides or derivatives thereof that consist of a furo[3,2-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They bear the sugar moiety on the pyrimidine part of the molecule.
Pyrano[3,2-d]pyrimidine glycosidesCHEMONTID:0003745Nucleosides or derivatives thereof that consist of a pyrano[3,2-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They bear the sugar moiety on the pyrimidine part of the molecule.
Furo[3,4-d]pyrimidine glycosidesCHEMONTID:0003747Nucleosides or derivatives thereof that consist of a furo[3,4-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They bear the sugar moiety on the pyrimidine part of the molecule.
Thieno[2,3-d]pyrimidine glycosidesCHEMONTID:0003748Nucleosides or derivatives thereof that consist of a thieno[2,3-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose.
v-triazolo[4,5-d]pyrimidine glycosidesCHEMONTID:0003749Nucleosides or derivatives thereof that consist of a v-triazolo[4,5-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They usually bear the sugar moiety on the pyrimidine part of the molecule. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Pyrazolo[3,4-d]pyrimidine glycosidesCHEMONTID:0003750Nucleosides or derivatives thereof that consist of a pyazolo[3,2-d]pyrimidine ring system that is N-glycosidically linked to a ribose or deoxyribose. They bear the sugar moiety on the pyrimidine part of the molecule.
Pteridine nucleosides and nucleotidesCHEMONTID:0003751Nucleosides and derivatives with a structure that consists of a pteridine that is N-linked to a ribose or deoxyribose moiety. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Akageran and related alkaloidsCHEMONTID:0003754A small group of alkaloids typified by Akagerine, a tetracyclic compound that consist of a b-carboline fused to an azepine ring, which is substituted by a methyl group and a 2-methyl butane group. Akageran and related alkaloids appears to be formed by bond-breaking of a corynanthe precursor followed by formation of a 7-membered ring.
Aspidofractine alkaloidsCHEMONTID:0003755Alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond.
Condylocarpan alkaloidsCHEMONTID:0003756Alkaloids with a structure based on the condylocarpan backbone. These alkaloids contain a ring system similar to that of the curan group, but are formed by cyclisation of C-21 on to C-7 in a Corynanthe precursor, rather than the formation of a 3,7 bond.
Ervatamia alkaloidsCHEMONTID:0003757Alkaloids with a structure based on the tetracyclic ervatamia skeleton, which arises from the 5,6- bond cleavage and 6,16- bond formation in the vobasine skeleton.
Gelsemium alkaloidsCHEMONTID:0003758Alkaloids with a structure that is based on the tetracyclic gelsemium skeleton. These alkaloids contain an oxindole function and a cage-like, hydroaromatic residue which is believed to arise from an intermediate related to anhydrovobasinediol by formation of a 6,20 bond and rearrangement to an oxindole. The major alkaloids in this group are related to Gelsemine; however, a smaller group, characterized by Gelsedine, lack the 6,20 bond, and have also lost C-21.
Macroline alkaloidsCHEMONTID:0003759Alkaloids with a structure that is based on the tetracyclic macroline skeleton. The macroline skeleton arises by scission of the C-21 to N-4 bond of the akuammilan skeleton, and mostly occurs in bisindole alkaloids.
Pandoline alkaloidsCHEMONTID:0003760Alkaloids with a structure that is based on the pentacyclic pandoline skeleton. The Pandoline (pseudoaspidospermidine) (type II indole alkaloid) nucleus is believed to be formed by cyclisation of a secodine derivative.
Melodinus alkaloidsCHEMONTID:0003761Alkaloids with a structure that is based on the melodinus skeleton. This backbone is a pentacyclic structure that contains a tetrahydroquinoline and an indolizine joined to each other through a cyclopentane.
Pleiocarpaman alkaloidsCHEMONTID:0003762Alkaloids with a structure that is based on the pleiocarpaman skeleton. These alkaloids arise from the cyclization of a corynantheine precursor via C-16 to N-1.
Schizozygine alkaloidsCHEMONTID:0003763Alkaloids with a structure based o the hexacyclic schizozygine skeleton, consisting of quinolizidine, indole, and piperidine.
Correantan alkaloidsCHEMONTID:0003764Alkaloids with a structure that is based on the correantan skeleton, which is a tetracyclic compound consisting of the seven-membered azepane ring fused to the pyridine moiety of a beta-carboline.
Kopsane alkaloidsCHEMONTID:0003765A group of compounds with a structure based on the heptacyclic kopsane skeleton, formed by attachment of C-22 (the methoxycarbonyl carbon) of Venalstonine to C-6.
Pyrrolo[3,4-d]pyridazinesCHEMONTID:0003770Organic compounds containing a pyrrolo fused to a pyridazine ring. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Pyridazine is a six-membered aromatic ring with two adjacent nitrogen atoms, and for carbon atoms.
4a-homomorphinansCHEMONTID:0003772Alkaloids with a structure based on the 4a-homomorphinan skeleton. 4a-homomorphinan is a tetracyclic compound similar to morphinan, with the difference that the benzene ring is replaced by a cycloheptatriene ring.
Androcymbine alkaloidsCHEMONTID:0003773Alkaloids with a structure that is based on the androcymbine skeleton. This is a tetracyclic compound analogous to dibenzocycloheptane, where one benzene ring carries a ketone.
4,5-epoxy-10-normorphinansCHEMONTID:0003774Alkaloids with a structure based on the 4,5-epoxy-10-normorphinan skeleton. These compounds possess a morphinan skeleton that lacks B-ring.
Phenethylisoquinoline alkaloidsCHEMONTID:0003775Alkaloids with a structure based on the phenethylisoquinoline skeleton. Phenethylisoquinoline is a tricyclic compound that consists of a quinoline that is carries a phenethyl group at the 2-position.
Allocolchicine alkaloidsCHEMONTID:0003776Alkaloids with a structure based on the tricyclic allocolchicine skeleton, which consists of a dibenzocycloheptane where the cycloheptane moiety carries the N-acetamide group.
Lumicolchicine alkaloidsCHEMONTID:0003777Alkaloids with a structure based on the tetracyclic lumicolchicine skeleton. They can derive from a colchicine precursor where the cycloheptatriene ring is replaced with a bicyclo[3.2.0]hepta-2,6-diene ring system.
Cephalotaxus alkaloidsCHEMONTID:0003778Alkaloids with a structure based on the cephalotaxine skeleton, a tetracyclic 1,3-benzodioxole-containing compound which arises from the skeletal rearrangement of the hydroaromatic component of the Erythrina group.
QuinolidinesCHEMONTID:0003787Organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring.
Strictosidine alkaloidsCHEMONTID:0003791Alkaloids with a structure that is based on the strictosidine skeleton, which contains the tricyclic beta-carboline moiety.
Phosphorothioate polynucleotidesCHEMONTID:0003799Polynucleotides in which one of the non-bridging oxygens in each phosphodiester linkage has been replaced by sulfur.
Indolonaphthyridine alkaloidsCHEMONTID:0003805A numerous and relatively straightforward subgroup of the b-carbolines, e.g. Canthin-6-one, in which an additional C3 unit is attached between C-1 and the indole nitrogen to form an additional ring. The group includes a few dimeric examples, such as Haplophytine.
Carbothioic S-estersCHEMONTID:0003872Ester derivatives of carbothioic S-acids, with the general structure RSC(=O)R' where R = organyl group and R' = H or organyl group.
Carbothioic S-lactonesCHEMONTID:0003873Cyclic organosulfur compounds with the general structure RC(=O)SR', R-R' = organyl group, where the central atom is part of the ring.
Carbothioic O-estersCHEMONTID:0003874Ester derivatives of carbothioic O-acids, with the general structure ROC(=S)R' where R = organyl group and R' = H or organyl group.
Carbothioic O-lactonesCHEMONTID:0003875Cyclic organosulfur compounds with the general structure RC(=S)OR', R-R' = organyl group, where the central atom is part of the ring.
Carbothioic halidesCHEMONTID:0003876Organosulfur compounds with the general structure RC(=S)X, where R = organyl group and X = halogen atom.
Carbodithioic acid estersCHEMONTID:0003877Ester derivatives of a carbodithioic acid (RC(=S)SH).
CarbodithiolactonesCHEMONTID:0003878Cyclic organosulfur compounds with the general formula RC(=S)SR', where the central carbon atom is part of a ring; R,R' = organyl group.
ImidolactamsCHEMONTID:0003886Cyclic organooxygen compounds containing the structure RC(=N)N where the central carbon atom and one of the linked nitrogen atoms are part of the same ring( R here is an organyl group). They can also be viewed as analogs of lactams where the oxygen atom is replaced by a nitrogen atom.
Vinylogous acidsCHEMONTID:0003889Organic compounds containing a hydroxyl group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety.
Vinylogous amidesCHEMONTID:0003890Organic compounds containing an amine group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety.
Vinylogous estersCHEMONTID:0003891Organic compounds containing an ester group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety.
HaloalkenesCHEMONTID:0003903Compounds derived from an alkene by replacing a hydrogen atom with a halogen atom.
HydrobromidesCHEMONTID:0003920Organic salts that results from the reaction of hydrobromic acid with an organic base.
HydrochloridesCHEMONTID:0003921Organic salts that results from the reaction of hydrochloric acid with an organic base.
Organic sulfate saltsCHEMONTID:0003929Organic compounds containing a sulfate ion.
Organic bromide saltsCHEMONTID:0003930Organic compounds containing a bromine ion.
Organic chloride saltsCHEMONTID:0003931Organic compounds containing a chlorine ion.
Organic iodide saltsCHEMONTID:0003932Organic compounds containing a iodine ion.
Organic perchlorate saltsCHEMONTID:0003933Organic compounds containing a perchlorate ion.
Dithiocarbamic acids and derivativesCHEMONTID:0003934Organosulfur compounds with the general formula SC(=S)N(R1)R2; R1-R2 = H or organyl group.
Phosphine imidesCHEMONTID:0003939Organophosphorus compounds with the general formula R1P(R2)(R3)N=R4; R1 = organyl, R2-R4 = H or organyl.
Inorganic arsenic compoundsCHEMONTID:0004057Inorganic compounds containing the arsenic atom.
Inorganic sulfidesCHEMONTID:0003942Inorganic compounds of sulfur with a less electronegative element.
Inorganic phosphidesCHEMONTID:0003943Inorganic compounds containing phosphorus with a less electronegative element or elements.
Inorganic oxidesCHEMONTID:0003944Inorganic chemical compounds with one or more oxygen atoms combined with another element.
Inorganic hydridesCHEMONTID:0003945Inorganic compounds in which hydrogen is bonded to a more electropositive element or group. Usually, they contain one or more hydrogen centers having nucleophilic, reducing, or basic properties.
Inorganic selenidesCHEMONTID:0003946Inorganic chemical compounds in which selenium serves as an anion with oxidation number of -2. The selenium atom here when participating in a chemical bond, is linked to a less electronegative atom.
Inorganic nitrosaminesCHEMONTID:0003948Inorganic compounds containing the nitrosamine functional group, with the structure R2NN=O.
Inorganic hydroxylaminesCHEMONTID:0003949Inorganic compounds containing the hydroxylamine group RN(R')-OH, where R,R' = H or inorganic moiety.
Isporenylated bicyclo [2.2.2] alkaloidsCHEMONTID:0003950Alkaloids characterized by the unique bicyclo [2.2.2] ring system, constituted mainly from tryptophan, proline, or substituted proline derivatives, where the olefinic unit of the isoprene moiety is usually oxidatively cyclized across the alpha carbon of a cyclic dipeptide (a piperazinedione).
DiarsolanesCHEMONTID:0003985Organic compounds containing a diarsolane ring, which is a saturated five-membered ring made up of three carbon and two arsenic atoms.
SulfonediimidesCHEMONTID:0003991Compounds having the structure, RS(=NR)2R', formally derived from sulfones by replacing (=O)2 by (=NR)2. R = organyl group, R' = H or organyl group.
Inorganic cobalt saltsCHEMONTID:0003996Inorganic salts containing a cobalt ion.
Organic metal saltsCHEMONTID:0004036Organic salt compounds containing a metal atom in its ionic form.
Inorganic copper saltsCHEMONTID:0004019Inorganic salts containing a copper ion.
Vinylogous thioestersCHEMONTID:0004020Organic compounds containing a thioester group, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety.
Cyanide saltsCHEMONTID:0004026Organic compounds containing the cyanide anion [C-]#N.
Inorganic tin saltsCHEMONTID:0004039Inorganic salt compounds containing a tin atom either in its ionic form or bonded to another atom.
Inorganic lead saltsCHEMONTID:0004052Inorganic salts containing a lead ion.
Inorganic mercury compoundsCHEMONTID:0004060Inorganic compounds containing a mercury atom.
Inorganic nickel compoundsCHEMONTID:0004061Inorganic compounds containing a nickel atom.
Inorganic silver saltsCHEMONTID:0004062Inorganic salts containing a silver ion or a bonded silver atom.
Inorganic chromium (VI) compoundsCHEMONTID:0004074Inorganic compounds containing one or more hexavalent chromium atoms.
Inorganic cadmium saltsCHEMONTID:0004076Inorganic salts of cadmium. They usually contain cadmium in its ionic form.
Inorganic antimony saltsCHEMONTID:0004077Inorganic salts of antimony. They usually contain antimony in its ionic form.
ThiodisulfinatesCHEMONTID:0004086Organosulfur compounds with the general formula RS(=O)S, where R = organyl group.
Inorganic sodium saltsCHEMONTID:0004102Inorganic salt compounds containing a sodium atom either in its ionic form or bonded to another atom (metal or halogen).
Inorganic chloride saltsCHEMONTID:0004103Inorganic salt compounds containing a chlorine atom either in its ionic form or bonded to another atom (metal or halogen).
1,3,5-triazine ribonucleosides and ribonucleotidesCHEMONTID:0004104Nucleosides or nucleotides with a structure that consists of a 1,3,5-triazine ring, which is N-linked to a ribose (or deoxyribose). Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
6,7-benzomorphansCHEMONTID:0004131Opioid alkaloids based on the tricyclic 6,7-benzomorphan skeleton. Benzomorphans are derived from morpholine, but lack its C ring.
Thiohydroximic acids and derivativesCHEMONTID:0004136Organosulfur compounds containing the thiohydroximic acid group (RC(S)=NOH, where R = H or organyl group) or a derivative thereof.
Azacyclic compoundsCHEMONTID:0004139Organic compounds containing an heterocycle with at least one nitrogen atom and one carbon atom linked to each other.
Oxacyclic compoundsCHEMONTID:0004140Organic compounds containing an heterocycle with at least one oxygen atom linked to a ring carbon.
Phosphacyclic compoundsCHEMONTID:0004141Organic compounds containing an heterocycle with at least one phosphorus atom and one carbon atom linked to each other.
Heteroaromatic compoundsCHEMONTID:0004144Compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
Polycyclic hydrocarbonsCHEMONTID:0004149Polycyclic organic compounds made up only of carbon and hydrogen atoms.
ThioselenidesCHEMONTID:0004163Organic compounds containing a sulfur-selenium bond. This class is restricted to compounds where at least one of the sulfur or selenium atoms is linked to a carbon atom.
PhenoselenazinesCHEMONTID:0004166Organic compounds containing two benzene rings joined together by a selenomorpholine ring.
SelenophenesCHEMONTID:0004169Organic compounds containing selenophene, a five-membered monocyclic aromatic ring composed of four C atoms and one selenium atom.
OxirenesCHEMONTID:0004170Organic compounds containing oxirene, an unsaturated three-membered ring with two carbon atoms and one oxygen atom.
Pyridine nucleosidesCHEMONTID:0004174Compounds comprising a pyridine base attached to a ribosyl or deoxyribosyl moiety.
TrialkylphosphanesCHEMONTID:0004186Organophosphorus compounds with the general formula R3P=O.
CoumaransCHEMONTID:0004189Compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring.
ThienothiophenesCHEMONTID:0004193Organic compounds containing two thiophene rings fused to each other.
Allyl sulfur compoundsCHEMONTID:0004195Compounds containing an allylsulfur group, with the general structure H2C(=CH2)CS.
5'-O-tritylated nucleosides and derivativesCHEMONTID:0004232Ribonucleosides or derivatives, in which the ribose moiety carries a trityl group at the 5' position, and is N-linked at the to either a purine or a pyrimidine base.
6-ThiathiophenesCHEMONTID:0004236Aromatic heterocyclic compounds containing a 6-thiathiophene ring system, an analog of thieno[2,3-b]thiophene, with three adjacent sulfur atoms.
Arsonous acid estersCHEMONTID:0004246Organoarsonous acid derivatives, where the two oxygen atoms are esterified.
Organoarsinous acid estersCHEMONTID:0004247Organoarsonous acid derivatives, where the hydrogen atom of the hydroxyl group is replaced by an organyl group.
Organoarsinous acidsCHEMONTID:0004248As-hydrocarbyl compounds with the general formula R2As(OH), where R is an organic group.
Daphniphylline-type alkaloidsCHEMONTID:0004324Alkaloids (or derivatives thereof) from the genus Daphniphyllum, possessing 22 carbon polycyclic fused ring systems with or without the C8 side chain. The C8 unit consists of 6-oxabicyclo[3.2.1]octane or 2,8-dioxabicyclo[3.2.1]octane.
Yuzurimine-type alkaloidsCHEMONTID:0004326Alkaloids (or derivatives thereof) from the genus Daphniphyllum that contain a 22 carbon core, commonly with a C9-C10 double bond, and C-22 is mostly a methyl ester of a carboxyl group.
Tetraalkylphosphonium compoundsCHEMONTID:0004327Organophosphorus compounds that contain a tetravalent phosphorus atom substituted to four alkyl chains.
Tetraalkylphosphonium halidesCHEMONTID:0004328Organophosphorus compounds that contain an halogen atom, and a tetravalent phosphorus atom substituted to four alkyl chains.
Indeno[1,2-c]pyrazolesCHEMONTID:0004345Aromatic heterocyclic compounds that contain indeno[1,2-c]pyrazole, which consists of a pyrazole ring fused to an indene ring system.
Deoxyribo- and ribonucleoside phosphonatesCHEMONTID:0004350N-glycosyl compound that possess both a nucleobase, usually a purine or a pyrimidine, linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.
Imidazole[4,5-c]pyridine ribonucleosides and ribonucleotidesCHEMONTID:0004353Organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole[4,5-c]pyridine ring system. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.
Sulfonothioic O-acidsCHEMONTID:0004357Organosulfur compounds with the general formula RS(O)(S)-OH.
Pyrazolo[3,4-b]pyrazinesCHEMONTID:0004370Aromatic heterocyclic compounds containing a pyrazole ring and a pyrazine ring fused to one another without sharing a nitrogen atom.
Pyrazolo[1,5-b]pyridazinesCHEMONTID:0004371Aromatic heterocyclic compounds containing a pyrazole ring fused to and sharing a nitrogen atom with a pyridazine ring.
Pyrazolo[1,5-a][1,3,5]triazinesCHEMONTID:0004372Aromatic heterocyclic compounds containing a pyrazole ring fused to and sharing a nitrogen atom with a 1,3,5-triazine ring.
Pyrazolo[1,5-d][1,2,4]triazinesCHEMONTID:0004373Aromatic heterocyclic compounds containing a pyrazole ring fused to and sharing a nitrogen atom with a 1,2,4-triazine ring.
Pyrazolo[4,3-e]pyrrolo[1,2-a]pyrazinesCHEMONTID:0004375Aromatic heterocyclic compounds containing pyrrole fused and shares one nitrogen atom with the pyrazine moiety of a pyrazolo[3,4-a]pyrazine ring system.
Imidazo[1,2-a]pyrazin-8-onesCHEMONTID:0004376Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a pyrazine ring. The bicyclic moiety carries an oxo group at the 8-position.
Imidazo[1,2-a]pyrimidinesCHEMONTID:0004377Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a pyrimidine ring.
Imidazo[1,2-a][1,2,4]triazinesCHEMONTID:0004378Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a 1,2,4-triazine ring. In imidazo[1,2-a][1,2,4]triazines the 1,2,4-triazine ring shares the atom at the 2-position with the imidazole ring.
Imidazo[1,2-d][1,2,4]triazinesCHEMONTID:0004379Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a 1,2,4-triazine ring. In imidazo[1,2-d][1,2,4]triazines the 1,2,4-triazine ring shares the atom at the 4-position with the imidazole ring.
Imidazo[2,1-c][1,2,4]triazinesCHEMONTID:0004380Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a 1,2,4-triazine ring.
Imidazo[4,3-c][1,2,4]triazinesCHEMONTID:0004381Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a 1,2,4-triazine ring.
Pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazinesCHEMONTID:0004382Aromatic heterocyclic compounds containing a pyrimidine fused to both a pyrazole and a pyridazine rings. In this ring system, pyrimidine shares one atom with the pyrazole ring, and no nitrogen atom with the pyrazole ring.
Imidazo[1,5-a]pyrazinesCHEMONTID:0004388Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a pyrazine ring.
Imidazo[1,2-a]pyridinesCHEMONTID:0004396Aromatic heteropolycyclic compounds containing an imidazole ring fused to and sharing one nitrogen with a pyridine ring.
1,3-thiazolo[5,4-d]pyrimidinesCHEMONTID:0004401Aromatic heteropolycyclic compounds containing a 1,3-thiazolo[5,4-d]pyrimidine ring system, which consists of a 1,3-thiazole ring fused to but not sharing a nitrogen atom with a pyrimidine ring.
Ribonucleoside 3'-phosphatesCHEMONTID:0004404Ribonucleosides that contain a phosphate group attached to the C-3 carbon of the ribose or deoxyribose moiety. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
PyridopyrazinesCHEMONTID:0004405Aromatic heteropolycyclic compounds containing a pyridine ring fused to a pyrazine ring.
FuropyridinesCHEMONTID:0004407Aromatic heterocyclic compounds containing a furopyridine ring system, which consists of a furan ring fused to a pyridine ring.
Furo[2,3-d]pyrimidinesCHEMONTID:0004416Aromatic heteropolycyclic compounds containing a furo[2,3-d]pyrimidine ring system, which is a furopyrimidine isomer having the on ring oxygen atom, and 2 nitrogen atoms at the 1-, 5-, and 7-positions, respectively.
Inorganic silicidesCHEMONTID:0004432Inorganic compounds containing silicon with a less electronegative element or elements (according to the Pauling scale).
Borate estersCHEMONTID:0004433Ester derivatives of boric acid, with the generic formula ROB(OR')OR\", where R is an organic group.
Metal alkylsCHEMONTID:0004436Organometallic compounds hat containing a metal atom substituted by on or more alkyl groups.
Metal arylsCHEMONTID:0004440Organometallic compounds hat containing a metal atom substituted by on or more aryl groups.
Metal allylsCHEMONTID:0004441Organometallic compounds containing an allylic group attached to the metal atom.
Metal alkyl halidesCHEMONTID:0004442Organometallic compounds with the generic formula R-M-X, where R is an alkyl group, and X is a metal atom.
Organic sulfite saltsCHEMONTID:0004455Organic salts of the sulfite ion.
Organic thiosulfate saltsCHEMONTID:0004457Organic salts of the thiosulfate ion.
Organic bromate saltsCHEMONTID:0004458Organic salts of bromate. They contain bromate in its ionic form or conjugated to a metal atom.
Organic selenite saltsCHEMONTID:0004459Organic salts containing a selenite group, in its ionic form or bound to a metal atom.
Organic iodate saltsCHEMONTID:0004460Organic salts containing the iodate group, in its ionic form or bound to a metal atom.
Organic chlorite saltsCHEMONTID:0004462Organic salts containing the chlorite group, in its ionic form or bound to a metal atom.
Organic phosphite saltsCHEMONTID:0004463Organic salts containing a phosphite group, in its ionic form or bound to a metal atom.
Inorganic azidesCHEMONTID:0004464Inorganic compounds bearing the group N3, viz. -N=N+=N-.
Salt-like carbidesCHEMONTID:0004468Inorganic salts containing a carbon atom combined with one or more elements of similar or lower electronegativity.
Inorganic nitridesCHEMONTID:0004470Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3.
Inorganic nitritesCHEMONTID:0004471Inorganic compounds containing the nitrite ion NO2-.
Aromatic hydrocarbonsCHEMONTID:0004477Aromatic compounds that are made up of carbon and hydrogen atoms only.
AcetylidesCHEMONTID:0004478Compounds arising by replacement of one or both hydrogen atoms of acetylene (ethyne) by a metal or other cationic group. E.g. NaC#CH monosodium acetylide. By extension, analogous compounds derived from terminal acetylenes, RC#CH. The class is limited here to derivatives of acetylene where the hydrogen atom is replaced with an element with similar or lower electronegativity that carbon.
Alkylphosphonofluoridic acids and estersCHEMONTID:0004483Organophosphorus compounds containing a phosphonic acid or an ester derivative thereof, where the phosphorus atom is directly attached to an alkyl group.
TrialkylphosphitesCHEMONTID:0004484Organic compounds containing a phosphorous acid, which is tri-esterified with alkyl groups.
Inorganic lithium saltsCHEMONTID:0004487Inorganic salts containing a lithium ion.
Inorganic beryllium saltsCHEMONTID:0004490Inorganic salts of cadmium. They usually contain beryllium in its ionic form.
Inorganic calcium saltsCHEMONTID:0004494Inorganic salts containing a calcium ion.
2',3'-dideoxy-3'-thionucleosidesCHEMONTID:00044982',3'-deoxyribonucleosides, where the ribose unit is thio-substituted at the 3'-position. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
2',3'-dideoxy-3'-thionucleoside triphosphatesCHEMONTID:00044992',3'-deoxyribonucleoside derivatives, where the ribose unit is thio-substituted at the 3'-position, and at the 5'-position by a triphosphate group. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
2',3'-dideoxy-3'-thionucleoside diphosphatesCHEMONTID:00045002',3'-deoxyribonucleoside derivatives, where the ribose unit is thio-substituted at the 3'-position, and at the 5'-position by a diphosphate group. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
2',3'-dideoxy-3'-thionucleoside monophosphatesCHEMONTID:00045012',3'-deoxyribonucleoside derivatives, where the ribose unit is thio-substituted at the 3'-position, and at the 5'-position by a monophosphate group. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
5'-deoxyribonucleosidesCHEMONTID:0004502Nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
PhosphiranesCHEMONTID:0004507Heterocyclic compounds containing a phosphirane, which is a three-membered saturated ring made up of two carbon atoms and phosphorus atoms.
Triphenyl compoundsCHEMONTID:0004524Aromatic compounds containing a triphenyl moiety.
Inorganic thalium compoundsCHEMONTID:0004540Inorganic molecular entities containing one or more thalium atoms.
Inorganic pnictogen compoundsCHEMONTID:0004558Compounds containing one or more pnictogen atoms. Pnictogens are p-block element atoms that are in the group 15 of the periodic table.
Inorganic 3-nitrosotriazenesCHEMONTID:0004563Inorganic compounds containing a 3-nitrosotriazene moiety, with the formula N=N-N-N=O.
Haloacetylenes and derivativesCHEMONTID:0004565Organohalogen compounds containing an acetylene group substituted with one or more halogen atoms.
AlkylhalophosphinesCHEMONTID:0004572Organophosphorus compounds with the general formula RPX2 or R2PX (R=alkyl, X=halogen).
Organometallic peroxidesCHEMONTID:0004614Organic compounds that contain a peroxide group substituted with a an organometallic group.
1-hydroxylamino, 2-unsubstituted benzenoidsCHEMONTID:0004648Benzenoids in which the benzene moiety is N-linked to an hydroxylamine at the 1-position, and unsubstituted at the 2-position.
1-hydroxylamino, 4-unsubstituted benzenoidsCHEMONTID:0004649Benzenoids in which the benzene moiety is N-linked to an hydroxylamine at the 1-position, and unsubstituted at the 4-position.
N-phenylhydroxylaminesCHEMONTID:0004650Hydroxylamines that are N-substituted with a phenyl group.
O-phenylhydroxylaminesCHEMONTID:0004651Hydroxylamines that are O-substituted with a phenyl group.
Benzo-1,2,3-triazinesCHEMONTID:0004659Organic compounds containing a 1,2,3-triazine ring fused to a benzene ring.
Organic thiosulfinic acidsCHEMONTID:0004703Organic compounds containing a thiosulfinyl group (HS(S)OH). They have the general structure RS(=S)OH, where R = H or organyl.
OxadiazinesCHEMONTID:0004736Heterocyclic compounds containing an oxadiazine ring, which is an unsaturated six-membered heterocycle that consists of one oxygen 2 nitrogen, and 3 carbon atoms.
2',5'-dideoxyribonucleosidesCHEMONTID:0004799Nucleosides characterized by a purine or pyrimidine base, which is N-linked to a 2',5'-dideoxyribose moiety.
AcenaphthylenesCHEMONTID:0004812Aromatic polycyclic compounds containing an acenaphthylene moiety. Acenaphthylene is a carbotricyclic compound, consisting of a naphthalene with positions C1 and C8 connected by an ethylene bridge.
Inorganic chromium trioxidesCHEMONTID:0004819Inorganic compounds containing a chromium trioxide moiety.
Selenenic acidsCHEMONTID:0004826Aromatic compounds containing a moiety of the generic structure RSeOH, where R is an organic group.
PyrroloquinolinesCHEMONTID:0001734Compounds containing a pyrroloquinoline moiety, which consists of a pyrrole ring fused to a quinoline.
AmidinesCHEMONTID:0000007Derivatives of oxoacids RnE(=O)OH in which the hydroxy group is replaced by an amino group and the oxo group is replaced by =NR. Amidines include carboxamidines, sulfinamidines and phosphinamidines.
DiterpenoidsCHEMONTID:0001551Terpene compounds formed by four isoprene units.
SulfinesCHEMONTID:0000009S-Oxides of thioaldehydes and thioketones.
SulfenesCHEMONTID:0000010S,S-Dioxides of thioaldehydes and thioketones, R2C=SO2.
Carbohydrates and carbohydrate conjugatesCHEMONTID:0000011Monosaccharides, disaccharides, oligosaccharides, polysaccharides, and their derivatives.
Amino acids, peptides, and analoguesCHEMONTID:0000013Organic compounds containing an amino acid or a peptide backbone, or derivatives thereof.
PhenylbutylaminesCHEMONTID:0000014Compounds containing a phenylbutylamine moiety, which consists of a phenyl group substituted at the fourth carbon by an butan-1-amine.
DibenzofuransCHEMONTID:0000015Compounds containing a dibenzofuran moiety, which consists of two benzene rings fused to a central furan ring.
Purine ribonucleotidesCHEMONTID:0001544Nucleotides consisting of a purine base linked to a ribose to which at least one phosphate group is attached.
Pyridine carboxaldehydesCHEMONTID:0002212Aromatic compounds containing a pyridine ring which bears a carboxaldehyde group.
EicosanoidsCHEMONTID:0000513Unsaturated C20 fatty acids or skeletally related compounds. These include prostaglandins, thromboxanes, leukotrienes and other oxygenated derivatives, which are produced primarily by three classes of enzymes, cyclooxygenases (COX-1 and COX-2), lipoxygenases (LOX) and cytochrome P450 mono-oxygenases.
BenzenesulfonamidesCHEMONTID:0000031Organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
Benzenesulfonic acids and derivativesCHEMONTID:0000032Organic compounds containing a sulfonic acid or a derivative thereof that is linked to a benzene ring.
Benzyl alcoholsCHEMONTID:0000033Organic compounds containing the phenylmethanol substructure.
HalobenzenesCHEMONTID:0000035Aromatic compounds containing a halogen atom linked to a benzene ring.
NitrobenzenesCHEMONTID:0000036Compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
StyrenesCHEMONTID:0000037Organic compounds containing an ethenylbenzene moiety.
SulfanilidesCHEMONTID:0000038Organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.
IndanonesCHEMONTID:0001151Compounds containing an indane ring bearing a ketone group.
Biphenyls and derivativesCHEMONTID:0000041Organic compounds containing to benzene rings linked together by a C-C bond.
DiphenhydraminesCHEMONTID:0000042Cyclic aromatic compounds containing a diphenhydramine moiety, which consists of a diphenylmethoxyl group like to an ethyldimethylamine to form [2-(diphenylmethoxy)ethyl]dimethylamine.
PhenylbenzimidazolesCHEMONTID:0000330Compounds containing a phenylbenzimidazole skeleton, which consists of a benzimidazole moiety where its imidazole ring is attached to a phenyl group.
PhenylpropenesCHEMONTID:0000045Compounds containing a phenylpropene moiety, which consists of a propene substituent bound to a phenyl group.
PodophyllotoxinsCHEMONTID:0000047Tetralin lignans in which the benzene moiety of the tetralin skeleton is fused to a 1,3-dioxolane and the cyclohexane is fused to a butyrolactone (pyrrolidin-2-one).
TametralinesCHEMONTID:0000049Compounds containing a tametraline moiety, which consists of a tetrahydronaphthalene linked to a phenyl group to form N-methyl-4-phenyl-1,2,3,4-tetrahydronaphthalen-1-amine skeleton.
MonoterpenoidsCHEMONTID:0001549Compounds containing a chain of two isoprene units.
Aminoquinolines and derivativesCHEMONTID:0000053Organic compounds containing an amino group attached to a quinoline ring system.
BenzylisoquinolinesCHEMONTID:0000054Organic compounds containing an isoquinoline to which a benzyl group is attached.
DibenzothiazepinesCHEMONTID:0000055Compounds containing a dibenzothiazepine moiety, which consists of two benzene connected by a thiazepine ring.
Quinolones and derivativesCHEMONTID:0000056Compounds containing a quinoline moiety which bears a ketone group.
HydroxyquinolinesCHEMONTID:0000057Compounds containing a quinoline moiety bearing a hydroxyl group.
Hydroxycinnamic acids and derivativesCHEMONTID:0001391Compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated.
IndoloquinolinesCHEMONTID:0000061Polycyclic aromatic compounds containing an indole fused to a quinoline.
Nitrate estersCHEMONTID:0000063Compounds containing a nitrate ester functional group, with the general structure RON+(=O)O, (R cannot be a hydrogen).
ArsolesCHEMONTID:0000065Organic compounds containing an arsacyclopentadiene ring (a five member ring with one arsenic atom, four carbon atoms, and two double bonds).
PyrazinesCHEMONTID:0000067Compounds containing a pyrazine ring, which is a six-member aromatic heterocycle, that consists of two nitrogen atoms (at positions 1 and 4) and four carbon atoms.
DibenzodiazepinesCHEMONTID:0000072Compounds containing a dibenzodiazepine moiety, which consists of two benzene connected by diazepine ring.
Pyridazines and derivativesCHEMONTID:0000074Compounds containing a pyridazine ring, which is a six-member aromatic ring containing two nitrogen atoms at positions 1 and 2, and four carbon atoms.
Pyrimidines and pyrimidine derivativesCHEMONTID:0000075Compounds containing a pyrimidne ring, which is a six-member aromatic heterocycle which consists of two nitrogen atoms (at positions 1 and 3) and four carbon atoms.
ImidazolesCHEMONTID:0000078Compounds containing an imidazole ring, which is an aromatic five-member ring with two nitrogen atoms at positions 1 and 3, and three carbon atoms.
ImidazolinesCHEMONTID:0000079Organic compounds containing an imidazoline ring, which is an unsaturated ring (derived from imidazole) with two nitrogen atoms at positions 1 and 3 respectively, and containing only one CN double bond.
IndazolesCHEMONTID:0000080Compounds containing an indazole, which is structurally characterized by a pyrazole fused to a benzene.
IsoxazolesCHEMONTID:0000081Heterocyclic organic compounds containing an isoxazole moiety, with a structure characterized by a five-member aromatic ring with one oxygen atom and one nitrogen atom at ring positions 1 and 2, respectively.
OxazolesCHEMONTID:0000083Compounds containing an oxazole ring, which is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole.
OxazolinesCHEMONTID:0000084Organic compounds containing 1,3-oxazoline, a five-membered ring with a nitrogen and an oxygen atoms at the 1- and 3-position, respectively. Additionally, it contains two double bonds.
PhosphininesCHEMONTID:0000085Compounds containing a phosphinine ring, which is a benzene derivative where a carbon ring is replaced by a phosphorus atom.
PyrazolesCHEMONTID:0000087Compounds containing a pyrazole ring, which is a five-member aromatic ring with two nitrogen atoms (at positions 1 and 2) and three carbon atoms.
PyrazolinesCHEMONTID:0000088Compounds containing a pyrazoline ring, which is a five-member saturated aliphatic ring with two nitrogen atoms (at positions 1 and 2) and three carbon atoms.
ThiadiazolesCHEMONTID:0000093Cyclic organic compounds containing a thiadiazole ring, which is a five-membered aromatic heterocycle made up of one sulfur atom and two nitrogen atoms.
ThiazolesCHEMONTID:0000095Heterocyclic compounds containing a five-member aromatic ring made up of one sulfur atom, one nitrogen, and three carbon atoms.
TriazolesCHEMONTID:0000099Compounds containing a five-member aromatic ring of two carbon atoms and three nitrogen atoms.
BenzoquinolinesCHEMONTID:0001908Organic compounds containing a benzene fused to a quinoline ring system.
SesquiterpenoidsCHEMONTID:0001550Terpenes with three consecutive isoprene units.
OxazolidinesCHEMONTID:0000108Compounds containing an oxazolidine moiety, which consists of a saturated aliphatic five-member ring with one oxygen atom, one nitrogen, three carbon atoms, and two double bonds.
Pterins and derivativesCHEMONTID:0000110Polycyclic aromatic compounds containing a pterin moiety, which consist of a pteridine ring bearing a ketone and an amine group to form 2-aminopteridin-4(3H)-one.
TetrazolesCHEMONTID:0000111Organic compounds containing a tetrazole ring, which is a five-member aromatic heterocycle made up of four nitrogen atoms and a one carbon atom.
Hydrazines and derivativesCHEMONTID:0000112Compounds comprising the hydrazine functional group, with the general formula R1R2NNR3R4.
PhenylhydrazinesCHEMONTID:0000113Compounds containing a phenylhydrazide moiety, which consists of a hydrazide substituent attached to a phenyl group.
IminesCHEMONTID:0000117Compounds containing an imine functional group, with the general structure RN=CR2 (R = H, hydrocarbyl).
Carbonyl compoundsCHEMONTID:0001831Organic compounds containing a carbonyl group, with the general structure RC(=O)R', where R=organyl, R'=H, N, O, organyl group or halide group.
AcetophenonesCHEMONTID:0000119Organic compounds containing the acetophenone structure.
BenzophenonesCHEMONTID:0000120Organic compounds containing a ketone attached to two phenyl groups.
ThioketonesCHEMONTID:0000121Compounds in which the oxygen of a ketone has been replaced by divalent sulfur R2C=S ( R not H ). Thioketones that have an alpha-hydrogen interconvert with Thioenols. Moreover, they interconvert with thioaldehydes.
IsoindolesCHEMONTID:0000127Heteropolycyclic compounds with a structure containing isoindole, a benzo-fused pyrrole.
EthersCHEMONTID:0000254Compounds bearing an ether group with the formula Compounds ROR (R not H).
Alcohols and polyolsCHEMONTID:0000129Organic compounds in which at least one hydroxyl functional group (-OH) is bound to a carbon atom, usually connected to other carbon or hydrogen atoms.
EnediolsCHEMONTID:0000131Compounds containing the enediol functional group, with the formula HO(R)C=C(R')OH.
EnolsCHEMONTID:0000132Compounds containing the enol functional group, with the structure HO(R)C=CR'. Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.
BenzenediolsCHEMONTID:0001286Organic compounds containing two hydroxyl groups attached to a benzene ring.
AnisolesCHEMONTID:0000138Organic compounds containing a methoxybenzene or a derivative thereof.
Tyrosols and derivativesCHEMONTID:0000139Compounds containing a hydroxyethyl group attached to the C4 carbon of a phenol group.
AminophenolsCHEMONTID:0000140Organic compounds containing an amino group attached to a phenol.
NitrophenolsCHEMONTID:0000141Compounds containing a nitrophenol moiety, which consists of a benzene ring bearing both a hydroxyl group and a nitro group on two different ring carbon atoms.
Stilbene glycosidesCHEMONTID:0000142Compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.
DiphenylmethanesCHEMONTID:0000369Compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.
1-benzopyransCHEMONTID:0003410Organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position.
DithiazolesCHEMONTID:0000148Compounds containing a dithiazole moiety, which consists of an unsaturated five-member ring containing two carbon atoms, one nitrogen atom, and two sulfur atoms.
DibenzoxazepinesCHEMONTID:0000150Compounds containing a dibenzoxazepine moiety, which consists of two benzene connected by an oxazepine ring.
AnthraquinonesCHEMONTID:0000151Organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.
NaphthoquinonesCHEMONTID:0000153Compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone).
TetracenequinonesCHEMONTID:0000155Polyaromatic hydrocarbon derivatives containing a tetracyclic cycle made up of four linearly fused benzene rings, one of which bears two ketone groups at position 1 and 4.
CarbodiimidesCHEMONTID:0000157Organic compounds containing a functional group consisting of the formula RN=C=NR.
N-organohydroxylaminesCHEMONTID:0000158Organic compounds comprising the hydroxylamine functional group, with the general structure R1ON(R2)R3 (R1,R3=H, organyl; R2 = organyl).
Epothilones and analoguesCHEMONTID:0000161Macrolides consisting of a 16-member lactone ring conjugated at the carbon 16 with a 1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl group. Some epothilone analogues containing a lactam ring instead of the lactone ring.
Beta lactamsCHEMONTID:0000162Organic compounds containing a four-member lactam (a cyclic amide).
CaprolactamsCHEMONTID:0000163Cyclic amides of caproic acid. Caproic acid is the carboxylic acid derived from hexane with the general formula C5H11COOH.
Delta lactamsCHEMONTID:0000164Cyclic organic compounds containing a piperidin-2-one moiety.
Gamma lactamsCHEMONTID:0000165Organic compounds containing a gamma-lactam moiety, which consists of a five-member lactam ring.
Benzoic acids and derivativesCHEMONTID:0000176Organic compounds containing a carboxylic acid substituent attached to a benzene ring.
ImidazopyridinonesCHEMONTID:0000177Compounds containing an imidazopyridine moiety where the pyridine ring bears a ketone group.
TriterpenoidsCHEMONTID:0001553Terpene molecules containing six isoprene units.
Tryptamines and derivativesCHEMONTID:0000183Compounds containing the tryptamine backbone, which is structurally characterized by an indole ring subsituted at the 3-position by an ethanamine.
PheniraminesCHEMONTID:0000184Compounds containing a pheniramine moiety, which is structurally characterized by the presence of a 2-benzylpyridine linked to an dimethyl(propyl)amine to form a dimethyl[3-phenyl-3-(pyridin-2-yl)propyl]amine skeleton.
PhenylmethylaminesCHEMONTID:0000185Compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
PhenethylaminesCHEMONTID:0000186Compounds containing a phenethylamine moiety, which consists of a phenyl group substituted at the second position by an ethan-1-amine.
PhenylpropylaminesCHEMONTID:0000187Compounds containing a phenylpropylamine moiety, which consists of a phenyl group substituted at the third carbon by an propan-1-amine.
PiperazinesCHEMONTID:0000189Compounds containing a piperazine ring, which is a saturated aliphatic six-member heterocyclic with two nitrogen atoms at positions 1 and 4, as well as four carbon atoms.
MethoxyphenolsCHEMONTID:0000190Compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
CyclopyrrolonesCHEMONTID:0000192Compounds belonging to a family of pyridin-2-ylpyrrole based chemicals. The pyrrole is usually fused to a benzene, pyrimidine, or dithiin.
NitrofuransCHEMONTID:0000194Compounds containing a furan ring which bears a nitro group.
1-benzothiopyransCHEMONTID:0003413Organic aromatic compounds that 1-benzothiopyran, a bicyclic compound made up of a benzene ring fused to a thiopyran, so that the sulfur atom is at the 1-position.
BenzodiazinesCHEMONTID:0004789Aromatic heterocyclic compounds containing a benzene ring fused to a diazine ring. The diazine ring is an analogue of benzene, where two carbon atoms are replaced by nitrogen atoms.
CarbazolesCHEMONTID:0000210Compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
PorphyrinsCHEMONTID:0000212Compounds containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure.
IndolizinesCHEMONTID:0000216Polycyclic compounds containing an indolizine moiety, which is characterized by the presence of a pyrrole ring fused to a pyridine(Pyrrolo[1,2-a]pyridine).
PyrazolidinesCHEMONTID:0000217Compounds containing a pyrazolidine ring, which is a five-member saturated aliphatic ring with two nitrogen atoms (at positions 1 and 2) and three carbon atoms.
HydrophenanthrenesCHEMONTID:0000223A phenanthrene derivative where at least one ring CC bond is substituted by hydrogenation.
ThiazolidinesCHEMONTID:0000226Heterocyclic compounds containing a five-member saturated aliphatic ring with one nitrogen atom, one sulfur atom, three carbon atoms.
ThiazolinesCHEMONTID:0000229Heterocyclic compounds containing a five-member unsaturated aliphatic ring with one nitrogen atom, one sulfur atom, three carbon atoms.
Organic superoxidesCHEMONTID:0000230Organic compounds containing a superoxide oxyanion.
DibenzothiepinsCHEMONTID:0000232Compounds containing a dibenzothiepin moiety, which consists of two benzene connected by a thiepine ring.
TriazolidinesCHEMONTID:0000235Compounds containing a five-member saturated aliphatic ring of two carbon atoms and three nitrogen atoms.
IndolizinoquinolinesCHEMONTID:0000239Polycyclic aromatic compounds containing an indolizine fused to a quinonline.
Purines and purine derivativesCHEMONTID:0000245Aromatic heterocyclic compounds containing a purine moiety, which is formed a pyrimidine-ring ring fused to an imidazole ring.
1,2-dioxolesCHEMONTID:0000248Organic compounds containing 1,2-dioxole, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 2, and a double bond.
ImidazolidinesCHEMONTID:0000250Organic compounds containing an imidazolidine ring, which is a saturated ring (derived from imidazole) with two nitrogen atoms at positions 1 and 3 respectively, and containing only single bonds.
Fatty acids and conjugatesCHEMONTID:0000262Aliphatic monocarboxylic acids with a saturated or unsaturated aliphatic tail (with at least 4 Carbon atoms).
Terpene glycosidesCHEMONTID:0002049Prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.
Short-chain hydroxy acids and derivativesCHEMONTID:0000266Hydroxy acids with an alkyl chain the contains less than 6 carbon atoms.
Organosulfonic acids and derivativesCHEMONTID:0000270Compounds containing a sulfonic acid or derivative, with the general structure RS(=O)2X (R=alkyl, aryl; X=any heteroatom).
1,3-dioxolesCHEMONTID:0000272Organic compounds containing 1,3-dioxole, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 3 and a double bond.
Miscellaneous metallic oxoanionic compoundsCHEMONTID:0001470Inorganic compounds containing a metallic oxoanion to which either no atom or a non metal atom is bonded.
Acryloyl compoundsCHEMONTID:0000275Organic compounds containing the acryloyl functional group (which has the core fragment but-3-en-2-one).
Aminopyridines and derivativesCHEMONTID:0000283Organic heterocyclic compounds containing an amino group attached to a pyridine ring.
Aniline and substituted anilinesCHEMONTID:0000284Organic compounds containing an aminobenzene moiety.
AnilidesCHEMONTID:0000285Organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
Organomagnesium compoundsCHEMONTID:0000287Organic compounds containing a bond between a carbon atom and magnesium atom.
ThioanisolesCHEMONTID:0000288Organic compounds in which the oxygen of an anisole has been replaced by a sulfur.
GlycerophosphoglycerolsCHEMONTID:0002216Glycerophosphoglycerols are lipids that contain two glycerol moieties that are linked to each other through the only phosphate group.
Fatty aldehydesCHEMONTID:0000298Long chain aldehydes with a chain of at least 12 carbon atoms.
Medium-chain hydroxy acids and derivativesCHEMONTID:0000299Hydroxy acids with a 6 to 12 carbon atoms long side chain.
BenzarsolesCHEMONTID:0000300Organic compounds containing a benzene ring fused to an arsole ring (five member ring containing an arsenic atom, 4 carbon atoms, and two double bonds).
PhenylpiperidinesCHEMONTID:0000303Compounds containing a phenylpiperidine skeleton, which consists of a piperidine bound to a phenyl group.
BenzothiadiazinesCHEMONTID:0000308Organic compounds containing a benzene fused to a thiadiazine ring (a six-member ring with two nitrogen atoms and a sulfur atom).
PhenothiazinesCHEMONTID:0000310Polycyclic aromatic compounds containing a phenothiazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a para-thiazine ring.
BenzopyrenesCHEMONTID:0000316Organic compounds containing a benzene fused to a pyrene(benzo[def]phenanthrene) ring system.
DibenzazepinesCHEMONTID:0000320Compounds with two benzene rings connected by an azepine ring. Azepine is an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom.
Benzoyl derivativesCHEMONTID:0000321Organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
Betaxanthins and derivativesCHEMONTID:0000322Organic compounds containing an aminoethylpyridine-2,6-dicarboxylic acid derivative.
Fatty acid estersCHEMONTID:0000324Carboxylic ester derivatives of a fatty acid.
BiphenolsCHEMONTID:0000325Organic compounds containing two phenol groups linked together by a C-C bond.
Bipyridines and oligopyridinesCHEMONTID:0000326Organic compounds containing two pyridine rings linked to each other.
BisphosphonatesCHEMONTID:0000327Organic compounds containing two phosphonate groups linked together through a carbon atoms.
PhenylazirinesCHEMONTID:0000329Compounds containing a phenylazirine moiety, which consists of an azirine ring attached to a phenyl group.
Fatty amidesCHEMONTID:0000331Carboxylic acid amide derivatives of fatty acids, that are formed from a fatty acid and an amine.
GlycerophosphoglycerophosphatesCHEMONTID:0002217Glycerophospholipids that contain two glycerophosphate skeleton linked to each other through one of the phosphate groups.
N-acylpiperidinesCHEMONTID:0000335Compounds containing an N-acyethanolamine moiety, which is characterized by an acyl group is linked to the nitrogen atom of a piperidine.
AnthocyanidinsCHEMONTID:0000336Sugar-free counterparts of anthocyanins based on the flavylium ion or 2-phenylchromenylium ion.
FlavansCHEMONTID:0000337Compounds containing a flavan moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran skeleton.
AzaborinanesCHEMONTID:0000345Organic compounds containing a six-member saturated aliphatic ring containing a nitrogen atom, an arsenic atom, and four carbon atoms.
Dicarboxylic acids and derivativesCHEMONTID:0000346Organic compounds containing exactly two carboxylic acid groups.
Organoantimony compoundsCHEMONTID:0000349Compounds containing a bond between a carbon atom and an antimony atom.
ButyrophenonesCHEMONTID:0000350Compounds containing 1-phenylbutan-1-one moiety.
CorrinoidsCHEMONTID:0000353Derivatives of the corrin nucleus, which contain four reduced or partly reduced pyrrole rings joined in a macrocycle by three =CH- groups and one direct carbon-carbon bond linking alpha positions.
CoumestansCHEMONTID:0000354Polycyclic aromatic compounds containing a coumestan moiety, which consists of a benzoxole fused to a chromen-2-one to form 1-Benzoxolo[3,2-c]chromen-6-one. They are oxidation products of pterocarpan.
CumenesCHEMONTID:0000355Aromatic compounds containing a prop-2-ylbenzene moiety.
Linear diarylheptanoidsCHEMONTID:0002651Diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain.
SesquaterpenoidsCHEMONTID:0000357Terpenoids with at least 7 consecutive isoprene units.
FuranocoumarinsCHEMONTID:0000358Polycyclic aromatic compounds containing a furan ring fused to a coumarin moiety.
Organic cyanamidesCHEMONTID:0000361Organic compounds comprising the cyanamide functional group, with the general structure R1N=C=NR2.
Organic cyanidesCHEMONTID:0004504Organic nitrogen compounds that contain the cyano (C#N) group. The group can be present either in the anionic or covalently bond form.
CyanatesCHEMONTID:0000363Organic compounds containing the cyanate functional group with the formula [OCN]-.
CyclamatesCHEMONTID:0000365Compounds containing a cyclohexylsulfamic acid moiety.
HydropyridinesCHEMONTID:0002224Compounds containing a hydrogenated pyridine ring (i.e. containing less than the maximum number of double bonds.).
MorpholinesCHEMONTID:0000392Organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
FentanylsCHEMONTID:0000372Compounds containing the fentanyl moiety or a derivative, which is based on a N-(1-(2-phenylethyl)-4-piperidinyl)-N-phenylpropanamide skeleton.
GuanidinesCHEMONTID:0000375Compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5.
ProanthocyanidinsCHEMONTID:0000379Molecules containing an oligomeric moiety of C4-C8 and/or C4-C6 and/or C2-C7 oligo/polymers of flavan-3-ols.
Benzenetriols and derivativesCHEMONTID:0001310Organic compounds containing three hydroxyl groups attached to a benzene ring.
Alloxazines and isoalloxazinesCHEMONTID:0000384Organic compounds comprising the (iso)alloxazine structure (Benzo[g]pteridine-2,4-dione).
Steroidal alkaloidsCHEMONTID:0002724Alkaloids characterized by the presence of one or more alkylamino substituents attached to a steroidal skeleton. These are azasteroids in which a nitrogen atom forms an integral part of the steroid nucleus or may be present in the side chain.
KetenesCHEMONTID:0000388Organic compounds in which a carbonyl group is connected by a double bond to an alkylidene group R2C=C=O.
IndolequinonesCHEMONTID:0000390Polycyclic compounds containing an indolequinone moiety, which consists of an indole bearing two ketones at positions 5 and 6 (or 4 and 7).
Organic nitratesCHEMONTID:0000395Organic compounds containing the nitrate oxoanion, with the formula NO3-.
Organic nitritesCHEMONTID:0000396Organic compounds containing the nitrite oxoanion, with the formula NO2-.
Nitrogen mustard compoundsCHEMONTID:0000398Compounds having two beta-haloalkyl groups bound to a nitrogen atom.
PhenylazidesCHEMONTID:0000399Compounds containing a phenylazide moiety, which consists of a linear azide substituent attached to a phenyl group.
Organoarsenic compoundsCHEMONTID:0000405Compounds containing bond between a carbon atom and an arsenic atom.
Organolithium compoundsCHEMONTID:0000406Organic compounds containing a bond between a carbon atom and lithium atom.
Organomercurial compoundsCHEMONTID:0000407Organic compounds containing a bond between a carbon atom and mercury atom.
Phosphate estersCHEMONTID:0000408Organic compounds containing phosphoric acid ester functional group, with the general structure R1P(=O)(R2)OR3. R1,R2 = O,N, or halogen atom; R3 = organyl group.
Azo compoundsCHEMONTID:0000410Derivatives of diazene(diimide), HN=NH, wherein both hydrogens are substituted by hydrocarbyl groups, e.g. PhN=NPh azobenzene or diphenyldiazene.
OximesCHEMONTID:0000411Compounds containing the oxime functional group, with the general structure R1(R2)C=NOH.
Organic peroxidesCHEMONTID:0000414Organic compounds containing the peroxide group, with the formula R1OOR2 (R1,R2=H, alkyl, aryl).
Boronic acidsCHEMONTID:0000415Compounds comprising the boronic acid functional group RB(O)O (R,R'=alkyl, aryl).
Phenoxyacetic acid derivativesCHEMONTID:0000417Compounds containing an anisole where the methane group is linked to an acetic acid or a derivative.
Phenylacetic acidsCHEMONTID:0000418Compounds containing a phenylacetic acid moiety, which consists of a phenyl group substituted at the second position by an acetic acid.
MetallotetrapyrrolesCHEMONTID:0001926Polycyclic compounds containing a tetrapyrrole skeleton combined with a metal atom.
FulminatesCHEMONTID:0000466Organic compounds containing the fulminate ion, with the formula CNO-.
Phenylcarbamic acidsCHEMONTID:0000467Compounds containing a phenylazide moiety, which consists of a carbamic acid substituent attached to a phenyl group.
AminesCHEMONTID:0002449Compounds formally derived from ammonia by replacing one, two or three hydrogen atoms by hydrocarbyl groups, and having the general structures RNH2 (primary amines), R2NH (secondary amines), R3N (tertiary amines).
Organogold compoundsCHEMONTID:0000473Organic compounds containing a bond between a carbon atom and a gold atom.
Carboxylic acid derivativesCHEMONTID:0001093Derivatives of carboxylic acid.
PolyprenolsCHEMONTID:0001535Prenols with more than 4 consecutive isoprene units.
Pyranones and derivativesCHEMONTID:0000481Compounds containing a pyran ring which bears a ketone.
SulfonylureasCHEMONTID:0000490Organic compounds containing a sulfonyl group with the structure R-S(=O)2-R', where R' is an urea.
Isoflav-2-enesCHEMONTID:0002901Flavonoids with a structure based on the 3-phenylchromene skeleton, with a double bond between the C2 and C3 carbon atoms of the chromene moiety.
AminalsCHEMONTID:0000497Compounds having two amino groups bonded to the same carbon, R2C(NR2)2 where R can by a hydrogen or an alkyl group.
ImidoestersCHEMONTID:0000499Organic ester derivatives of imidic acid. They have the general structure ROC(CR')=NR\", where R=organyl group, R'-R\"= H or organyl group.
IsocyanatesCHEMONTID:0000501Organic compounds containing the isocyanic acid tautomer, HN=C=O, of cyanic acid, HOC#N or its hydrocarbyl derivatives RN=C=O.
Quaternary ammonium saltsCHEMONTID:0000503Compounds containing positively charged polyatomic ion of the structure NR4+, R being an alkyl group or an aryl group.
Lineolic acids and derivativesCHEMONTID:0000504Derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.
SulfonesCHEMONTID:0000505Compounds containing a sulfonyl group( which as the general structure RS(=O)2R' (R,R' =alkyl, aryl)) attached to two carbon atoms.
Isoflavonoid O-glycosidesCHEMONTID:0000507O-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.
UreasCHEMONTID:0000517Compounds containing two amine groups joined by a carbonyl (C=O) functional group.
TriphenylenesCHEMONTID:0000518Compounds containing a triphenylene moiety, which consists of four fused benzene rings forming a 9,10-benzo[l]phenanthrene.
Actinide hydridesCHEMONTID:0000520Inorganic hydride compounds in which the heaviest metal atom is an actinide.
Actinide nitridesCHEMONTID:0000521Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest metal atom is an actinide.
Actinide oxidesCHEMONTID:0000522Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is an actinide.
Actinide sulfidesCHEMONTID:0000523Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is an actinide.
Alkali metal hydridesCHEMONTID:0000524Inorganic hydride compounds in which the heaviest metal atom is an alkali metal.
Alkali metal nitridesCHEMONTID:0000525Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest metal atom is an alkali metal.
Alkali metal oxidesCHEMONTID:0000526Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is an alkali metal.
Alkali metal sulfidesCHEMONTID:0000527Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is an alkali metal.
Post-transition metal hydridesCHEMONTID:0000528Inorganic hydride compounds in which the heaviest metal atom is a post-transition metal.
Post-transition metal nitridesCHEMONTID:0000529Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest metal atom is a post-transition metal.
Post-transition metal oxidesCHEMONTID:0000530Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a post-transition metal.
Post-transition metal sulfidesCHEMONTID:0000531Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a post-transition metal.
Metalloid hydridesCHEMONTID:0000532Inorganic hydride compounds in which the heaviest metal atom is a metalloid.
Metalloid nitridesCHEMONTID:0000533Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest metal atom is a metalloid.
Metalloid oxidesCHEMONTID:0000534Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a metalloid.
Metalloid sulfidesCHEMONTID:0000535Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a metalloid.
Transition metal hydridesCHEMONTID:0000536Inorganic hydride compounds in which the heaviest metal atom is a transition metal.
Transition metal nitridesCHEMONTID:0000537Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest metal atom is a transition metal.
Transition metal oxidesCHEMONTID:0000538Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a transition metal.
Transition metal sulfidesCHEMONTID:0000539Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a transition metal.
Lanthanide hydridesCHEMONTID:0000540Inorganic halogenic compounds in which the heaviest metal atom is a lanthanide.
Lanthanide nitridesCHEMONTID:0000541Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest metal atom is a lanthanide.
Lanthanide oxidesCHEMONTID:0000542Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a lanthanide.
Lanthanide sulfidesCHEMONTID:0000543Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a lanthanide.
Alkaline earth metal hydridesCHEMONTID:0000544Inorganic halogenic compounds in which the heaviest metal atom is an alkaline earth metal.
Alkaline earth metal nitridesCHEMONTID:0000545Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of −3, and the heaviest metal atom is an alkaline earth metal.
Alkaline earth metal oxidesCHEMONTID:0000546Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is an alkaline earth metal.
Alkaline earth metal sulfidesCHEMONTID:0000547Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is an alkaline earth metal.
Halogen hydridesCHEMONTID:0000548Inorganic compounds in which the heaviest atom bonded to a hydrogen atom is a halogen.
Halogen nitridesCHEMONTID:0000549Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of -3, and the heaviest atom bonded to it is a halogen.
Halogen oxidesCHEMONTID:0000550Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a halogen.
Halogen sulfidesCHEMONTID:0000551Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen is a halogen.
Other non-metal hydridesCHEMONTID:0000552Inorganic compounds in which the heaviest atom bonded to a hydrogen atom is belongs to the class of 'other non-metals'.
Other non-metal nitridesCHEMONTID:0000553Inorganic compounds of nitrogen where nitrogen has a formal oxidation state of −3, and the heaviest atom bonded to it belongs to the class of 'other non-metals'.
Other non-metal oxidesCHEMONTID:0000554Inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen belongs to the class of 'other non-metals'.
Other non-metal sulfidesCHEMONTID:0000555Inorganic compounds containing a sulfur atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen belongs to the class of other non-metals.
Actinide astatidesCHEMONTID:0000556Inorganic compounds in which the largest halogen atom is Astatine, and the heaviest metal atom is an actinide.
Actinide bromidesCHEMONTID:0000557Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom an actinide.
Actinide chloridesCHEMONTID:0000558Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is an actinide.
Actinide fluoridesCHEMONTID:0000559Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is an actinide.
Actinide iodidesCHEMONTID:0000560Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is an actinide.
Alkali metal astatidesCHEMONTID:0000561Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is an alkali metal.
Alkali metal bromidesCHEMONTID:0000562Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom an alkali metal.
Alkali metal chloridesCHEMONTID:0000563Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is an alkali metal.
Alkali metal fluoridesCHEMONTID:0000564Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is an alkali metal.
Alkali metal iodidesCHEMONTID:0000565Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is an alkali metal.
Alkaline earth metal astatidesCHEMONTID:0000566Inorganic compounds in which the largest halogen atom is Astatine, and the heaviest metal atom is a lanthanide.
Alkaline earth metal bromidesCHEMONTID:0000567Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom a lanthanide.
Alkaline earth metal chloridesCHEMONTID:0000568Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is a lanthanide.
Alkaline earth metal fluoridesCHEMONTID:0000569Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is a lanthanide.
Alkaline earth metal iodidesCHEMONTID:0000570Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is an alkaline earth metal.
Post-transition metal astatidesCHEMONTID:0000571Inorganic compounds in which the largest halogen atom is Astatine, and the heaviest metal atom is a post-transition metal.
Post-transition metal bromidesCHEMONTID:0000572Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom a post-transition metal.
Post-transition metal chloridesCHEMONTID:0000573Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is a post-transition metal.
Post-transition metal fluoridesCHEMONTID:0000574Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is a post-transition metal.
Post-transition metal iodidesCHEMONTID:0000575Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is a post-transition metal.
Lanthanide astatidesCHEMONTID:0000576Inorganic compounds in which the largest halogen atom is Astatine, and the heaviest metal atom is a lanthanide.
Lanthanide bromidesCHEMONTID:0000577Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom a lanthanide.
Lanthanide chloridesCHEMONTID:0000578Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is a lanthanide.
Lanthanide fluoridesCHEMONTID:0000579Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is a lanthanide.
Lanthanide iodidesCHEMONTID:0000580Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is a lanthanide.
Metalloid astatidesCHEMONTID:0000581Inorganic compounds in which the largest halogen atom is Astatine, and the heaviest metal atom is a metalloid.
Metalloid bromidesCHEMONTID:0000582Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom a metalloid.
Metalloid chloridesCHEMONTID:0000583Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is a metalloid.
Metalloid fluoridesCHEMONTID:0000584Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is a metalloid.
Metalloid iodidesCHEMONTID:0000585Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is a metalloid.
Transition metal astatidesCHEMONTID:0000586Inorganic compounds in which the largest halogen atom is Astatine, and the heaviest metal atom is a transition metal.
Transition metal bromidesCHEMONTID:0000587Inorganic compounds in which the largest halogen atom is Bromine, and the heaviest metal atom a transition metal.
Transition metal chloridesCHEMONTID:0000588Inorganic compounds in which the largest halogen atom is Chlorine, and the heaviest metal atom is a transition metal.
Transition metal fluoridesCHEMONTID:0000589Inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is a transition metal.
Transition metal iodidesCHEMONTID:0000590Inorganic compounds in which the largest halogen atom is Iodine, and the heaviest metal atom is a transition metal.
Actinide bromatesCHEMONTID:0000591Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide chloratesCHEMONTID:0000592Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide chloritesCHEMONTID:0000593Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide chromatesCHEMONTID:0000594Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is an actinide.
Actinide chromitesCHEMONTID:0000595Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide cyanatesCHEMONTID:0000596Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide hydroxidesCHEMONTID:0000598Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide hypobromitesCHEMONTID:0000599Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide hypochloritesCHEMONTID:0000600Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide hyponitritesCHEMONTID:0000601Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide hypophosphitesCHEMONTID:0000602Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide iodatesCHEMONTID:0000603Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide nitritesCHEMONTID:0000604Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide nitratesCHEMONTID:0000605Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide orthonitratesCHEMONTID:0000606Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide perbromatesCHEMONTID:0000607Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide perchloratesCHEMONTID:0000608Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide periodatesCHEMONTID:0000609Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide permanganatesCHEMONTID:0000610Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide peroxynitratesCHEMONTID:0000611Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide peroxynitritesCHEMONTID:0000612Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide perrhenatesCHEMONTID:0000613Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide pertechnetatesCHEMONTID:0000614Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide phosphitesCHEMONTID:0000615Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide phosphatesCHEMONTID:0000616Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide pyrophosphatesCHEMONTID:0000617Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide selenatesCHEMONTID:0000618Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide selenitesCHEMONTID:0000619Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide sulfatesCHEMONTID:0000620Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide sulfitesCHEMONTID:0000621Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide superoxidesCHEMONTID:0000622Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide peroxomonosulfatesCHEMONTID:0000624Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide peroxodisulfatesCHEMONTID:0000625Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide pyrosulfatesCHEMONTID:0000626Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide tetrathionatesCHEMONTID:0000627Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide thiosulfatesCHEMONTID:0000628Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide dithionitesCHEMONTID:0000629Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide hyposulfitesCHEMONTID:0000630Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is an actinide.
Alkali metal bromatesCHEMONTID:0000631Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal chloratesCHEMONTID:0000632Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal chloritesCHEMONTID:0000633Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal chromatesCHEMONTID:0000634Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is an alkali metal.
Alkali metal chromitesCHEMONTID:0000635Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal cyanatesCHEMONTID:0000636Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is an alkali metal.
GlycosylglycerolsCHEMONTID:0000637Glycerolipids structurally characterized by the presence of one or more sugar residues attached to glycerol via a glycosidic linkage.
Alkali metal hydroxidesCHEMONTID:0000638Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal hypobromitesCHEMONTID:0000639Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal hypochloritesCHEMONTID:0000640Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal hyponitritesCHEMONTID:0000641Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal hypophosphitesCHEMONTID:0000642Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal iodatesCHEMONTID:0000643Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal nitritesCHEMONTID:0000644Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal nitratesCHEMONTID:0000645Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal orthonitratesCHEMONTID:0000646Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal perbromatesCHEMONTID:0000647Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal perchloratesCHEMONTID:0000648Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal periodatesCHEMONTID:0000649Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal permanganatesCHEMONTID:0000650Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal peroxynitratesCHEMONTID:0000651Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal peroxynitritesCHEMONTID:0000652Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal perrhenatesCHEMONTID:0000653Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal pertechnetatesCHEMONTID:0000654Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal phosphitesCHEMONTID:0000655Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal phosphatesCHEMONTID:0000656Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal pyrophosphatesCHEMONTID:0000657Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal selenatesCHEMONTID:0000658Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal selenitesCHEMONTID:0000659Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal sulfatesCHEMONTID:0000660Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal sulfitesCHEMONTID:0000661Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal superoxidesCHEMONTID:0000662Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal peroxomonosulfatesCHEMONTID:0000664Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal peroxodisulfatesCHEMONTID:0000665Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal pyrosulfatesCHEMONTID:0000666Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal tetrathionatesCHEMONTID:0000667Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal thiosulfatesCHEMONTID:0000668Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal dithionitesCHEMONTID:0000669Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal hyposulfitesCHEMONTID:0000670Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkaline earth metal bromatesCHEMONTID:0000671Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal chloratesCHEMONTID:0000672Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal chloritesCHEMONTID:0000673Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal chromatesCHEMONTID:0000674Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is a lanthanide.
Alkaline earth metal cyanatesCHEMONTID:0000675Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal hydroxidesCHEMONTID:0000677Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal hypobromitesCHEMONTID:0000678Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal hypochloritesCHEMONTID:0000679Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal hyponitritesCHEMONTID:0000680Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal hypophosphitesCHEMONTID:0000681Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal iodatesCHEMONTID:0000682Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal nitritesCHEMONTID:0000683Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal nitratesCHEMONTID:0000684Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal orthonitratesCHEMONTID:0000685Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal perbromatesCHEMONTID:0000686Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal perchloratesCHEMONTID:0000687Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal periodatesCHEMONTID:0000688Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal permanganatesCHEMONTID:0000689Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal peroxynitratesCHEMONTID:0000690Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal peroxynitritesCHEMONTID:0000691Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal perrhenatesCHEMONTID:0000692Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal pertechnetatesCHEMONTID:0000693Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal phosphitesCHEMONTID:0000694Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal phosphatesCHEMONTID:0000695Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal pyrophosphatesCHEMONTID:0000696Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal selenatesCHEMONTID:0000697Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal selenitesCHEMONTID:0000698Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal sulfatesCHEMONTID:0000699Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal sulfitesCHEMONTID:0000700Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal superoxidesCHEMONTID:0000701Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Terpene lactonesCHEMONTID:0001283Prenol lipids containing a lactone ring.
Alkaline earth metal peroxomonosulfatesCHEMONTID:0000703Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal peroxodisulfatesCHEMONTID:0000704Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal pyrosulfatesCHEMONTID:0000705Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal tetrathionatesCHEMONTID:0000706Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal thiosulfatesCHEMONTID:0000707Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal dithionitesCHEMONTID:0000708Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal hyposulfitesCHEMONTID:0000709Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Post-transition metal bromatesCHEMONTID:0000710Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal chloratesCHEMONTID:0000711Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal chloritesCHEMONTID:0000712Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal chromatesCHEMONTID:0000713Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is a post-transition metal.
Post-transition metal chromitesCHEMONTID:0000714Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal cyanatesCHEMONTID:0000715Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
ChlorinsCHEMONTID:0000716Large heterocyclic aromatic ring systems consisting, at the core, of three pyrroles and one pyrroline coupled through four methine linkages.
Post-transition metal hydroxidesCHEMONTID:0000717Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal hypobromitesCHEMONTID:0000718Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal hypochloritesCHEMONTID:0000719Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal hyponitritesCHEMONTID:0000720Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal hypophosphitesCHEMONTID:0000721Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal iodatesCHEMONTID:0000722Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal nitritesCHEMONTID:0000723Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal nitratesCHEMONTID:0000724Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal orthonitratesCHEMONTID:0000725Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal perbromatesCHEMONTID:0000726Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal perchloratesCHEMONTID:0000727Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal periodatesCHEMONTID:0000728Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal permanganatesCHEMONTID:0000729Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal peroxynitratesCHEMONTID:0000730Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal peroxynitritesCHEMONTID:0000731Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal perrhenatesCHEMONTID:0000732Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal pertechnetatesCHEMONTID:0000733Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal phosphitesCHEMONTID:0000734Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal phosphatesCHEMONTID:0000735Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal pyrophosphatesCHEMONTID:0000736Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal selenatesCHEMONTID:0000737Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal selenitesCHEMONTID:0000738Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal sulfatesCHEMONTID:0000739Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal sulfitesCHEMONTID:0000740Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal superoxidesCHEMONTID:0000741Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is a post-transition metal.
PhospholanesCHEMONTID:0000742Compounds containing a phospholane ring, which is a five-member saturated aliphatic heterocycle with one phosphorus atom and four carbon atoms.
Post-transition metal peroxomonosulfatesCHEMONTID:0000743Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal peroxodisulfatesCHEMONTID:0000744Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal pyrosulfatesCHEMONTID:0000745Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal tetrathionatesCHEMONTID:0000746Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal thiosulfatesCHEMONTID:0000747Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal dithionitesCHEMONTID:0000748Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal hyposulfitesCHEMONTID:0000749Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Lanthanide bromatesCHEMONTID:0000750Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide chloratesCHEMONTID:0000751Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide chloritesCHEMONTID:0000752Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide chromatesCHEMONTID:0000753Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is a lanthanide.
Lanthanide chromitesCHEMONTID:0000754Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide cyanatesCHEMONTID:0000755Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide hydroxidesCHEMONTID:0000757Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide hypobromitesCHEMONTID:0000758Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide hypochloritesCHEMONTID:0000759Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide hyponitritesCHEMONTID:0000760Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide hypophosphitesCHEMONTID:0000761Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide iodatesCHEMONTID:0000762Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide nitritesCHEMONTID:0000763Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide nitratesCHEMONTID:0000764Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide orthonitratesCHEMONTID:0000765Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide perbromatesCHEMONTID:0000766Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide perchloratesCHEMONTID:0000767Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide periodatesCHEMONTID:0000768Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide permanganatesCHEMONTID:0000769Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide peroxynitratesCHEMONTID:0000770Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide peroxynitritesCHEMONTID:0000771Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide perrhenatesCHEMONTID:0000772Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide pertechnetatesCHEMONTID:0000773Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide phosphitesCHEMONTID:0000774Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide phosphatesCHEMONTID:0000775Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide pyrophosphatesCHEMONTID:0000776Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide selenatesCHEMONTID:0000777Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide selenitesCHEMONTID:0000778Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide sulfatesCHEMONTID:0000779Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide sulfitesCHEMONTID:0000780Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide superoxidesCHEMONTID:0000781Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide peroxomonosulfatesCHEMONTID:0000783Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide peroxodisulfatesCHEMONTID:0000784Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide pyrosulfatesCHEMONTID:0000785Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide tetrathionatesCHEMONTID:0000786Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide thiosulfatesCHEMONTID:0000787Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide dithionitesCHEMONTID:0000788Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide hyposulfitesCHEMONTID:0000789Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Metalloid bromatesCHEMONTID:0000790Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid chloratesCHEMONTID:0000791Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid chloritesCHEMONTID:0000792Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid chromatesCHEMONTID:0000793Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is a metalloid.
Metalloid chromitesCHEMONTID:0000794Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid cyanatesCHEMONTID:0000795Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid hydroxidesCHEMONTID:0000797Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid hypobromitesCHEMONTID:0000798Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid hypochloritesCHEMONTID:0000799Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid hyponitritesCHEMONTID:0000800Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid hypophosphitesCHEMONTID:0000801Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid iodatesCHEMONTID:0000802Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid nitritesCHEMONTID:0000803Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid nitratesCHEMONTID:0000804Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid orthonitratesCHEMONTID:0000805Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid perbromatesCHEMONTID:0000806Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid perchloratesCHEMONTID:0000807Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid periodatesCHEMONTID:0000808Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid permanganatesCHEMONTID:0000809Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid peroxynitratesCHEMONTID:0000810Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid peroxynitritesCHEMONTID:0000811Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid perrhenatesCHEMONTID:0000812Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid pertechnetatesCHEMONTID:0000813Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid phosphitesCHEMONTID:0000814Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid phosphatesCHEMONTID:0000815Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid pyrophosphatesCHEMONTID:0000816Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid selenatesCHEMONTID:0000817Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid selenitesCHEMONTID:0000818Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid sulfatesCHEMONTID:0000819Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid sulfitesCHEMONTID:0000820Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Metalloid superoxidesCHEMONTID:0000821Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid peroxomonosulfatesCHEMONTID:0000823Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid peroxodisulfatesCHEMONTID:0000824Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid pyrosulfatesCHEMONTID:0000825Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid tetrathionatesCHEMONTID:0000826Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid thiosulfatesCHEMONTID:0000827Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid dithionitesCHEMONTID:0000828Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid hyposulfitesCHEMONTID:0000829Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is a metalloid.
Transition metal bromatesCHEMONTID:0000830Inorganic compounds in which the largest oxoanion is bromate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal chloratesCHEMONTID:0000831Inorganic compounds in which the largest oxoanion is chlorate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal chloritesCHEMONTID:0000832Inorganic compounds in which the largest oxoanion is chlorite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal chromatesCHEMONTID:0000833Inorganic compounds in which the largest oxoanion is chromate, and in which the heaviest atom is a transition metal.
Transition metal chromitesCHEMONTID:0000834Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal cyanatesCHEMONTID:0000835Inorganic compounds in which the largest oxoanion is cyanate, and in which the heaviest atom not in an oxoanion is a transition metal.
ImidazodithiazolethionesCHEMONTID:0000836Organic compounds containing an imidazole ring fused to a dithiazolethione ring.
Transition metal hydroxidesCHEMONTID:0000837Inorganic compounds in which the largest oxoanion is hydroxide, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal hypobromitesCHEMONTID:0000838Inorganic compounds in which the largest oxoanion is hypobromite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal hypochloritesCHEMONTID:0000839Inorganic compounds in which the largest oxoanion is hypochlorite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal hyponitritesCHEMONTID:0000840Inorganic compounds in which the largest oxoanion is hyponitrite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal hypophosphitesCHEMONTID:0000841Inorganic compounds in which the largest oxoanion is hypophosphite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal iodatesCHEMONTID:0000842Inorganic compounds in which the largest oxoanion is iodate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal nitratesCHEMONTID:0000843Inorganic compounds in which the largest oxoanion is nitrate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal orthonitratesCHEMONTID:0000844Inorganic compounds in which the largest oxoanion is orthonitrate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal perbromatesCHEMONTID:0000845Inorganic compounds in which the largest oxoanion is perbromate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal perchloratesCHEMONTID:0000846Inorganic compounds in which the largest oxoanion is perchlorate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal periodatesCHEMONTID:0000847Inorganic compounds in which the largest oxoanion is periodate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal permanganatesCHEMONTID:0000848Inorganic compounds in which the largest oxoanion is permanganate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal peroxynitratesCHEMONTID:0000849Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal peroxynitritesCHEMONTID:0000850Inorganic compounds in which the largest oxoanion is peroxynitrate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal perrhenatesCHEMONTID:0000851Inorganic compounds in which the largest oxoanion is perhenate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal pertechnetatesCHEMONTID:0000852Inorganic compounds in which the largest oxoanion is pertechnetate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal phosphitesCHEMONTID:0000853Inorganic compounds in which the largest oxoanion is phosphite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal phosphatesCHEMONTID:0000854Inorganic compounds in which the largest oxoanion is phosphate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal pyrophosphatesCHEMONTID:0000855Inorganic compounds in which the largest oxoanion is pyrophosphate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal selenatesCHEMONTID:0000856Inorganic compounds in which the largest oxoanion is selenate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal selenitesCHEMONTID:0000857Inorganic compounds in which the largest oxoanion is selenite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal sulfatesCHEMONTID:0000858Inorganic compounds in which the largest oxoanion is sulfate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal sulfitesCHEMONTID:0000859Inorganic compounds in which the largest oxoanion is sulfite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal superoxidesCHEMONTID:0000860Inorganic compounds in which the largest oxoanion is superoxide, and in which the heaviest atom not in an oxoanion is a transition metal.
PhospholesCHEMONTID:0000861Compounds containing a phosphole ring, which is a five-member aromatic heterocycle with one phosphorus atom and four carbon atoms.
Transition metal peroxomonosulfatesCHEMONTID:0000862Inorganic compounds in which the largest oxoanion is peroxomonosulfate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal peroxodisulfatesCHEMONTID:0000863Inorganic compounds in which the largest oxoanion is peroxodisulfate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal pyrosulfatesCHEMONTID:0000864Inorganic compounds in which the largest oxoanion is pyrosulfate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal tetrathionatesCHEMONTID:0000865Inorganic compounds in which the largest oxoanion is tetrathionate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal thiosulfatesCHEMONTID:0000866Inorganic compounds in which the largest oxoanion is thiosulfate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal dithionitesCHEMONTID:0000867Inorganic compounds in which the largest oxoanion is dithionite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal hyposulfitesCHEMONTID:0000868Inorganic compounds in which the largest oxoanion is hyposulfite, and in which the heaviest atom not in an oxoanion is a transition metal.
Actinide aluminatesCHEMONTID:0000869Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide antimonatesCHEMONTID:0000870Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide antimonitesCHEMONTID:0000871Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide arsenatesCHEMONTID:0000872Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide arsenitesCHEMONTID:0000873Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide bisulfitesCHEMONTID:0000874Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide boratesCHEMONTID:0000875Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide ferratesCHEMONTID:0000876Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide manganatesCHEMONTID:0000877Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide molybdatesCHEMONTID:0000878Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide plumbatesCHEMONTID:0000879Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide plumbitesCHEMONTID:0000880Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide silicatesCHEMONTID:0000881Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide stannatesCHEMONTID:0000882Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide stannitesCHEMONTID:0000883Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide telluratesCHEMONTID:0000884Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide telluritesCHEMONTID:0000885Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide tetrahydroxyboratesCHEMONTID:0000886Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide tungstatesCHEMONTID:0000887Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide orthovanadatesCHEMONTID:0000888Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is an actinide.
Alkali metal aluminatesCHEMONTID:0000889Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal antimonatesCHEMONTID:0000890Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal antimonitesCHEMONTID:0000891Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal arsenatesCHEMONTID:0000892Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal arsenitesCHEMONTID:0000893Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal bisulfitesCHEMONTID:0000894Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal boratesCHEMONTID:0000895Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal ferratesCHEMONTID:0000896Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal manganatesCHEMONTID:0000897Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal molybdatesCHEMONTID:0000898Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal plumbatesCHEMONTID:0000899Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal plumbitesCHEMONTID:0000900Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal silicatesCHEMONTID:0000901Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal stannatesCHEMONTID:0000902Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal stannitesCHEMONTID:0000903Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal telluratesCHEMONTID:0000904Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal telluritesCHEMONTID:0000905Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal tetrahydroxyboratesCHEMONTID:0000906Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal tungstatesCHEMONTID:0000907Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal orthovanadatesCHEMONTID:0000908Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkaline earth metal aluminatesCHEMONTID:0000909Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal antimonatesCHEMONTID:0000910Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal antimonitesCHEMONTID:0000911Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal arsenatesCHEMONTID:0000912Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal arsenitesCHEMONTID:0000913Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal bisulfitesCHEMONTID:0000914Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal boratesCHEMONTID:0000915Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal ferratesCHEMONTID:0000916Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Alkaline earth metal manganatesCHEMONTID:0000917Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal molybdatesCHEMONTID:0000918Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal plumbatesCHEMONTID:0000919Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal plumbitesCHEMONTID:0000920Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal silicatesCHEMONTID:0000921Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal stannatesCHEMONTID:0000922Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal stannitesCHEMONTID:0000923Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal telluratesCHEMONTID:0000924Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal telluritesCHEMONTID:0000925Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal tetrahydroxyboratesCHEMONTID:0000926Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal tungstatesCHEMONTID:0000927Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal orthovanadatesCHEMONTID:0000928Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Post-transition metal aluminatesCHEMONTID:0000929Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal antimonatesCHEMONTID:0000930Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal antimonitesCHEMONTID:0000931Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal arsenatesCHEMONTID:0000932Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal arsenitesCHEMONTID:0000933Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal bisulfitesCHEMONTID:0000934Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal boratesCHEMONTID:0000935Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal ferratesCHEMONTID:0000936Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal manganatesCHEMONTID:0000937Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal molybdatesCHEMONTID:0000938Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal plumbatesCHEMONTID:0000939Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal plumbitesCHEMONTID:0000940Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal silicatesCHEMONTID:0000941Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal stannatesCHEMONTID:0000942Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal stannitesCHEMONTID:0000943Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal telluratesCHEMONTID:0000944Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal telluritesCHEMONTID:0000945Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal tetrahydroxyboratesCHEMONTID:0000946Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal tungstatesCHEMONTID:0000947Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal orthovanadatesCHEMONTID:0000948Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Lanthanide aluminatesCHEMONTID:0000949Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide antimonatesCHEMONTID:0000950Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide antimonitesCHEMONTID:0000951Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide arsenatesCHEMONTID:0000952Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide arsenitesCHEMONTID:0000953Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide bisulfitesCHEMONTID:0000954Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide boratesCHEMONTID:0000955Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide ferratesCHEMONTID:0000956Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide manganatesCHEMONTID:0000957Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide molybdatesCHEMONTID:0000958Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide plumbatesCHEMONTID:0000959Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide plumbitesCHEMONTID:0000960Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide silicatesCHEMONTID:0000961Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide stannatesCHEMONTID:0000962Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide stannitesCHEMONTID:0000963Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide telluratesCHEMONTID:0000964Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide telluritesCHEMONTID:0000965Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide tetrahydroxyboratesCHEMONTID:0000966Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide tungstatesCHEMONTID:0000967Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide orthovanadatesCHEMONTID:0000968Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Metalloid aluminatesCHEMONTID:0000969Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is a metalloid metal.
Metalloid antimonatesCHEMONTID:0000970Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid antimonitesCHEMONTID:0000971Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid arsenatesCHEMONTID:0000972Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Metalloid arsenitesCHEMONTID:0000973Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid bisulfitesCHEMONTID:0000974Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid boratesCHEMONTID:0000975Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid ferratesCHEMONTID:0000976Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid manganatesCHEMONTID:0000977Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid molybdatesCHEMONTID:0000978Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid plumbatesCHEMONTID:0000979Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid silicatesCHEMONTID:0000980Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid stannatesCHEMONTID:0000981Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid stannitesCHEMONTID:0000982Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid telluratesCHEMONTID:0000983Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid telluritesCHEMONTID:0000984Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid tetrahydroxyboratesCHEMONTID:0000985Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid tungstatesCHEMONTID:0000986Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid orthovanadatesCHEMONTID:0000987Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is a metalloid.
Transition metal aluminatesCHEMONTID:0000988Inorganic compounds in which the largest oxoanion is aluminate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal antimonatesCHEMONTID:0000989Inorganic compounds in which the largest oxoanion is antimonate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal antimonitesCHEMONTID:0000990Inorganic compounds in which the largest oxoanion is antimonite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal arsenatesCHEMONTID:0000991Inorganic compounds in which the largest oxoanion is arsenate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal arsenitesCHEMONTID:0000992Inorganic compounds in which the largest oxoanion is arsenite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal bisulfitesCHEMONTID:0000993Inorganic compounds in which the largest oxoanion is bisulfite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal boratesCHEMONTID:0000994Inorganic compounds in which the largest oxoanion is borate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal manganatesCHEMONTID:0000995Inorganic compounds in which the largest oxoanion is manganate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal molybdatesCHEMONTID:0000996Inorganic compounds in which the largest oxoanion is molybdate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal plumbatesCHEMONTID:0000997Inorganic compounds in which the largest oxoanion is plumbate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal plumbitesCHEMONTID:0000998Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal silicatesCHEMONTID:0000999Inorganic compounds in which the largest oxoanion is silicate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal stannatesCHEMONTID:0001000Inorganic compounds in which the largest oxoanion is stannate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal stannitesCHEMONTID:0001001Inorganic compounds in which the largest oxoanion is stannite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal telluratesCHEMONTID:0001002Inorganic compounds in which the largest oxoanion is tellurate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal telluritesCHEMONTID:0001003Inorganic compounds in which the largest oxoanion is tellurite, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal tetrahydroxyboratesCHEMONTID:0001004Inorganic compounds in which the largest oxoanion is tetrahydroxyborate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal tungstatesCHEMONTID:0001005Inorganic compounds in which the largest oxoanion is tungstate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal orthovanadatesCHEMONTID:0001006Inorganic compounds in which the largest oxoanion is orthovanadate, and in which the heaviest atom not in an oxoanion is a transition metal.
Steroidal glycosidesCHEMONTID:0001013Sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.
CycloalkanesCHEMONTID:0001016Saturated monocyclic hydrocarbons (with or without side chains).
Acyl bromidesCHEMONTID:0001017Organic compounds containing the functional group -CO-Br.
Acyl chloridesCHEMONTID:0001022Organic compounds containing the functional group -CO-Cl.
Acyl fluoridesCHEMONTID:0001023Organic compounds containing the functional group -CO-F.
Acyl iodidesCHEMONTID:0001024Organic compounds containing the functional group -CO-I.
Alkyl bromidesCHEMONTID:0001025Organic compounds containing the alkyl bromide functional group with formula R-Br, where R is an alkyl group.
Alkyl chloridesCHEMONTID:0001026Organic compounds containing the alkyl chloride functional group with formula R-Cl , where R is an alkyl group.
Alkyl fluoridesCHEMONTID:0001027Organic compounds containing the alkyl fluoride functional group with formula R-F , where R is an alkyl group.
Alkyl iodidesCHEMONTID:0001028Organic compounds containing the alkyl iodide functional group with formula R-I , where R is an alkyl group.
Aryl bromidesCHEMONTID:0001029Organic compounds containing the acyl bromide functional group.
Aryl chloridesCHEMONTID:0001030Organic compounds containing the acyl chloride functional group.
Aryl fluoridesCHEMONTID:0001031Organic compounds containing the acyl fluoride functional group.
Aryl iodidesCHEMONTID:0001032Organic compounds containing the acyl iodide functional group.
Imidoyl bromidesCHEMONTID:0001033Imidoyl halides with the general formula R(Br)C=NR' where X is a bromine atom.
Imidoyl chloridesCHEMONTID:0001034Imidoyl halides with the general formula R(Br)C=NR' where X is a chlorine atom.
Imidoyl fluoridesCHEMONTID:0001035Imidoyl halides with the general formula R(Br)C=NR' where X is a fluorine atom.
Imidoyl iodidesCHEMONTID:0001036Imidoyl halides with the general formula R(Br)C=NR' where X is a iodine atom.
Organic sulfuryl bromidesCHEMONTID:0001037Organic compounds containing the sulfuryl bromide functional group.
Organic sulfuryl chloridesCHEMONTID:0001038Organic compounds containing the sulfuryl chloride functional group.
Organic sulfuryl fluoridesCHEMONTID:0001039Organic compounds containing the sulfuryl fluoride functional group.
Organic sulfuryl iodidesCHEMONTID:0001040Organic compounds containing the sulfuryl iodide functional group.
Sulfonyl bromidesCHEMONTID:0001041Compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to a bromine atom.
Sulfonyl chloridesCHEMONTID:0001042Compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to a chlorine atom.
Sulfonyl fluoridesCHEMONTID:0001043Compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to a fluorine atom.
Sulfonyl iodidesCHEMONTID:0001044Compounds containing a sulfonyl (R-S(=O)2-R') functional group singly bonded to an iodine atom.
Non-metal bromatesCHEMONTID:0001048Inorganic non-metallic compounds containing a bromate as its largest oxoanion.
Non-metal chloratesCHEMONTID:0001049Inorganic non-metallic compounds containing a chlorate as its largest oxoanion.
Non-metal chloritesCHEMONTID:0001050Inorganic non-metallic compounds containing a chlorite as its largest oxoanion.
Non-metal chromatesCHEMONTID:0001051Inorganic non-metallic compounds containing a chromate as its largest oxoanion.
Non-metal chromitesCHEMONTID:0001052Inorganic non-metallic compounds containing a chromite as its largest oxoanion.
Non-metal cyanatesCHEMONTID:0001053Inorganic non-metallic compounds containing a cyanate as its largest oxoanion.
Non-metal hydroxidesCHEMONTID:0001055Inorganic non-metallic compounds containing the hydroxide group as its largest oxoanion.
Non-metal hypobromitesCHEMONTID:0001056Inorganic non-metallic compound scontaining a hypobromite as its largest oxoanion.
Non-metal hypochloritesCHEMONTID:0001057Inorganic non-metallic compounds containing a hypochlorite as its largest oxoanion.
Non-metal hyponitritesCHEMONTID:0001058Inorganic non-metallic compounds containing a hyponitrite as its largest oxoanion.
Non-metal hypophosphitesCHEMONTID:0001059Inorganic non-metallic compounds containing a hypophosphite as its largest oxoanion.
Non-metal iodatesCHEMONTID:0001060Inorganic non-metallic compounds containing a iodate as its largest oxoanion.
Non-metal nitritesCHEMONTID:0001061Inorganic non-metallic compounds containing a nitrite as its largest oxoanion.
Non-metal nitratesCHEMONTID:0001062Inorganic non-metallic compoundscontaining a nitrate as its largest oxoanion.
Non-metal orthonitratesCHEMONTID:0001063Inorganic non-metallic compoundscontaining a orthonitrate as its largest oxoanion.
Non-metal perbromatesCHEMONTID:0001064Inorganic non-metallic compoundscontaining a perbromate as its largest oxoanion.
Non-metal perchloratesCHEMONTID:0001065Inorganic non-metallic compoundscontaining a perchlorate as its largest oxoanion.
Non-metal periodatesCHEMONTID:0001066Inorganic non-metallic compoundscontaining a periodate as its largest oxoanion.
Non-metal permanganatesCHEMONTID:0001067Inorganic non-metallic compounds containing a permanganate as its largest oxoanion.
Non-metal peroxynitratesCHEMONTID:0001068Inorganic non-metallic compoundscontaining a peroxynitrate as its largest oxoanion.
Non-metal peroxynitritesCHEMONTID:0001069Inorganic non-metallic compoundscontaining a peroxynitrite as its largest oxoanion.
Non-metal perrhenatesCHEMONTID:0001070Inorganic non-metallic compounds containing a perrhenate as its largest oxoanion.
Non-metal pertechnetatesCHEMONTID:0001071Inorganic non-metallic compounds containing a pertechnetate as its largest oxoanion.
Non-metal phosphitesCHEMONTID:0001072Inorganic non-metallic compounds containing a phosphite as its largest oxoanion.
Non-metal phosphatesCHEMONTID:0001073Inorganic non-metallic compoundscontaining a phosphate as its largest oxoanion.
Non-metal pyrophosphatesCHEMONTID:0001074Inorganic non-metallic compoundscontaining a pyrophosphate as its largest oxoanion.
Non-metal selenatesCHEMONTID:0001075Inorganic non-metallic compoundscontaining a selenate as its largest oxoanion.
Non-metal selenitesCHEMONTID:0001076Inorganic non-metallic compoundscontaining a selenite as its largest oxoanion.
Non-metal sulfatesCHEMONTID:0001077Inorganic non-metallic compoundscontaining a sulfate as its largest oxoanion.
Non-metal sulfitesCHEMONTID:0001078Inorganic non-metallic compoundscontaining a sulfite as its largest oxoanion.
Non-metal superoxidesCHEMONTID:0001079Inorganic non-metallic compoundscontaining a superoxide as its largest oxoanion.
TetrazolinesCHEMONTID:0001080Organic compounds containing a tetrazoline ring, which is a five-member unsaturated aliphatic heterocycle made up of four nitrogen atoms, a one carbon atom, and one double bond.
Non-metal peroxomonosulfatesCHEMONTID:0001081Inorganic non-metallic compoundscontaining a peroxomonosulfate as its largest oxoanion.
Non-metal peroxodisulfatesCHEMONTID:0001082Inorganic non-metallic compoundscontaining a peroxodisulfate as its largest oxoanion.
Non-metal pyrosulfatesCHEMONTID:0001083Inorganic non-metallic compoundscontaining a pyrosulfate as its largest oxoanion.
Non-metal tetrathionatesCHEMONTID:0001084Inorganic non-metallic compoundscontaining a tetrathionate as its largest oxoanion.
Non-metal thiosulfatesCHEMONTID:0001085Inorganic non-metallic compoundscontaining a thiosulfate as its largest oxoanion.
Non-metal dithionitesCHEMONTID:0001086Inorganic non-metallic compoundscontaining a dithionite as its largest oxoanion.
Non-metal hyposulfitesCHEMONTID:0001087Inorganic non-metallic compoundscontaining a hyposulfite as its largest oxoanion.
Fatty acyl thioestersCHEMONTID:0003327Thioester derivatives of a fatty acid with the general formula RC(=O)SR', where R is the fatty acyl chain.
ToluenesCHEMONTID:0001091Compounds containing a benzene ring which bears a methane group.
BenzyloxycarbonylsCHEMONTID:0001097Organic compounds containing a carbonyl group substituted with a benzyloxyl group.
BenzofuranonesCHEMONTID:0001578Organic compounds containing a benzene ring fused to a furanone.
Flavonoid glycosidesCHEMONTID:0001111Compounds containing a carbohydrate moiety which is glycosidically linked to one of the flavonoid backbones (2-phenylchromen-4-one, 3-phenylchromen-4-one or 4-phenylcoumarin).
Alpha-keto acids and derivativesCHEMONTID:0001113Organic compounds containing an aldehyde substituted with a keto group on the adjacent carbon.
Beta-keto acids and derivativesCHEMONTID:0001114Organic compounds containing an aldehyde substituted with a keto group on the C3 carbon atom.
Gamma-keto acids and derivativesCHEMONTID:0001115Organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom.
Lipoic acids and derivativesCHEMONTID:0001116Compounds containing a lipoic acid moiety (or a derivative thereof), which consists of a pentanoic acid (or derivative) attached to the C3 carbon atom of a 1,2-dithiolane ring.
TriazolopyridinonesCHEMONTID:0001123Compounds containing triazolopyridine moiety which bears a ketone group. Triazolopyridine is a bicyclic compound consisting of a triazole fused to a pyridine ring.
Bile acids, alcohols and derivativesCHEMONTID:0001445Organic compounds containing an alcohol or acid derivative of cholic acid.
Steroid lactonesCHEMONTID:0001125Sterol lipids containing a lactone moiety linked to the steroid skeleton.
DiphenylfuransCHEMONTID:0003491Organic heterocyclic compounds that contain a furan ring substituted with a phenyl group at exactly two positions.
DiradylglycerolsCHEMONTID:0003809Glycerolipids that carry exactly two acyl chains attached to the glycerol moiety.
PhosphosphingolipidsCHEMONTID:0003392Sphingolipids with a structure based on a sphingoid base that is attached to a phosphate head group. They differ from phosphonospingolipids which have a phosphonate head group.
MonoradylglycerolsCHEMONTID:0003808Glycerolipids that carry exactly one acyl chain attached to the glycerol moiety.
ThionucleosidesCHEMONTID:0001134Nucleoside analogues that contain a thiolane or a thietane that is 1,3-disubstituted with a hydroxyl group and pyrimidine or purine base, at the 1- and 3-position, respectively.
TriradylcglycerolsCHEMONTID:0003815Glycerolipids that carry exactly three acyl chains attached to the glycerol moiety.
FlavonesCHEMONTID:0001615Flavonoids with a structure based on the backbone of 2-phenylchromen-4-one (2-phenyl-1-benzopyran-4-one).
Monocarboxylic acids and derivativesCHEMONTID:0001137Carboxylic acids containing exactly one carboxyl groups.
Glycerophosphoinositol phosphatesCHEMONTID:0002220Lipids containing a common glycerophosphate skeleton linked to at least one fatty acyl chain and an inositol-5-phosphate moiety.
ChrysenesCHEMONTID:0001142Compounds containing the polyaromatic chrysene moiety, which consists of a benzene ring fused to a phenanthrene ring system to form Benzo[a]phenanthrene.
IndolinesCHEMONTID:0001146Compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.
Organic nitro compoundsCHEMONTID:0001152Compounds having the nitro group, -NO2 (free valence on nitrogen), which may be attached to carbon, nitrogen (as in nitramines), or oxygen (as in nitrates), among other elements (in the absence of specification, C-nitro compounds are usually implied).
Organic plumbatesCHEMONTID:0001153Organic compounds containing a plumbate oxoanion, with the formula [PbO3]2-.
LipoamidesCHEMONTID:0001154Compounds containing a lipoamide moiety, which consists of a pentanamide attached to the C3 carbon atom of a 1,2-dithiolane ring.
Nitroquinolines and derivativesCHEMONTID:0001155Compounds containing a nitro group attached to a quinoline moiety.
PhenylaziridinesCHEMONTID:0001156Compounds containing a phenylaziridine moiety, which consists of an aziridine ring attached to a phenyl group.
PyrrolidonesCHEMONTID:0001158Compounds containing a pyrrolidine ring which bears a C=O group.
Ketene acetalsCHEMONTID:0001168Organic compounds comprising the ketene acetal functional group, with the general structure XC(Y)=C(R3)R4 (R1,R2=H, alkyl, aryl; X,Y=any hetero atom).
Phosphonic acid estersCHEMONTID:0001169Organic compounds containing phosphonic acid ester functional group, with the general structure ROP(=O)OH (R = organyl group).
Organosulfenic acid amidesCHEMONTID:0001172Compounds derived from a sulfenic acid, RSOH (R= organyl, not H), by replacement of -OH by -NR2.
Sulfenic acid estersCHEMONTID:0001173Compounds containing a sulfenic acid ester functional group with the general structure RSOR' (R,R'=alkyl, aryl).
Organosulfenic acid halidesCHEMONTID:0001174Compounds derived from a sulfenic acid, RSOH (R = organyl, not H), where the hydroxyl group is replace by a halogen atom.
Sulfinic acid amidesCHEMONTID:0001175Compounds derived from a sulfinic acid, RS(=O)OH (R not H), by replacement of -OH by -NR2.
Sulfinic acid estersCHEMONTID:0001176Compounds containing a sulfinic acid ester functional group with the general structure RS(=O)OR' (R,R'=alkyl, aryl).
Sulfinic acid halidesCHEMONTID:0001177Compounds derived from a sulfinic acid, RS(=O)OH (R = organyl, not H), where the hydroxyl group is replace by a halogen atom.
Organic sulfuric acidsCHEMONTID:0001180Organic compounds containing the sulfuric acid functional group, with the generic structure HOS(=O)(=O)OH.
Sulfuric acid monoamidesCHEMONTID:0001181Organic compounds containing the sulfuric acid amid functional group, with the generic structure ROS(=O)(=O)N(R')R'' (R = any atom, R' = organyl, R''=H or organyl).
CorrolesCHEMONTID:0001182Compounds containing a corrole nucleus, which contains four pyrrole rings joined in a macrocycle by three groups and one direct carbon-carbon bond linking alpha positions.
Sulfuric acid diamidesCHEMONTID:0001183Organic compounds containing the sulfuric acid diamide functional group, with the generic structure R1N(R2)S(=O)(=O)ON(R3)R4 (R1-R4 = H or organyl.
Sulfuric acid estersCHEMONTID:0003455Organic compounds containing a sulfate group that carries one or two O-ester groups.
Sulfuric acid amide estersCHEMONTID:0001186Organic compounds containing the sulfuric acid amide ester functional group, with the generic structure ROS(=O)(=O)N(R')R'' (R = organyl, R',R''=H or organyl).
ThioaldehydesCHEMONTID:0001188An organic compounds in which the oxygen of an aldehyde has been replaced by divalent sulfur, RC(=S)H. Thioaldehydes interconvert with thioketones.
Thiocarbamic acid derivativesCHEMONTID:0001368Organic compounds containing a functional group with the general structure OC(=S)NR2 or SC(=O)NR2.
Organic thiocarbonic acid derivativesCHEMONTID:0001672Organic compounds containing the thiocarbonic acid structure or a derivative thereof.
OxosteroidsCHEMONTID:0001194Steroid derivatives carrying a C=O group attached to steroid skeleton.
Thiocarboxylic acidsCHEMONTID:0001199Organic compounds containing a thiocarboxylic acid functional group, with the general structure HOC(=S)OH.
ThioestersCHEMONTID:0001200Organic compounds containing an ester of thiocarboxylic acid, with the general structure RC(=S)XR' (R=H, alkyl, aryl; R'=alkyl, aryl; X=O,S).
Organic phosphoramidesCHEMONTID:0001204Organic compounds containing the phosphoric acid amide functional group.
Carboxylic acidsCHEMONTID:0001205Compounds containing a carboxylic acid group with the formula -C(=O)OH.
Organic phosphoric acid halidesCHEMONTID:0001206Organic compounds containing the phosphoric acid halide functional group with the general structure OP(O)(=O)OX (X = halogen atom).
AlkylthiolsCHEMONTID:0001212Organic compounds containing the thiol functional group linked to an alkyl chain.
PyridoindolesCHEMONTID:0001213Compounds containing a pyridoindole, which consists of a pyridine fused to an indole. Pyridine is a 6-membered ring consisting of five carbon atoms and one nitrogen center. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
Organic thiophosphoric acidsCHEMONTID:0001219Organic compounds containing the thiophosphoric acid group ([H]OP(=S)(O[H])O[H]).
Benzyl cyanidesCHEMONTID:0001220Organic compounds containing an acetonitrile with one hydrogen replaced by a phenyl group.
Organic perrhenatesCHEMONTID:0001222Organic compounds containing the perrhenate oxoanion, with the formula [ReO4]-.
Thiocarboxylic acid amidesCHEMONTID:0001230Organic compounds containing an amide of thiocarboxylic acid, with the general structure R1C(=S)N(R2)R3 (R1-R3=H, alkyl, aryl).
Carboximidic acidsCHEMONTID:0002484Organic acids with the general formula RC(=N)-OH (R=H, organic group).
GlycerophosphoglycerophosphoglycerolsCHEMONTID:0003389Glycerophospholipids that contain three glycerol moieties sequentially linked to each other with a phosphate group. They include cardiolipins.
Organosulfenic acidsCHEMONTID:0001235Compounds containing a sulfenic acid functional group, with the general structure RSOH (R not H).
Carboxylic acid orthoestersCHEMONTID:0001237Carboxylic acid derivatives containing a carbon atom form three single bonds, each with one oxygen atom.
CaprolactonesCHEMONTID:0001241Cyclic esters of caproic acid. Caproic acid is the carboxylic acid derived from hexane with the general formula C5H11COOH.
Beta propiolactonesCHEMONTID:0001243Organic compounds containing a four-member lactone (a cyclic ester).
Delta valerolactonesCHEMONTID:0001244Cyclic organic compounds containing an oxan-2- one moiety.
Gamma butyrolactonesCHEMONTID:0001245Compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.
Metalloid plumbitesCHEMONTID:0001246Inorganic compounds in which the largest oxoanion is plumbite, and in which the heaviest atom not in an oxoanion is a metalloid.
Indolyl carboxylic acids and derivativesCHEMONTID:0001290Compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an indole ring.
GlycerophosphatesCHEMONTID:0002214Compounds containing a glycerol linked to a phosphate group.
CDP-glycerolsCHEMONTID:0001263Glycerolipids with a cytidine diphosphate attached to the oxygen O1 or O2 of the glycerol part.
PhenylacetaldehydesCHEMONTID:0001257Compounds containing a phenylacetaldehyde moiety, which consists of a phenyl group substituted at the second position by an acetalydehyde.
Organic bromatesCHEMONTID:0001259Organic compounds containing the bromate oxoanion, with the formula BrO3-.
Organic chloratesCHEMONTID:0001260Organic compounds containing the chlorate oxoanion, with the formula ClO3-.
Organic chloritesCHEMONTID:0001261Organic compounds containing the chlorite oxoanion, with the formula ClO2-.
N-sulfinylhydrazinesCHEMONTID:0001265Organonitrogen compounds with the general formula RN(R')N=S=O (R,R' = H or organyl).
Nicotinamide nucleotidesCHEMONTID:0001268Pyridine nucleotides, in which the pyridine base is nicotinamide or a derivative thereof.
Sulfinic acidsCHEMONTID:0001269Compounds containing a sulfinic acid functional group, with the general structure RS(=O)OH (R = organyl, not H).
CresolsCHEMONTID:0001272Aromatic compounds containing a methoxyphenol moiety.
Phenylpyruvic acid derivativesCHEMONTID:0001276Compounds containing a phenylpyruvic acid moiety, which consists of a phenyl group substituted at the second position by an pyruvic acid.
TetraterpenoidsCHEMONTID:0001554Terpenoid molecules containing 10 consecutively linked isoprene units.
Organic chromatesCHEMONTID:0001278Organic compounds containing the chromate oxoanion, with the formula [CrO4]2-.
Sulfur mustard compoundsCHEMONTID:0001279Compounds containing having two beta-haloalkyl groups bound to a sulfur atom.
GlycerophosphocholinesCHEMONTID:0002213Lipids containing a glycerol moiety carrying a phosphocholine at the 3-position.
Purine nucleotide sugarsCHEMONTID:0001293Purine nucleotides bound to a saccharide derivative through the terminal phosphate group.
HydroxysteroidsCHEMONTID:0001295Compounds containing an steroid backbone, with at least one hydrogen substituted by a hydroxyl group.
Pyrimidine nucleotide sugarsCHEMONTID:0001296Pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.
Nicotinic acid nucleotidesCHEMONTID:0001300Pyridine nucleotides, in which the pyridine base is nicotinic acid or a derivative thereof.
Organic phosphonic acidsCHEMONTID:0001302Organic compounds containing phosphonic acid.
Organic isocyanidesCHEMONTID:0001306Organic compounds containing the isomer HN+#C- of hydrocyanic acid, HC#N, or its hydrocarbyl derivatives RNC (RN+#C-).
Organic chromitesCHEMONTID:0001307Organic compounds containing the chromate oxoanion, with the formula Cr(O2)−.
Organophosphine oxidesCHEMONTID:0001309Organic compounds containing the phosphine oxide group, with the general formula R3P=O or R3P+O-.
Isoprenoid phosphatesCHEMONTID:0001311Prenol lipids containing a phosphate group linked to an isoprene (2-methylbuta-1,3-diene) unit.
1,2-dioxanesCHEMONTID:0001312Organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.
1,4-dioxanesCHEMONTID:0001313Organic compounds containing 1,4-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 4.
1,3-dioxanesCHEMONTID:0001314Organic compounds containing 1,3-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 3.
1,2-dioxolanesCHEMONTID:0001315Organic compounds containing 1,2-dioxolane, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 2.
1,3-dioxolanesCHEMONTID:0001316Organic compounds containing 1,3-dioxolane, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 3.
Transition metal ferratesCHEMONTID:0001317Inorganic compounds in which the largest oxoanion is ferrate, and in which the heaviest atom not in an oxoanion is a transition metal.
Pyridinecarboxylic acids and derivativesCHEMONTID:0001322Compounds containing a pyridine ring bearing a carboxylic acid group or a derivative thereof.
PyrrolizidinonesCHEMONTID:0001323Compounds containing a pyrrolizidine moiety which bears a ketone. Pyrrolizidine is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.
QuinolizidinonesCHEMONTID:0001325Compounds containing a quinolizidine moiety which bears a ketone group.
BenzoinsCHEMONTID:0001331Organic compounds containing a 1,2-hydroxy ketone attached to two phenyl groups.
IndolizidinonesCHEMONTID:0001332Polycyclic compounds containing an indolizine moiety bearing a ketone.
Fatty alcoholsCHEMONTID:0001334Aliphatic alcohols consisting of a chain of a least six carbon atoms.
1,2-diazepinesCHEMONTID:0001335Organic compounds containing 1,2-diazepine, a seven-member heterocyclic ring with two nitrogen atoms in positions 1 and 2.
1,4-diazepinesCHEMONTID:0001336Organic compounds containing 1,4-diazepine, a seven-member heterocyclic ring with two nitrogen atoms in positions 1 and 4.
1,3-diazepinesCHEMONTID:0001337Organic compounds containing 1,3-diazepine, a seven-member heterocyclic ring with two nitrogen atoms in positions 1 and 3.
1,2-oxazepinesCHEMONTID:0001338Organic compounds containing an aromatic seven-membered ring containing a nitrogen and an oxygen atom, a positions 1 and 2, respectively.
1,4-oxazepinesCHEMONTID:0001339Organic compounds containing an aromatic seven-membered wring containing a nitrogen and an oxygen atom, a positions 1 and 4, respectively.
1,3-oxazepinesCHEMONTID:0001340Organic compounds containing an aromatic seven-membered wring containing a nitrogen and an oxygen atom, a positions 1 and 3, respectively.
1,3-oxazinesCHEMONTID:0001341Organic compounds containing 1,3-oxazine, a six-member ring with a nitrogen and an oxygen atoms in ring positions 1 and 3 respectively, as well as two double bonds.
1,4-oxazinesCHEMONTID:0001342Organic compounds containing 1,4-oxazine, a six-member ring with a nitrogen and an oxygen atoms in ring positions 1 and 4 respectively, as well as two double bonds.
1,2-oxazinesCHEMONTID:0001343Organic compounds containing 1,2-oxazine, a six-member ring with a nitrogen and an oxygen atoms in ring positions 1 and 2 respectively, as well as two double bonds.
GlycerophosphoinositolsCHEMONTID:0002219Lipids containing a glycerol moiety carrying a phosphoinositol at the 3-position.
1,3-thiazinesCHEMONTID:0001347Organic compounds containing 1,3-thiazine, a six-member ring with a nitrogen and a sulfur atoms in ring positions 1 and 3 respectively, as well as two double bonds.
1,2-thiazinesCHEMONTID:0001348Organic compounds containing 1,2-thiazine, a six-member ring with a nitrogen and a sulfur atoms in ring positions 1 and 2 respectively, as well as two double bonds.
1,4-thiazinesCHEMONTID:0001349Organic compounds containing 1,4-thiazine, a six-member ring with a nitrogen and a sulfur atoms in ring positions 1 and 4 respectively, as well as two double bonds.
Meta thiazepinesCHEMONTID:0001352Aromatic compounds containing meta thiazepine moiety, which is an unsaturated seven-member heterocyclic compound, with five carbon atoms, and two sulfur atoms at position 1 and 3.
Ortho thiazepinesCHEMONTID:0001353Compounds containing a thiazepine ring, in which the sulfur and nitrogen atoms are at positions 1 and 2 respectively.
Para thiazepinesCHEMONTID:0001354Compounds containing a para thiazepine moiety, which consists of an unsaturated seven-member ring with one nitrogen atom and one sulfur at positions 1 and 4, respectively, as well as two CC double bonds.
Alpha hydroxy acids and derivativesCHEMONTID:0001359Organic compounds containing a carboxylic acid substituted with a hydroxyl group on the adjacent carbon.
Organic hydroxidesCHEMONTID:0001364Organic compounds comprising the hydroxide functional group, with the general formula OH-.
Alkaline earth metal chromitesCHEMONTID:0001365Inorganic compounds in which the largest oxoanion is chromite, and in which the heaviest atom not in an oxoanion is a alkaline earth metal.
GlycerophosphoserinesCHEMONTID:0002218Lipids containing a glycerol moiety carrying a phosphoserine at the 3-position.
Boronic acid estersCHEMONTID:0001369Compounds comprising the boronic acid ester functional group RN(X)OR' (R,R'=alkyl, aryl; X= any O, N, Hal residue).
Benzo-p-dioxinsCHEMONTID:0001379Organic compounds containing a benzene ring fused to a 1,4-dioxin ring.
Benzo-o-dioxinsCHEMONTID:0001382Organic compounds containing a benzene ring fused to a 1,2-dioxin ring.
Benzo-m-dioxinsCHEMONTID:0001383Organic compounds containing a benzene ring fused to a 1,3-dioxin ring.
Ortho dioxinsCHEMONTID:0001385Compounds containing a dioxin ring, in which the two oxygen atoms are at positions 1 and 2 respectively.
Para dioxinsCHEMONTID:0001386Compounds containing a para dioxin moiety, which consists of an unsaturated six-member ring with two oxygen atoms at positions 1 and 4, as well as two CC double bonds.
GlycosphingolipidsCHEMONTID:0003258Sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.g. S-,C-, or N-type) has been reported.
NeoflavonesCHEMONTID:0001389Neoflavonoids with a structure based on the 4-phenylcoumarin skeleton.
GlycerophosphoethanolaminesCHEMONTID:0002215Glycerolipids characterized by an ethanolamine ester of glycerophosphoric acid.
Non-metal bisulfitesCHEMONTID:0001398Inorganic non-metallic compounds containing a bisulfite as its largest oxoanion.
Ergostane steroidsCHEMONTID:0003567Steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.
1-phosphoribosyl-imidazolesCHEMONTID:0001412Organic compounds containing the imidazole ring linked to a ribose phosphate through a 1-2 bond.
Medium-chain keto acids and derivativesCHEMONTID:0001415Keto acids with a 6 to 12 carbon atoms long side chain.
Short-chain keto acids and derivativesCHEMONTID:0001416Keto acids with an alkyl chain the contains less than 6 carbon atoms.
1-ribosyl-imidazolecarboxamidesCHEMONTID:0001420Organic compounds containing the imidazole ring linked to a ribose ring through a 1-2 bond.
CeramidesCHEMONTID:0001418Lipid molecules containing a sphingosine in which the amine group is linked to a fatty acid.
Lysosphingomyelins and lysoglycosphingolipidsCHEMONTID:0001424Lipids containing either the sphingosine-phosphocholine, or the sphinganine-phosphocholine core structure.
Glycero-3-pyrophosphatesCHEMONTID:0003807Lipids structurally characterized by the presence of a glycerol moiety bonded to one or two chains, and to a pyrophosphate group at the O3-position.
Betacyanins and derivativesCHEMONTID:0001434Organic compounds containing a glycoside of indolium-2-carboxylic acid attached, with the nitrogen ring of the indolium ring attached to an ethylpyridine-2,6-dicarboxylic acid derivative. Betacyanins are red nitrogenous pigments found in certain plants, such as beetroots.
BenzoxazinonesCHEMONTID:0001437Organic compounds containing a benzene fused to an oxazine ring (a six-member aliphatic ring with four carbon atoms, one oxygen atom, and one nitrogen atom) bearing a ketone group.
Organic hypobromitesCHEMONTID:0001444Organic compounds containing the hypobromite oxoanion, with the formula BrO-.
Furoic acid and derivativesCHEMONTID:0004758Aromatic heterocyclic compounds containing a furan ring, which carries a carboxyl group or a derivative thereof.
GlycosylglycerophospholipidsCHEMONTID:0001459Glycerolipids structurally characterized by the presence of one or more sugar residues attached to the glycerol moiety of a glycerophosphate via a glycosidic linkage.
Vitamin D and derivativesCHEMONTID:0001460Compounds containing a secosteroid backbone, usually secoergostane or secocholestane.
Fatty acyl glycosidesCHEMONTID:0001766Compounds containing fatty acyl chain linked to a carbohydrate moiety through a glycosidic bond. Fatty acyl glycosides are composed of a glycosyl moiety (one or several units) linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
4-hydroxy-2-alkylquinolinesCHEMONTID:0001464Organic compounds containing a quinoline moiety with a hydroxyl group attached to the C4 atom, and an alkyl chain attached to the C2 atom.
Estrane steroidsCHEMONTID:0001466Steroids with a structure based on the estrane skeleton.
Androstane steroidsCHEMONTID:0003568Steroids with a structure based on the 19-carbon androstane skeleton.
Pregnane steroidsCHEMONTID:0003569Steroids with a structure based on the 21-carbon pregnane skeleton.
Cholestane steroidsCHEMONTID:0003566Steroids with a structure containing the 27-carbon cholestane skeleton.
Steroid estersCHEMONTID:0001691Compounds containing a steroid moiety which bears a carboxylic acid ester group.
Cyclic purine nucleotidesCHEMONTID:0001491Purine nucleotides where one ribose group of the hydroxyl moiety and one phosphate group form a ring.
Cyclic pyrimidine nucleotidesCHEMONTID:0001492Pyrimidine nucleotides where one ribose group of the hydroxyl moiety and one phosphate group form a ring.
Other glycerolipidsCHEMONTID:0001512Glycerolipids that do not belong to either the class Alk(en)yl Diacylglycerols, Diacylglycerols, Glycosylglycerols, Monoacylglycerols, Other Glycerolipids or Triacylglycerols.
Quinoline-3-sulfonamidesCHEMONTID:0001513Quinolines in which the quinoline ring system is substituted by one sulfonamide group at the 3-position.
Acyl astatidesCHEMONTID:0001519Organic compounds containing the functional group -CO-As.
Organic nitrosonium compoundsCHEMONTID:0001520Organic compounds containing the nitrosonium cation, with the general formula NO+.
Organic carbonic acidsCHEMONTID:0001521Compounds comprising the carbonic acid functional group.
AcyltrehalosesCHEMONTID:0001522Lipids containing a trehalose molecule linked to at least one fatty acid through an ester bond.
Organotin compoundsCHEMONTID:0001524Compounds containing bond between a carbon atom and a tin atom.
Organic hypochloritesCHEMONTID:0001526Organic compounds containing the hypochlorite oxoanion, with the formula ClO-.
DiphenylacetonitrilesCHEMONTID:0001527Cyclic aromatic compounds containing a diphenylacetonitrile moiety, which consists of a diphenylmethane linked to and acetonitrile to form 2,2-diphenylacetonitrile.
Organoaluminium compoundsCHEMONTID:0001529Compounds containing bond between a carbon atom and an aluminum atom.
BenzonitrilesCHEMONTID:0001530Organic compounds containing a benzene bearing a nitrile substituent.
Quinone and hydroquinone lipidsCHEMONTID:0001534Lipids structurally characterized by the presence of a quinone or hydroquinone moiety.
DifurocoumarinsCHEMONTID:0001536Polycyclic aromatic compounds containing difurocoumarin moiety consisting of a system of two fused furan rings, which is linked to the benzene ring of a coumarin.
Alpha-halocarboxylic acids and derivativesCHEMONTID:0001548Carboxylic acids (or derivative thereof) containing a halogen atom bonded to the alpha carbon atom.
SesterterpenoidsCHEMONTID:0001552Terpenes composed of five consecutive isoprene units.
EnynesCHEMONTID:0001566Hydrocarbons containing an alkene and an alkyne group.
Organophosphorotrithioic acids and derivativesCHEMONTID:0001570Organic compounds containing the organophosphorotrithioic acid structure or a derivative thereof. They have the general structure ROP(=S)(SR')SR\", where R-R\"= any atom.
Organic thiophosphoric acid amidesCHEMONTID:0001571Organic compounds containing the thiophosphoric acid amide functional group RN(R')OP(O)(O)=S, R,R'=H, alkyl, or aryl group.
Thiophosphoric acid estersCHEMONTID:0001572Organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where at least one R-group is an organyl group.
Organic thiophosphoric acid halidesCHEMONTID:0001573Organic compounds containing the thiophosphoric acid halide functional group, with the general structure RP(R')(X)=S, where R,R',R'' = O,N and X = halogen group.
Organic phosphoric acidsCHEMONTID:0001574Organic compounds containing phosphoric acid, with the general structure OP(O)(=O)O.
RetinoidsCHEMONTID:0001606Oxygenated derivatives of 3,7-dimethyl-1-(2,6,6-trimethylcyclohex-1-enyl)nona-1,3,5,7-tetraene and derivatives thereof.
Organic hyponitritesCHEMONTID:0001577Organic compounds containing the hyponitrite oxoanion, with the formula ([ON=NO]2-.
PiperidinonesCHEMONTID:0001581Compounds containing a piperidine ring which bears a ketone.
Biflavonoids and polyflavonoidsCHEMONTID:0001586Organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.
Organic hypophosphitesCHEMONTID:0001589Organic compounds containing the hypophosphite oxoanion, with the formula PO2−.
Organic iodatesCHEMONTID:0001590Organic compounds containing the iodate oxoanion, with the formula IO3-.
Inorganic sulfuryl bromidesCHEMONTID:0001591Inorganic compounds containing the sulfuryl bromide functional group, with the general structure BrS(R)(=O)=O (R=hetero atom).
PterofuransCHEMONTID:0001592Compounds containing a 3-hydroxy-2,4-dimethoxyphenyl linked to the C2 atom of a benzofuran moiety.
BilirubinsCHEMONTID:0001593Organic compounds containing a dicarboxylic acyclic tetrapyrrole derivative.
M-quinodimethanesCHEMONTID:0001602Organic compounds containing a benzene ring conjugated to two methylidene groups at carbon atoms 1 and 3, respectively.
Tetrahydrofuran lignansCHEMONTID:0001604Lignans with a structure that contains a tetrahydrofuran ring that arises from the joining of the two phenylpropanoid units.
RotenoidsCHEMONTID:0001607Phenolic compounds containing a cis-fused tetrahydrochromeno[3,4-b]chromene nucleus. Many rotenoids contain an additional ring, e.g. rotenone. They are isoflavonoids characterized by the presence of an extra carbon atom in an additional heterocyclic ring.
FuranoisoflavonoidsCHEMONTID:0002617Isoflavonoids possessing a furan ring fused to the phenyl group of the isoflavonoid skeleton.
Carbonic acid diestersCHEMONTID:0001611Compounds comprising the carbonic acid diester functional group.
IsoflavansCHEMONTID:0001612Polycyclic compounds with a structure based on the 3-phenyl-3,4-dihydro-2H-1-benzopyran skeleton.
Transition metal nitritesCHEMONTID:0001616Inorganic compounds in which the largest oxoanion is nitrite, and in which the heaviest atom not in an oxoanion is a transition metal.
Pyrimidine ribonucleotidesCHEMONTID:0002147Nucleotides consisting of a pyrimidine base linked to a ribose to which at least phosphate group is attached.
Dibenzylbutanediol lignansCHEMONTID:0001624Lignan compounds containing a 2,3-dibenzylbutane-1,4-diol moiety.
1-aryltetralin lactonesCHEMONTID:0001625Lignans with a structure containing the 1-aryltetralin skeleton, where the C9 and C9' atoms are joined to an oxygen atom to form a cyclopentanone.
Chalcones and dihydrochalconesCHEMONTID:0001630Organic compounds containing 1,3-Diphenylpropenone (benzylideneacetophenone), ArCH=CH(=O)Ar, or its derivatives formed by substitution.
HomoisoflavonesCHEMONTID:0001633Homoisoflavonoids with a structure based on the chromone system. Chromone is a bicyclic compound consisting of a 1-benzopyran, which bears a ketone group at the 4-position.
Inorganic sulfuryl chloridesCHEMONTID:0001636Inorganic compounds containing the sulfuryl chloride functional group, with the general structure ClS(R)(=O)=O (R=hetero atom).
NaphthopyranonesCHEMONTID:0001641Compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.
Inorganic sulfuryl fluoridesCHEMONTID:0001642Inorganic compounds containing the sulfuryl fluoride functional group, with the general structure FS(R)(=O)=O (R=hetero atom).
Carbonic acid ester halidesCHEMONTID:0001652Compounds comprising the carbonic acid ester halide functional group.
Carbonic acid monoestersCHEMONTID:0001655Compounds comprising the carbonic acid monoester functional group.
EnolatesCHEMONTID:0001665Deprotonated anions of enols. They have diverse forms with either of the general structure [R1]C([R2])=C([R3])[O-], RC([CH2-])=O, or R1C(R1)=COM (M=metal).
Carboxylic acid amide acetalsCHEMONTID:0001667Carboxylic acid derivatives two hydroxyl groups attached to a carbon atom, which in turn is linked to a nitrogen atom(substituted or not).
Organic diazonium saltsCHEMONTID:0001668Organic compounds comprising the diazonium functional group, with the general structure R-N=N+.
Physalins and derivativesCHEMONTID:0001671Steroidal constituents of Physalis plants which possess an unusual 13,14-seco-16,24-cyclo-steroidal ring skeleton (where the bond that is normally present between the 13 and 14 positions in other steroids is broken while a new bond between positions 16 and 24 is formed).
TropolonesCHEMONTID:0001674Compounds containing tropone ring with a hydroxyl group at ring position 2.
CucurbitacinsCHEMONTID:0001686Polycyclic compounds containing the tetracyclic cucurbitane nucleus skeleton, 19-(10->9b)-abeo-10alanost-5-ene (also known as 9b-methyl-19-nor lanosta-5-ene), with a variety of oxygenation functionalities at different positions.
Polysaccharide phosphatesCHEMONTID:0001690Carbohydrates containing more than 10 sugar units, one of which bear one or more phosphate groups.
Sulfated steroidsCHEMONTID:0001692Sterol lipids containing a sulfate group attached to the steroid skeleton.
AminotriazinesCHEMONTID:0001693Organic compounds containing an amino group attached to a triazine ring.
Spirostanes and derivativesCHEMONTID:0001700Steroidal alkaloids with a structure containing a spirostane skeleton. Spirostanes are 16b,22:22,26-diepoxycholestanes, or 22,26-epoxyfurostans. The sixth ring so formed is known as ring F. Chemically, the spiro centre at C-22 has the character of an internal acetal derived from a 16b, 26-dihydroxycholestan-22-one.
Furostanes and derivativesCHEMONTID:0001701Compounds containing or derived from the steroid parent furostane, which is a 16b,22-epoxycholestane derivative, the extra ring being labeled as\nring E.
Furospirostanes and derivativesCHEMONTID:0001702Heterocyclic steroids containing a furospirostane moiety, which a skeleton characterized by the presence of a 1,6-dioxaspiro[4.4]nonane ring system and an androstane moiety.
Hydrolyzable tanninsCHEMONTID:0001710Tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.
PhlorotanninsCHEMONTID:0001711Tannins which is formed by oligomerization of phloroglucinol. Phloroglucinol is an aromatic compound, which consists of a benzene ring bearing one hydroxyl group at the 1-,3-, and 5-positions.
Complex tanninsCHEMONTID:0001712Tannins made of a catechin bound to a gallotannin or elagitannin.
Beta hydroxy acids and derivativesCHEMONTID:0001713Compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.
HydroquinolinesCHEMONTID:0001715Derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.
Oxaborine derivativesCHEMONTID:0001717Compounds containing a six-member aliphatic heterocycle made up of one oxygen atom, a boron atom, and three carbon atoms.
PhosphoglycosphingolipidsCHEMONTID:0001721Sphingolipids containing a carbohydrate linked to the sphingoid base (sphingosine, sphinganine) through a phosphate group.
Fatty alcohol estersCHEMONTID:0001722Ester derivatives of a fatty alcohol.
PyrroloindolesCHEMONTID:0001733Compounds containing a pyrroloindole moiety, which is a tricyclic heterocycle which consists of a pyrrole ring fused to an indole. Pyrrole is 5-membered ring consisting of four carbon atoms and one nitrogen atom. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
Organic antimonatesCHEMONTID:0001740Organic compounds containing the antimonate oxoanion, with the formula Sb(OH)6-.
CoumaronochromonesCHEMONTID:0001742Polycyclic aromatic compounds containing a 1-benzopyran-4-one and a benzofuran, where the furan ring and the pyran ring are fused together.
Coumarin glycosidesCHEMONTID:0001743Aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.
Lysobisphosphatidic acidsCHEMONTID:0001749Lipids with a structure based on a bis(monoacylglycero)phosphate skeleton.
Semilysobisphosphatidic acidsCHEMONTID:0001750Bisphosphatidic acid analogues with three moles of fatty acid per mole of lipid.
Bisphosphatidic acidsCHEMONTID:0001751Organic compounds containing two 1,2-diacylglycerol moieties linked to the O1 and O4 oxygen atoms of a phosphate group.
BenzoylindolesCHEMONTID:0001753Organic compounds containing an indole attached to a benzoyl moiety through the acyl group.
DalbergionesCHEMONTID:0001758Quinone derivatives containing a dalbergione moiety, which consists of a 1-4 quinone conjugated to a phenyl group at ring carbon 2.
Pyridinium derivativesCHEMONTID:0001764Compounds containing a pyridinium ring, which is the cationic form of pyridine.
O-quinodimethanesCHEMONTID:0001778Compounds containing a benzene ring conjugated to two methylidene groups at carbon atoms 1 and 2, respectively.
DihydrofuranoquinolinesCHEMONTID:0001780Organic heterocyclic compounds with a structure based on the dihydrofuranoquinoline skeleton.
ZearalenonesCHEMONTID:0001788Macrolides which contains a fourteen-member lactone fused to 1,3-dihydroxybenzene.
FumonisinsCHEMONTID:0001792Diesters of propane-1,2,3-tricarboxylic acid (TCA) and similar long-chain aminopolyol backbones (for FB1: 2S-amino-12S,16R-dimethyl-3S,5R,10R,14S,15R-pentahydroxyeicosane). Structurally, fumonisins resemble the sphingoid bases sphinganine (SA) and sphingosine (SO) to which TCA groups have been added at the C-14 and C-15 positions.
Sparteine, lupanine, and related alkaloidsCHEMONTID:0001795Alkaloids with a structure based on either sparteine, lupanine, or derivatives thereof. These are tetracyclic compounds made of two fused quinolizidine ring systems.
Pectenotoxins and derivativesCHEMONTID:0001803A group of poly-ether-lactone toxins.
Organic pyrophosphatesCHEMONTID:0001804Organic compounds containing the pyrophosphate oxoanion, with the structure OP([O-])(=O)OP(O)([O-])=O.
QuinuclidonesCHEMONTID:0001805Compounds containing a quinuclidine moiety which bears a ketone group.
Organic arsenatesCHEMONTID:0001806Organic compounds containing the arsenate oxoanion, with the formula AsO43-.
Phenylphosphines and derivativesCHEMONTID:0001814Compounds containing a phenylphosphine, which consists of phosphine substituent bound to a phenyl group.
IsoindolinesCHEMONTID:0002496Heterocyclic compounds containing a 2,3-dihydro-1H-iso-indole moiety.
OxadiazolesCHEMONTID:0001822Organic compounds containing an oxadiazole ring, which is a five-member aromatic heterocycle with two nitrogen atoms, an oxygen atom, and a carbon atom.
HopanoidsCHEMONTID:0001823Terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).
PolyterpenoidsCHEMONTID:0001825Terpenoids consisting of more than eight isoprene units.
TerphenylsCHEMONTID:0002042Polycyclic aromatic compounds containing a terphenyl skeleton, which consists of a benzene ring substituted with two phenyl groups. Isomers of terphenyl include m-terphenyls (1,3-diphenylbenzenes), o-terphenyls (1,2-diphenylbenzenes), p-terphenyls (1,4-diphenylbenzenes).
Inorganic sulfuryl iodidesCHEMONTID:0001830Inorganic compounds containing the sulfuryl fluoride functional group, with the general structure IS(R)(=O)=O (R=hetero atom).
Thiocarbonyl s-imidesCHEMONTID:0001832Organic compounds containing a functional group with the general formula R1(R2)C=S-NR3 (R1,R3=alkyl, aryl; R2=H, alkyl, aryl).
Pyrrolizidine oximesCHEMONTID:0001835Compounds containing a pyrrolizidine moiety which bears an oxime group at ring position 1. Pyrrolizidine is a bicyclic ring system made up of two fused pyrrolidine ring sharing a nitrogen atom.
Organic peroxynitratesCHEMONTID:0001837Organic compounds containing the peroxynitrate oxoanion, with the formula [NO4]−.
Organic peroxynitritesCHEMONTID:0001838Organic compounds containing the peroxonitrite oxoanion, with the formula ONOO-.
Organic aluminatesCHEMONTID:0001839Organic compounds containing an aluminate oxoanion, with the formula [AlO2]-.
Organic stannatesCHEMONTID:0001840Organic compounds containing a stannate oxoanion, with the formula [SnO3]2-.
Organic orthovanadatesCHEMONTID:0001841Organic compounds containing the orthovanadate oxoanion, with the formula [VO4]3-.
TetrazolidinesCHEMONTID:0001842Organic compounds containing a tetrazolidine ring, which is a five-member saturated aliphatic heterocycle made up of four nitrogen atoms and a one carbon atom.
DiphenylethersCHEMONTID:0004155Aromatic compounds containing two benzene rings linked to each other through an ether group.
PhenoxazinesCHEMONTID:0001855Polycyclic aromatic compounds containing a phenoxazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a 1,4-oxazine ring.
NaphthyridinesCHEMONTID:0001857Compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.
Pyridopyrimidine carboxylic acids and derivativesCHEMONTID:0001860Pyridopyrimidines with a structure that contains pyrimidine moiety bearing a carboxylic acid group, and a pyridine ring fused to the pyrimidine.
PyridinesulfonamidesCHEMONTID:0001861Heterocyclic compounds containing a pyridine ring substituted by one or more sulfonamide groups.
Oxirane carboxylic acids and derivativesCHEMONTID:0001864Compounds containing an oxirane ring bearing a carboxylic acid group (or a derivative thereof).
NaphthohydroquinonesCHEMONTID:0001870Compounds containing a naphthohydroquinone moiety, which consists of a benzene ring fused to a bezene-1,4-diol (hydroquinone).
Naphthalenecarboxylic acids and derivativesCHEMONTID:0001871Compounds containing a naphthalene moiety, which bears a carboxylic acid group or a derivative at one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
P-quinodimethanesCHEMONTID:0001872Compounds containing a benzene ring conjugated to two methylidene groups at carbon atoms 1 and 4, respectively..
IsobenzofuranonesCHEMONTID:0003409Compounds containing a 2-benzofuran moiety that carries an oxo group at the 1 position.
SulfonphthalidesCHEMONTID:0001874Compounds containing a sulfonphthalide moiety, which consists of a benzene ring fused to an oxathiole-1,1-dione.
Azetidinecarboxylic acids or derivativesCHEMONTID:0001876Organic compounds containing a carboxylic acid group (or a derivative thereof) attached to an azetidine ring.
Aziridinecarboxylic acids or derivativesCHEMONTID:0001877Organic compounds containing a carboxylic acid group(or a derivative thereof) attached to an aziridine ring.
Beta sultamsCHEMONTID:0001882Organic compounds containing a sulfonamide group in which the N-S bond is part of a four member ring.
Delta sultamsCHEMONTID:0001885Cyclic organic compounds containing a 1,2-thiazinane-1,1-dione moiety.
Beta sultonesCHEMONTID:0001887Organic compounds containing a four-member cyclic ester of hydroxy sulfonic acid, analogous to lactones. Here, the O-S bond is part of the ring.
Gamma sultonesCHEMONTID:0001888Organic compounds containing a gamma-sultone, a Intramolecular cyclic ester of hydroxy sulfonic acid, with a SO ring bond, and three ring carbon atoms.
SulfinylbenzimidazolesCHEMONTID:0001891Polycyclic aromatic compounds containing a sulfinyl group attached at the position 2 of a benzimidazole moiety.
Organic triazenesCHEMONTID:0001898Organic compounds containing the triazene group (-N-N=N), which consists of an amine directly bonding to an azo group.
CylindrospermopsinsCHEMONTID:0001899Compounds containing a cylindrospermopsin moiety, which contains a triazaacenaphthylene moiety linked to a pyrimidinedione.
Pyrrolidine carboxylic acids and derivativesCHEMONTID:0001903Compounds containing a pyrrolidine ring which bears a carboxylic acid or a derivative thereof. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
SulfinylaminesCHEMONTID:0001905Compounds containing the sulfinylamine functional group, with the general structure RN=S=O.
PhenanthroindolizidinesCHEMONTID:0001906Aromatic polycyclic compounds containing the phenanthroindolizidine skeleton, which is structurally characterized by an indolizidine and a phenanthrene, where the indolizidine is fused to the second benzene ring of a phenanthrene.
PhenanthroquinolizidinesCHEMONTID:0001907Aromatic polycyclic compounds containing the phenanthroindolizidine skeleton, which is structurally characterized by an indolizidine and a phenanthrene, where the quinolizidine is fused to the second benzene ring of a phenanthrene.
Anthracenecarboxylic acids and derivativesCHEMONTID:0001911Organic compounds containing a carboxylic acid group (or a derivative thereof) attached to an anthracene ring system.
PyridoisoindolesCHEMONTID:0001912Compounds containing a pyridoisoindole, which consists of a pyridine fused to an isoindole.
ThiazinanethionesCHEMONTID:0001919Heterocyclic compounds containing a thioketone group conjugated to a saturated six-member ring with four carbon atoms, one sulfur atom, and one nitrogen.
TriazinonesCHEMONTID:0001920Compounds containing a triazine ring which bears a ketone group a carbon atom.
TriazinethionesCHEMONTID:0001922Compounds containing a triazine ring which bears a thioketone group.
OxatriazolesCHEMONTID:0001931Compounds containing an oxatriazole moiety, which consists of an unsaturated aliphatic five-member ring with one oxygen atom, three nitrogen, one carbon atom, and two double bonds. Isomers of oxatriazole include 1,2,3,4-oxatriazole, and 1,2,3,5-oxatriazole.
OxatriazolidinesCHEMONTID:0001932Organic compounds containing an oxatriazolidine ring, which is a five-member saturated aliphatic heterocycle with three nitrogen atoms, an oxygen atom, and a carbon atom.
OxadiazolidinesCHEMONTID:0001933Organic compounds containing an oxadiazole ring, which is a five-member saturated aliphatic heterocycle with two nitrogen atoms, an oxygen atom, and two carbon atoms.
N-phenylureasCHEMONTID:0001935Compounds containing a N-phenylurea moiety, which is structurally characterized by a phenyl group linked to one nitrogen atom of a urea group.
AminothiophenesCHEMONTID:0001936Organic compounds containing an amino group attached to a thiophene ring.
PyridoxinesCHEMONTID:0001948Pyridoxal derivatives in which the carbaldehyde group at position 2 of the pyridoxal moiety is replaced by a hydroxymethyl group.
PyridoxaminesCHEMONTID:0001966Pyridoxal derivatives in which the carbaldehyde moiety is substituted at position 2 by an amine.
Furan lignansCHEMONTID:0001970Lignans with a structure based on 3,4-dibenzyloxolane or a (4-benzyl-2-phenyloxolan-3-yl)methanol skeleton.
Furofuran lignansCHEMONTID:0001971Lignans with a structure based on 1,4-diphenyl-hexahydrofuro[3,4-c]furan skeleton.
BenzoxazolonesCHEMONTID:0001973Organic compounds containing a benzene fused to an oxazole ring (a five-member aliphatic ring with three carbon atoms, one oxygen atom, and one nitrogen atom) bearing a ketone group.
Piperidinecarboxylic acids and derivativesCHEMONTID:0001974Compounds containing a piperidine ring which bears a carboxylic acid group (or a derivative thereof).
PyrrolidinylpyridinesCHEMONTID:0001975Compounds containing a pyrrolidinylpyridine ring system, which consists of a pyrrolidine ring linked to a pyridine ring.
FuranonesCHEMONTID:0001982Compounds containing a furan ring bearing a ketone group.
Tricarboxylic acids and derivativesCHEMONTID:0001986Carboxylic acids containing exactly three carboxyl groups.
IsosorbidesCHEMONTID:0001987Organic polycyclic compounds containing an isosorbide(1,4-Dianhydrosorbitol) moiety, which consists of two -oxolan-3-ol rings.
DibenzoxepinesCHEMONTID:0001988Compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring.
Pyran carboxylic acids and derivativesCHEMONTID:0001991Compounds containing a pyran ring which bears a carboxylic acid group (or a derivative thereof).
PyrazolylpyridinesCHEMONTID:0002006Compounds containing a pyrazolylpyridine skeleton, which consists of a pyrazole linked (not fused) to a pyridine by a bond.
Indolecarboxylic acids and derivativesCHEMONTID:0002013Compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole.
ThiadiazolidinesCHEMONTID:0002015Cyclic organic compounds containing a thiadiazole ring, which is a five-member saturated aliphatic heterocycle made up of one sulfur atom and two nitrogen atoms.
ThiadiazolinesCHEMONTID:0002016Cyclic organic compounds containing a thiadiazoline ring, which is a five-member unsaturated aliphatic heterocycle made up of one sulfur atom and two nitrogen atoms.
Thiophene carboxylic acids and derivativesCHEMONTID:0002017Compounds containing a thiophene ring which bears a carboxylic acid group (or a salt/ester thereof).
DithiohemiacetalsCHEMONTID:0002026Compounds containing a dithiohemiacetal group with the general formula R2C(SR')SH, where R' != H.
Substituted pyrrolesCHEMONTID:0002257Heterocyclic compounds containing a pyrrole ring substituted at one or more positions.
Lysergic acids and derivativesCHEMONTID:0002680Alkaloids with a structure based on the lysergic acid skeleton.
Stigmastanes and derivativesCHEMONTID:0002031Sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24.
Organoselenium compoundsCHEMONTID:0002468Organic compounds containing a carbon-selenium bond.
Oxonium ylidesCHEMONTID:0003701Compounds having the general structure R2[O+]-C-R2. Oxonium ylides also constituted a class of 1,3-dipolar compounds of general structure R2C=[O+]-Y- , comprising carbonyl imides, carbonyl oxides and carbonyl ylides.
Azo imidesCHEMONTID:0002036N-Imides of azo compounds, analogous to azoxy compounds, having a delocalized structure.
Azoxy compoundsCHEMONTID:0002037Organic compounds sharing a common functional group with the general structure RN=N+(O-)R.
Gorgostanes and derivativesCHEMONTID:0002039Steroids containing a gorgostane moiety, which a skeleton characterized by the presence.
Acenaphthenes and derivativesCHEMONTID:0002043Organic compounds containing a naphthalene ring with an ethylene bridge connecting positions 1 and 8.
PhenylnaphthalenesCHEMONTID:0002044Compounds containing a phenylnaphthalene skeleton, which consists of a naphthalene bound to a phenyl group.
Organosilicon compoundsCHEMONTID:0003194Organic compounds containing a C[Si] bond.
Isoquinolones and derivativesCHEMONTID:0002054Aromatic polycyclic compounds containing a ketone bearing isoquinoline moiety.
PhenoxathiinsCHEMONTID:0002060Polycyclic aromatic compounds containing a phenoxathiin moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a 1,4-oxathiin ring.
Organic orthonitratesCHEMONTID:0002065Organic compounds containing the orhthonitrate oxoanion, with the formula [NO4]3−.
Organic perbromatesCHEMONTID:0002066Organic compounds containing the perbromate oxoanion, with the formula [BrO4]-.
Organic perchloratesCHEMONTID:0002067Organic compounds containing the perchlorate oxoanion, with the formula [ClO4]-.
Organic periodatesCHEMONTID:0002068Organic compounds containing the periodate oxoanion, with the formula [IO4]-.
Organic permanganatesCHEMONTID:0002069Organic compounds containing the permanganate oxoanion, with the formula [MnO4]-.
Organic pertechnetatesCHEMONTID:0002070Organic compounds containing the pertechnetate oxoanion, with the formula [TcO4]-.
Organic phosphitesCHEMONTID:0002071Organic compounds containing the phosphite oxoanion, with the formula [PO3]3-.
Organic selenatesCHEMONTID:0002072Organic compounds containing the selenate oxoanion, with the formula [SeO4]2-.
Organic selenitesCHEMONTID:0002073Organic compounds containing the selenite oxoanion, with the formula [SeO3]2-.
Organic sulfitesCHEMONTID:0004456Organic compounds containing the selenite oxoanion, with the formula [SO3]2-, or its conjugated base.
Organic peroxomonosulfatesCHEMONTID:0002076Organic compounds containing the peroxomonosulfate oxoanion, with the formula [SO5]2-.
Organic peroxodisulfatesCHEMONTID:0002077Organic compounds containing the peroxodisulfate oxoanion, with the formula [S2O8]2−.
Organic pyrosulfatesCHEMONTID:0002078Organic compounds containing the pyrosulfate oxoanion, with the structure OS([O-])(=O)OS(O)([O-])=O.
Organic tetrathionatesCHEMONTID:0002079Organic compounds containing the tetrathionate oxoanion, with the formula [S4O6]2−.
Organic thiosulfatesCHEMONTID:0002080Organic compounds containing the thiosulfate oxoanion, with the formula [S2O3]2-, or its conjugate base.
Organic dithionitesCHEMONTID:0002081Organic compounds containing the dithionite oxoanion, with the formula [S2O4]2−.
Organic hyposulfitesCHEMONTID:0002082Organic compounds containing the hyposulfite oxoanion, with the formula [SO2]2-.
IsoxazolidinesCHEMONTID:0002083Organic heterocyclic compounds containing an isoxazolidine moiety, with a structure characterized by a five-member saturated aliphatic ring with one oxygen atom and one nitrogen atom at ring positions 1 and 2, respectively.
Beta sultimsCHEMONTID:0002096Organic compounds containing a sulfonamide group in which the N=S double bond is part of a four member ring. Beta Sultims are tautomeric forms of sultams, where N-S bond is double and not single.
Gamma sultimsCHEMONTID:0002097Organic compounds containing a sulfonamide group in which the N=S double bond is part of a five member ring. Gamma Sultims are tautomeric forms of gamma sultams, where N-S bond is double and not single.
Delta sultimsCHEMONTID:0002098Organic compounds containing a sulfonamide group in which the N=S double bond is part of a six member ring. Sultims are tautomeric forms of sultams, where N-S bond is double and not single.
CyclohexylphenolsCHEMONTID:0002099Compounds containing a cyclohexane lined to a phenol group.
AzarsinanesCHEMONTID:0002102Organic compounds containing a six-member saturated aliphatic ring containing a nitrogen atom (at carbon 1), an arsenic atom (at carbon 4), and four carbon atoms.
Benzarsazines and derivativesCHEMONTID:0002103Polycyclic aromatic compounds containing a benzene ring fused to a 1,4-azarsine ring.
AzaborinesCHEMONTID:0002112Organic compounds containing a six-member aromatic ring containing a nitrogen atom, an arsenic atom, and four carbon atoms.
AzaborininesCHEMONTID:0002113Organic compounds containing a six-member unsaturated aliphatic ring containing a nitrogen atom, an arsenic atom, and four carbon atoms.
MonothioacetalsCHEMONTID:0002131Compounds containing a monothioacetal functional group with the general structure R2C(OR')(SR').
DithioacetalsCHEMONTID:0002132Compounds containing a dithioacetal functional group with the general structure R2C(SR')2.
Purine deoxyribonucleotidesCHEMONTID:0002134Purine nucleotides where the purine moiety is linked to a ribose lacking a hydroxyl group at one or more positions.
Pyrimidine deoxyribonucleotidesCHEMONTID:0002148Pyrimidine nucleotides where the purine moiety is linked to a ribose lacking a hydroxyl group at one or more positions.
Purine 2'-deoxyribonucleosidesCHEMONTID:0002177Compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.
Purine 3'-deoxyribonucleosidesCHEMONTID:0002178Compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.
Purine 2',3'-dideoxyribonucleosidesCHEMONTID:0002179Compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.
Pyrimidine 2'-deoxyribonucleosidesCHEMONTID:0002180Compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.
Pyrimidine 3'-deoxyribonucleosidesCHEMONTID:0002181Compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 3.
Pyrimidine 2',3'-dideoxyribonucleosidesCHEMONTID:0002182Compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.
1-phenethyltetrahydroisoquinolinesCHEMONTID:0002189Compounds containing a phenethyl group attached to the C4-atom of a tetrahydroisoquinoline moiety.
NaphthylisoquinolinesCHEMONTID:0002195Polycyclic aromatic compounds containing a naphthalene moiety linked to an isoquinoline through a CC or CN single bond.
PhenylquinolinesCHEMONTID:0002348Heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.
PhenylazetidinesCHEMONTID:0002200Polycyclic aromatic compounds containing a phenyl ring substituted with an azetidine ring.
IsoxazolinesCHEMONTID:0002211Compounds containing a five-member unsaturated aliphatic ring, with an oxygen atom adjacent to a nitrogen atoms, and three carbon atoms.
PolyprenylphenolsCHEMONTID:0002221Compounds containing a polyisoprene chain attached to a phenol group.
Oxaborole derivativesCHEMONTID:0002227Compounds containing a five-member aliphatic heterocycle made up of one oxygen atom, a boron atom, and three carbon atoms.
AminotetrazinesCHEMONTID:0002234Compounds containing an amine group attached to a tetrazine. Tetrazine is a six-membered aromatic heterocycle made up of four nitrogen atoms and a two carbon atoms.
Delta sultonesCHEMONTID:0002236Organic compounds containing a delta-sultone, an intramolecular cyclic ester of hydroxy sulfonic acid, with a SO ring bond, and four ring carbon atoms.
Quinolizine carboxylic acids and derivativesCHEMONTID:0002238Compounds containing a carboxylic group attached to a quinolizine moiety.
Aromatic aminesCHEMONTID:0002241Aromatic compounds containing an aryl group linked to an amine.
PhenylacetylindolesCHEMONTID:0002243Compounds containing an indole moiety attached to phenylacetate derivative.
NaphthoylindolesCHEMONTID:0002247Polycyclic compounds containing an indole moiety that is N-linked to the carboxamide group attached to naphthalene.
Quinoline carboxamidesCHEMONTID:0002553Quinolines in which the quinoline ring system is substituted by one or more carboxamide groups.
Actinide selenophosphatesCHEMONTID:0002266Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is an actinide.
Alkali metal selenophosphatesCHEMONTID:0002267Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Lanthanide selenophosphatesCHEMONTID:0002268Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Metalloid selenophosphatesCHEMONTID:0002269Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is a metalloid.
Non-metal selenophosphatesCHEMONTID:0002270Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is a non-metal element.
Post-transition metal selenophosphatesCHEMONTID:0002271Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Transition metal selenophosphatesCHEMONTID:0002272Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is a transition metal.
NitronaphthalenesCHEMONTID:0002275Polycyclic aromatic compounds containing a naphthalene moiety substituted by one or more nitro groups.
Alkaline earth metal selenophosphatesCHEMONTID:0002277Inorganic compounds in which the largest oxoanion is selenophosphate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Pyrrolopyrimidinecarboxylic acids and derivativesCHEMONTID:0002284Heterocyclic aromatic compounds containing a pyrrolopyrimidine moiety substituted by one or more carboxylic acid groups.
Pyrroline carboxylic acids and derivativesCHEMONTID:0002287Heterocyclic compounds containing a pyrroline ring substituted by one or more carboxylic acid groups (or derivative thereof).
ThiomorpholinesCHEMONTID:0002288Heterocyclic compounds containing a thiomorpholine ring, which is a six-membered aliphatic ring containing one nitrogen atom and one sulfur atom at positions 1 and 4 respectively, and four carbon atoms.
Non-metal dithiophosphatesCHEMONTID:0002290Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is a non-metal element.
Non-metal thiophosphatesCHEMONTID:0002291Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is a non-metal element.
Actinide dithiophosphatesCHEMONTID:0002292Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is an actinide.
Actinide thiophosphatesCHEMONTID:0002293Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is an actinide.
Alkali metal thiophosphatesCHEMONTID:0002294Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkali metal dithiophosphatesCHEMONTID:0002295Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkaline earth metal thiophosphatesCHEMONTID:0002296Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Alkaline earth metal dithiophosphatesCHEMONTID:0002297Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Lanthanide thiophosphatesCHEMONTID:0002298Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Lanthanide dithiophosphatesCHEMONTID:0002299Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Metalloid thiophosphatesCHEMONTID:0002300Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is a metalloid.
Metalloid dithiophosphatesCHEMONTID:0002301Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is a metalloid.
Post-transition metal thiophosphatesCHEMONTID:0002302Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Post-transition metal dithiophosphatesCHEMONTID:0002303Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Transition metal thiophosphatesCHEMONTID:0002304Inorganic compounds in which the largest oxoanion is thiophosphate, and in which the heaviest atom not in an oxoanion is a transition metal.
Transition metal dithiophosphatesCHEMONTID:0002305Inorganic compounds in which the largest oxoanion is dithiophosphate, and in which the heaviest atom not in an oxoanion is a transition metal.
PhenylpyridinesCHEMONTID:0002317Polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond.
HalophenolsCHEMONTID:0002320Aromatic compounds containing benzene substituted by a hydroxyl group and a halogen atom.
Cycloartanols and derivativesCHEMONTID:0002321Steroids containing a cycloartanol moiety.
BenzisoxazolonesCHEMONTID:0002333Aromatic compounds containing a benzene ring fused to an isoxazolone moiety.
PhenylpyrrolinesCHEMONTID:0002335Polycyclic aromatic compounds containing a benzene ring linked to a pyrroline ring through a CC or CN bond.
PhenylpyrrolidinesCHEMONTID:0002336Polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
Azasteroids and derivativesCHEMONTID:0002340Steroid derivatives in which one carbon atom in the steroidal skeleton has been substituted with a nitrogen atom.
Thioenol ethersCHEMONTID:0002352Compounds containing the enol ether functional group, with the formula R3SCR2=CR1.
BenzoisochromanequinonesCHEMONTID:0002355Benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.
AminopiperidinesCHEMONTID:0002357Compounds containing a piperidine that carries an amino group.
Thiobenzoic acids and derivativesCHEMONTID:0002361Organic compounds containing thiobenzoic acid or a derivative thereof.
PhenylacetamidesCHEMONTID:0002363Amide derivatives of phenylacetic acids.
Non-metal phosphonatesCHEMONTID:0002366Inorganic non-metallic compounds containing a phosphonate as its largest oxoanion.
Actinide phosphonatesCHEMONTID:0002367Inorganic compounds in which the largest oxoanion is phosphonate, and in which the heaviest atom not in an oxoanion is an actinide.
Alkali metal phosphonatesCHEMONTID:0002368Inorganic compounds in which the largest oxoanion is phosphonate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Alkaline earth metal phosphonatesCHEMONTID:0002369Inorganic compounds in which the largest oxoanion is phosphonate, and in which the heaviest atom not in an oxoanion is an alkaline earth metal.
Lanthanide phosphonatesCHEMONTID:0002370Inorganic compounds in which the largest oxoanion is phosphonate, and in which the heaviest atom not in an oxoanion is a lanthanide.
Metalloid phosphonatesCHEMONTID:0002371Inorganic compounds in which the largest oxoanion is phosphonate, and in which the heaviest atom not in an oxoanion is a metalloid.
Post-transition metal phosphonatesCHEMONTID:0002372Inorganic compounds in which the largest oxoanion is phosphonate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Transition metal phosphonatesCHEMONTID:0002373Inorganic compounds in which the largest oxoanion phosphonate, and in which the heaviest atom not in an oxoanion is a transition metal.
FuranoquinolinesCHEMONTID:0002374Compounds containing a furan ring fused to a quinoline.
17-furanylsteroids and derivativesCHEMONTID:0002381Steroidal compounds having a furanyl group linked to the steroid backbone at the C17 position.
Oxasteroids and derivativesCHEMONTID:0002382Steroid derivatives where a carbon atom of the steroid is replaced by an oxygen atom.
Thiasteroids and derivativesCHEMONTID:0002383Steroid derivatives in which one carbon atom in the steroidal skeleton has been substituted with a sulfur atom.
Glycerol ethersCHEMONTID:0002391Lipids containing an ether derivative of glycerol.
Azomethine imidesCHEMONTID:00023961,3-dipolar N-imides of azomethines. They have the general formula R1C(R2)=[N+](R3)[N-]R4 or R1[C-](R2)[N+](R3)=[N-]R4, where R1-R4 = organyl group.
NitronesCHEMONTID:0002397N-oxides of imines, with the general structure R1C(R2)=[N+](R3)[O-] (R3 is not an Hydrogen atom).
Azomethine ylidesCHEMONTID:00023981,3-Dipolar Compounds having the general structure [C-][N+]=C(R)(R').
Azonic acids and derivativesCHEMONTID:0002399Organic acids with the general formula R[N+](OR')(OR'')O- (R = organyl; R',R\" = any atom).
Organotellurium compoundsCHEMONTID:0002469Compounds containing bond between a carbon atom and a tellurium atom.
SelenazolesCHEMONTID:0002428Compounds containing a five-membered aromatic ring with a the carbon atom replaced by a selenium atom (at position 1) and a nitrogen atom (at position 2 or 3).
Naphthols and derivativesCHEMONTID:0002441Naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.
NitrosopiperidinesCHEMONTID:0002442Piperidines with a nitroso functional group attached to the piperidine ring.
Peroxycarboxylic acids and derivativesCHEMONTID:0002445Organic acids with the general formula OOC(R)=O (R = H, organyl group).
Nitrile imidesCHEMONTID:0002461Organic compounds with the general structure RC#[N+][N-]R, R[C+]=N=[N-]R, or R[C-]=[N+]=NR.
YnolsCHEMONTID:0002465Organooxygen compounds with the general formula R#CO (R = organyl).
Perselenic acidsCHEMONTID:0002474Compounds containing a P-hydrocarbyl derivative of perselenic acid.
Telluric acidsCHEMONTID:0002481Organic acids containing a telluric acid group.
Organic nitric acidsCHEMONTID:0002487Compounds containing an organonitric acid group.
IndolesCHEMONTID:0002497Compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
AlkanesCHEMONTID:0002500Acyclic branched or unbranched hydrocarbons having the general formula CnH2n+2 , and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.
Cinnamic acidsCHEMONTID:0002504Organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid.
HomoisoflavansCHEMONTID:0002508Homoisoflavonoids with a structure based on the chromane system. Chromone is a bicyclic compound consisting of a 3,4-dihydro-1-benzopyran.
P-toluquinols and derivativesCHEMONTID:0002520Toluenes with two hydroxyl group attached to the benzene ring in a para-relationship. The hydrogen atom of either hydroxyl group can be substituted by another atom.
IsoflavanquinonesCHEMONTID:0002523Isoflavans where the phenyl group carries two C=O groups at position 1 and 4, respectively.
Cyclopropanecarboxylic acids and derivativesCHEMONTID:0002524Organic compounds containing a carboxyl group (or a derivative thereof) attached to a cyclopropane ring.
PhenoxidesCHEMONTID:0002536Salts or analogous metal derivatives of phenols.
Isothiocyanate acidsCHEMONTID:0002537Acidic derivatives of isothiocyanates with the general formula RC(=O)N=C=S.
BenzylethersCHEMONTID:0002542Aromatic ethers with the general formula ROCR' (R = alkyl, aryl; R'=benzene).
Quinoline carboxylic acidsCHEMONTID:0002552Quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.
Pyrrole carboxylic acids and derivativesCHEMONTID:0002554Heterocyclic compounds containing a pyrrole ring bearing a carboxyl group (or a derivative thereof).
Isoquinoline quinonesCHEMONTID:0002567Isoquinoline derivative with a structure containing a 5,8-dihydroisoquinoline-5,8-dione skeleton.
Quinoline quinonesCHEMONTID:0002570Quinoline derivative with a structure containing a 5,8-dihydroisoquinoline-5,8-dione skeleton.
PhenanthraquinonesCHEMONTID:0002571Phenanthrene derivatives containing two ketone groups at position C9 and C10, respectively.
NaphthothiophenesCHEMONTID:0002572Compounds containing a naphthalene (or a derivative) fused to thiophene.
ThienobenzoxepinesCHEMONTID:0002573Compounds containing a benzoxepine fused to a thiophene ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom.
1,2-oxazinanesCHEMONTID:0002576Compounds containing an oxazinane ring with the nitrogen atom and the oxygen atom at positions 1 and 2, respectively.
PhenylthiazetidinesCHEMONTID:0002579Compounds containing a thiazetidine ring conjugated to a phenyl group.
NeoflavansCHEMONTID:0002581Neoflavonoids with a structure based on a 3,4-dihydro-4-aryl-2H-1-benzopyran skeleton.
NeoflavenesCHEMONTID:0002582Neoflavonoids with a structure based on a 4-phenylchromene skeleton.
DalbergiquinolsCHEMONTID:0002583Neoflavonoids with a structure based on a 3,3-diarylprop-1-ene skeleton.
PhenylbenzofuransCHEMONTID:0002584Organic aromatic compounds that contain a phenyl group attached to a benzofuran moiety. Benzofuran is a bicyclic compound containing a benzene fused to a furan.
O-methylated flavonoidsCHEMONTID:0002585Flavonoids with methoxy groups conjugated to the flavonoid backbone.
O-methylated isoflavonoidsCHEMONTID:0002586Isoflavonoids with methoxy groups conjugated to the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
BromohydrinsCHEMONTID:0002607Alcohols substituted by a bromine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
ChlorohydrinsCHEMONTID:0002608Alcohols substituted by a chlorine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
FluorohydrinsCHEMONTID:0002609Alcohols substituted by a fluorine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
IodohydrinsCHEMONTID:0002610Alcohols substituted by a iodine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.
Furanoflavonoids and dihydrofuranoflavonoidsCHEMONTID:0002614Flavonoids possessing a furan (or dihydrofuran) ring fused to the benzopyran moiety of the flavonoid skeleton.
BenzylpiperidinesCHEMONTID:0003087Heterocyclic compounds containing a piperidine ring conjugated to a benzyl group.
ThiohydroquinonesCHEMONTID:0002623Organic compounds similar to hydroquinones wit the difference that one hydroxyl group is replaced by a thiol group.
ArylsulfatesCHEMONTID:0004258Organic compounds containing a sulfate group that carries an aryl group through an ether group.
HydroxycoumarinsCHEMONTID:0002908Coumarins that contain one or more hydroxyl groups attached to the coumarin skeleton.
Halogenated steroidsCHEMONTID:0002645Compounds containing an steroid backbone, with at least one hydrogen substituted by a halogen atom.
Cyclic diarylheptanoidsCHEMONTID:0002652Diarylheptanoids where the two aromatic rings of the skeleton are joined by a CC bond or an ether group, in addition to the heptane chain.
PhenalenonesCHEMONTID:0002654Compounds containing a phenalene ring system, which carries a keto group.
Aristolochic acids and derivativesCHEMONTID:0002664Organic heterocyclic compounds with a structure characterized by a nitrophenanthro[3,4-d][1,3]dioxole ring system substituted at position 5, 6, and 8 by a carboxyl group (or a derivative thereof), a nitro group, and a methoxy group, respectively.
Hexahydrobenzophenanthridine alkaloidsCHEMONTID:0002666Alkaloids containing a hexahydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a hexahydrophenanthridine moiety.
Dihydrobenzophenanthridine alkaloidsCHEMONTID:0002667Alkaloids containing a dihydrobenzophenanthridine skeleton, which is a tetracyclic compound containing a benzene fused to a dihydrophenanthridine moiety.
N-demethylbenzophenanthridine alkaloidsCHEMONTID:0002668Alkaloids containing a N-demethylbenzophenanthridine skeleton, which consists of a benzene ring fused to one benzene moiety of the tricyclic phenanthiridine system. These compounds do not carry a methyl group at the N-atom of the phenanthridine moiety, in contrast to other benzophenanthridine alkaloids.
Quaternary benzophenanthridine alkaloidsCHEMONTID:0002669Alkaloids containing a quaternary N-demethylbenzophenanthridine skeleton, where the nitrogen atom of the phenanthridine moiety is part of four bonds.
Secobenzophenanthridine alkaloidsCHEMONTID:0002670Alkaloids containing a secobenzophenanthridine skeleton.
BenzylaminesCHEMONTID:0002673Organic compounds containing benzylamine, which consists of a benzene group attached to an amine group.
CyclohexylaminesCHEMONTID:0002674Organic compounds containing a cyclohexylamine moiety, which consist of a cyclohexane ring attached to an amine group.
PeroxolsCHEMONTID:0002676Monosubstituted derivatives of hydrogen peroxide, with the general formula ROOH, where R is an organic group.
IndenoazepinesCHEMONTID:0002677Heterocyclic aromatic compounds with a structure based on an indene ring system fused to an azepine ring.
Benzo-1,2-dioxanesCHEMONTID:0002700Heterocyclic compounds containing a benzene ring fused to a 1,2-dioxane ring.
Benzo-1,3-dioxanesCHEMONTID:0002701Heterocyclic compounds containing a benzene ring fused to a 1,3-dioxane ring.
Benzo-1,4-dioxanesCHEMONTID:0002702Heterocyclic compounds containing a benzene ring fused to a 1,4-dioxane ring.
Benzo-2,3-dioxanesCHEMONTID:0002703Heterocyclic compounds containing a benzene ring fused to a 2,3-dioxane ring.
PhenylbenzodioxanesCHEMONTID:0002704Benzodioxanes having a phenyl group attached to the dioxane moiety.
Polyphenyl ethersCHEMONTID:0002717Polymers of unsubstituted phenoxy groups linked through ether bonds.
Polyphenyl thioethersCHEMONTID:0002718Polymers of unsubstituted phenoxy groups linked through thioether bonds.
Matrine alkaloidsCHEMONTID:0002720Lupin alkaloids with a structure based on the matrine skeleton, a four-ring skeleton that based on a saturated dipyrido[2,1-f:3',2',1'-ij][1,6]naphthyridin-10-one skeleton.
Lupinine-type alkaloidsCHEMONTID:0002721Lupin alkaloids with a structure based on the lupinine skeleton, which is a bicyclic compound consisting of a quinolizidine.
Cytisine and derivativesCHEMONTID:0002722Lupin alkaloids with a structure based on the cytisine skeleton, which is a tetracyclic ketone containing fused pyridine and piperidine rings that form pyrido[1,2a][1,5]diazocin-8-one.
Anagyrine-type alkaloidsCHEMONTID:0002723Lupin alkaloids with a structure based on the anagyrine skeleton. Anagyrine is a tetracyclic ketone containing a quinolizidine, and two pyridine rings fused together to form dipyrido[1,2-a:1',2'-e][1,5]diazocin-4-one.
BenzodifuransCHEMONTID:0002740Organic heterocyclic compounds containing a to furan rings fused to a central benzene ring. They can be grouped in angular and linear benzodifurans.
Clavines and derivativesCHEMONTID:0002747Hydroxy and dehydro derivatives of 6,8-dimethylergolenes and the corresponding ergolines.
ErythrinanesCHEMONTID:0002780Erythrina alkaloids possessing either a 6-5-6-6-membered indoloisoquinoline core or a derivative thereof.
Homoerythrinane alkaloidsCHEMONTID:0002781Erythrina alkaloids predominantly possessing a 6-5-7-6-membered indolobenzazepine skeleton or a derivative thereof.
1,3-oxazinanesCHEMONTID:0002790Compounds contain an oxazinane ring with the nitrogen atom and the oxygen atom at positions 1 and 3, respectively.
Organoboron compoundsCHEMONTID:0002795Organic compounds containing a carbon-boron bond.
1,2,3-triazinanesCHEMONTID:0002796Triazinanes having three nitrogen ring atoms at the 1-, 2-, and 3- positions.
1,2,4-triazinanesCHEMONTID:0002797Triazinanes having three nitrogen ring atoms at the 1-, 2-, and 4- positions.
1,3,5-triazinanesCHEMONTID:0002798Triazinanes having three nitrogen ring atoms at the 1-, 3-, and 5- positions.
1,4-benzodithiinsCHEMONTID:0002807Organic heterocyclic compounds containing a benzene ring fused to a 1,4-dithiin ring.
1,2-benzodithiinsCHEMONTID:0002805Organic heterocyclic compounds containing a benzene ring fused to a 1,2-dithiin ring.
1,3-benzodithiinsCHEMONTID:0002806Organic heterocyclic compounds containing a benzene ring fused to a 1,3-dithiin ring.
2,3-benzodithiinsCHEMONTID:0002808Organic heterocyclic compounds containing a benzene ring fused to a 2,3-dithiin ring.
Cinnamic acid amidesCHEMONTID:0002810Amides of cinnamic acids. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid.
PhenylpropanesCHEMONTID:0002811Organic compounds containing a phenylpropane moiety.
DibenzothiophenesCHEMONTID:0002818Organic heterocyclic compounds with a structure containing a dibenzothiophene moiety, made up of two benzene rings fused to a central thiophene ring.
Isoflav-3-enesCHEMONTID:0002819Flavonoids with a structure based on the 3-phenylchromene skeleton, with a double bond between the C3 and C4 carbon atoms of the chromene moiety.
Leontidine-type alkaloidsCHEMONTID:0002822Lupin alkaloids with a structure based on the leontidine skeleton, a tetracyclic compound containing fused piperidine, pyridine, and pyrrolidine rings.
Aloperine and related alkaloidsCHEMONTID:0002823Lupin Alkaloids with a structure based on the aloperine skeleton. Aloperine is a tetracyclic compound made up of a quinolizidine and a decahydroquinoline joined to form 3,15-diazatetracycloheptadecane.
OlefinsCHEMONTID:0002838Acyclic and cyclic hydrocarbons having one or more carbon-carbon double bonds, apart from the formal ones in aromatic compounds. The class of olefins subsumes alkenes and cycloalkenes and the corresponding polyenes.
AcetylenesCHEMONTID:0002843Acyclic (branched or unbranched) and cyclic (with or without side chain) hydrocarbons having one or more carbon to carbon triple bonds.
CytochalasinsCHEMONTID:0002852Cytochalasans in which the hydrogenated isoindolone bears a benzyl group.
AziridinonesCHEMONTID:0002853Compounds with a structure containing an aziridines ring bearing one carbonyl group. They are cyclic amides of acetic acid.
IsofamidesCHEMONTID:0002858Oxazaphospholanes containing the isofamide skeleton. Isofamide is a heterocyclic compound made up of a 1,3,2-oxazaphospholane, where the phosphorus atom is part of a phosphodiamide group, and the oxazaphospholane is substituted by two haloalkyl chains.
SulfonylaminesCHEMONTID:0002860Compounds having the general structure RN=S(=O)2.
Vinyl fluoridesCHEMONTID:0002861Vinyl halides in which a fluorine atom is bonded to an sp2-hybridised carbon atom.
Vinyl iodidesCHEMONTID:0002862Vinyl halides in which a iodine atom is bonded to an sp2-hybridised carbon atom.
Vinyl chloridesCHEMONTID:0002863Vinyl halides in which a chlorine atom is bonded to an sp2-hybridised carbon atom.
Vinyl bromidesCHEMONTID:0002864Vinyl halides in which a bromine atom is bonded to an sp2-hybridised carbon atom.
Actinide metavanadatesCHEMONTID:0002891Inorganic compounds in which the largest oxoanion is metavanadate, and in which the heaviest atom not in an oxoanion is an actinide.
QuinoniminesCHEMONTID:0002892Imines derived from quinones by replacement of one or both oxygens by =NR.
Isoflavonoid C-glycosidesCHEMONTID:0002896C-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.
Neoflavonoid 5-O-glycosidesCHEMONTID:00028975-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
MilbemycinsCHEMONTID:0002902A group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.g. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species.
HolostanesCHEMONTID:0002904Steroids with a structure characterized by a lanostane moiety possessing a 18,20-lactone ring.
1,2-dithiolesCHEMONTID:0003624Compounds containing a 5-membered unsaturated ring with three carbon atoms and two adjacent sulfur atoms.
BorinanesCHEMONTID:0002910Organic heterocyclic compounds containing a saturated aliphatic six-membered ring consisting of five carbon atoms and one boron atom.
HydroxyflavonoidsCHEMONTID:0002991Flavonoids in which one or more hydroxyl groups are attached to the flavonoid skeleton.
PhenyltropanesCHEMONTID:0002919Compounds containing a phenyl group linked to a tropane moiety. Tropane is an organonitrogenous [3.2.1] bicyclic organic compound.
1,2-diazepanesCHEMONTID:0002921Diazepanes having the two nitrogen atoms at position 1 and 2 of the diazepane ring.
1,3-diazepanesCHEMONTID:0002922Diazepanes having the two nitrogen atoms at position 1 and 3 of the diazepane ring.
1,4-diazepanesCHEMONTID:0002923Diazepanes having the two nitrogen atoms at position 1 and 4 of the diazepane ring.
Ortho estersCHEMONTID:0002926Compounds having the general structure RC(OR')3 ( R' not H), or the structure C(OR')4 ( R' not H).
Ortho amidesCHEMONTID:0002927Hypothetical Compounds having the general structure RC(NH2)3, and N-substituted derivatives thereof.
Ortho acidsCHEMONTID:0002928Ortho acid derivatives of carboxylic acids, with the general formula RC(OH)3.
1,3-isoquinolinedionesCHEMONTID:0002932Isoquinoline derivatives carrying one C=O group at positions 1, and 3 respectively.
1,4-isoquinolinedionesCHEMONTID:0002933Isoquinoline derivatives carrying a C=O group at positions 1 and 4, respectively.
Neoflavonoid 7-O-glycosidesCHEMONTID:00029357-O-glycosylated neoflavonoids. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
1,2-dioxepinesCHEMONTID:0002940Dioxepines with the two ring oxygen atoms at position 1 and 2, respectively.
1,3-dioxepinesCHEMONTID:0002941Dioxepines with the two ring oxygen atoms at position 1 and 3, respectively.
1,4-dioxepinesCHEMONTID:0002942Dioxepines with the two ring oxygen atoms at position 1 and 4, respectively.
1,2-dioxepanesCHEMONTID:0002944Dioxepanes with the two ring oxygen atoms at position 1 and 2, respectively.
1,3-dioxepanesCHEMONTID:0002945Dioxepanes with the two ring oxygen atoms at position 1 and 3, respectively.
1,4-dioxepanesCHEMONTID:0002946Dioxepanes with the two ring oxygen atoms at position 1 and 4, respectively.
PiperidinesulfonamidesCHEMONTID:0002953Organic compounds containing a sulfonamide group linked to a piperidine ring.
1-phenyltetrahydroisoquinolinesCHEMONTID:0002956Compounds containing a phenyl group attached to the C1-atom of a tetrahydroisoquinoline moiety.
4-phenyltetrahydroisoquinolinesCHEMONTID:0002957Compounds containing a phenyl group attached to the C4-atom of a tetrahydroisoquinoline moiety.
Tetracarboxylic acids and derivativesCHEMONTID:0002966Carboxylic acids containing exactly four carboxyl groups.
Hexacarboxylic acids and derivativesCHEMONTID:0002967Carboxylic acids containing exactly six carboxyl groups.
Delta-1-steroidsCHEMONTID:0002976Steroids containing a double bond between positions 1 and 2.
Delta-1,4-steroidsCHEMONTID:0002977Steroids containing a double bond between positions 1 and 2, as well as positions 4 and 5.
Delta-4-steroidsCHEMONTID:0002978Steroids containing a double bond between positions 4 and 5.
Delta-5-steroidsCHEMONTID:0002979Steroids containing a double bond between positions 5 and 6.
N-phenylthioureasCHEMONTID:0002980Compounds containing a N-phenylthiourea moiety, which is structurally characterized by a phenyl group linked to one nitrogen atom of a thiourea group.
Delta-7-steroidsCHEMONTID:0002984Steroids containing a double bond between positions 7 and 8.
Pentacarboxylic acids and derivativesCHEMONTID:0002995Carboxylic acids containing exactly five carboxyl groups.
Sulfated flavonoidsCHEMONTID:0003005Flavonoids that are sulfated at one or more positions.
PhenanthrolsCHEMONTID:0003007Compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached.
Phosphinic acid estersCHEMONTID:0003015Compounds containing a phosphinic acid ester group.
Hydroxy-7-aporphinesCHEMONTID:0003021Aporphines containing a hydroxyl group at the 7-position.
Methyl-7-aporphinesCHEMONTID:0003022Aporphines containing a methyl group at the 7-position.
N-acylpyrrolidinesCHEMONTID:0003023N-Acylated Pyrrolidine derivatives. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
Organic nitroso compoundsCHEMONTID:0004776Organic compounds having the nitroso group, -NO, attached to carbon, or to another element, most commonly nitrogen or oxygen.
C24-propyl sterols and derivativesCHEMONTID:0003061Sterols that carry a hydroxyl group at the 3-position, and a propyl group at the 24-position of the steroid backbone.
Indan-1-spirocyclohexanesCHEMONTID:0003065Organic aromatic compounds containing a cyclohexane moiety linked to the 1-position of an indane moiety in a spiro configuration.
Thioamide-S-oxidesCHEMONTID:0003076Organic compounds with the general formula RC(N)=[S+][O-] (R = organyl).
Thioamide-S,S-dioxidesCHEMONTID:0003077Organic compounds with the general formula RC(N)=[S+]([O-])(=O) (R = organyl).
N-sulfonyloxaziridinesCHEMONTID:0003093N-sulfonyl derivatives of oxaziridines, which are compounds containing a three-membered ring made up of an oxygen atom, a carbon atom, and a nitrogen atom.
FlavaglinesCHEMONTID:0003109Heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton.
Imidocarbonyl compoundsCHEMONTID:0003125Organic compounds with the general formula N=C(R)R' (R=organyl, R' = H or organyl).
Carboselenoic acidsCHEMONTID:0003126Organic compounds containing at least one carboselenoyl group, with the formula RC(=O)SeH.
CarboselenoamidesCHEMONTID:0003127Organic acid amide with the general formula RC(Se)NH2 (R=H, organic group).
CarbotelluroamidesCHEMONTID:0003129Organic acid amide with the general formula RC(Te)NH2 (R=H, organic group).
Hydrazinecarboxylic acids and derivativesCHEMONTID:0003132Organonitrogen compounds with the general formula RN(H)N(H)C(=O)OR' (R = organyl, R = any).
Aminosulfonyl compoundsCHEMONTID:0003137Organosulfur compounds with the general formula RS(=O)(=O)N(R')R'' (R = organyl, R'-R\" = any atom but N).
Hydrazinosulfonyl compoundsCHEMONTID:0003138Hydrazine derivatives with the general formula RS(=O)(=O)N(H)N (R = organyl).
Aminosulfinyl compoundsCHEMONTID:0003143Organic sulfinyl compounds with the general formula RS(=O)N(R')R\" (R=organyl; R'-R\" = any atom but N).
CarboximidamidesCHEMONTID:0003152Organonitrogen compounds with the general formula RN=CN(R')(R''), (R,R',R'' = H or organyl group).
CarboximidohydrazidesCHEMONTID:0003153Organonitrogen compounds with the general formula HN(H)N(H)C(H)=NR' (R' = H or organyl).
OS-thioperoxolsCHEMONTID:0003157Thioperoxols with the general formula R-OSH (R = organyl group).
SO-thioperoxolsCHEMONTID:0003158Thioperoxols with the general formula R-SOH (R = organyl group).
Coumarino-alpha-pyronesCHEMONTID:0003190Organic compounds with a structure characterized by the presence of a pyrano[3,2-c]chromene that carries two ketone groups at the 2- and 5-positions.
Coumarino-gamma-pyronesCHEMONTID:0003191Organic compounds with a structure characterized by the presence of a pyrano[3,2-c]chromene that carries two ketone groups at the 4- and 5-positions.
Nitrile ylidesCHEMONTID:00031931,3-Dipolar Compounds having the general structure RC#[N+][C-], R[C-]=[N+]=C, R[C+]=N[C-].
Sulfonyl azidesCHEMONTID:0003199Organosulfur compounds with the general formula RS(=O)(=O)N=[N+][N-] (R = organyl).
Carbo-azosulfonesCHEMONTID:0003209Organosulfur compounds with the general formula RS(R')(=N)=O (R,R' = alkyl groups).
Thiophene sulfoxidesCHEMONTID:0003215Organosulfur compounds containing a thiophene ring carrying a S=O bond (in some cases, a [S+][O-]).
3-aroylthiophenesCHEMONTID:0003216Thiophenes which are substituted by an aroyl group at the 3-position.
3-aroylfuransCHEMONTID:0003218Compounds containing a furan moiety which is acylated at the 3-position with an aromatic moiety.
Borinic acid estersCHEMONTID:0003220Compounds comprising the boronic acid ester functional group RB(R')OR'' (R,R',R''=organyl; X= any O,N,Hal residue).
Borinic acidsCHEMONTID:0003221Compounds comprising any derivative of the boronic acid functional group, with the general structure RB(R')OH (R,R'=organyl).
5,6-epoxysteroidsCHEMONTID:0003250Steroid derivatives sharing two carbon atoms at the 5- and 6- positions with an epoxide ring.
Sulfenyl halidesCHEMONTID:0003261Organosulfur compounds with the general formula RSX (R = organyl, X = halogen atom).
Sulfinyl halidesCHEMONTID:0003262Organosulfur compounds with the general formula RS(=O)X (R = organyl, X = halogen atom).
Glycerol vinyl ethersCHEMONTID:0003264Lipids containing a vinyl ether derivative of glycerol.
Isocyanide dichloridesCHEMONTID:0003272Organonitrogen compounds derived from isocyanide, with the general formula RN=C(Cl)Cl (R = organyl).
Idoso compoundsCHEMONTID:0003274Organoiodide compounds with the general formula RI=O (R = organyl group).
Idoxy compoundsCHEMONTID:0003275Organoiodide compounds with the general formula RI(OH)OH (R = organyl group).
YnolatesCHEMONTID:0003279Organooxygen compounds with the general formula R=C=O (R = organyl).
N-arylamidesCHEMONTID:0003282Organic compounds that contain a carboxamide group that is N-linked to a aryl group. They have the generic structure RC(=O)N(R')H, R = organyl group and R'= aryl group.
Alkali metal metavanadatesCHEMONTID:0003285Inorganic compounds in which the largest oxoanion is metavanadate, and in which the heaviest atom not in an oxoanion is an alkali metal.
Non-metal orthovanadatesCHEMONTID:0003290Inorganic non-metallic compounds containing a orthovanadate as its largest oxoanion.
Non-metal metavanadatesCHEMONTID:0003291Inorganic non-metallic compounds containing a metavanadate as its largest oxoanion.
Post-transition metal metavanadatesCHEMONTID:0003292Inorganic compounds in which the largest oxoanion is metavanadate, and in which the heaviest atom not in an oxoanion is a post-transition metal.
Transition metal metavanadatesCHEMONTID:0003293Inorganic compounds in which the largest oxoanion is metavanadate, and in which the heaviest atom not in an oxoanion is a transition metal.
Organic metavanadatesCHEMONTID:0003294Organic compounds containing the metavanadate oxoanion, with the formula [VO4]3-.
Polysaccharide sulfatesCHEMONTID:0003309Carbohydrates containing more than 10 sugar units, one of which bear one or more sulfate groups.
Naphthalene sulfonic acids and derivativesCHEMONTID:0003597Organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group (or a derivative thereof) at one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
PyridyltriazolesCHEMONTID:0003317Organic compounds containing a pyridine ring attached to a triazole ring.
Glycero-3-phosphosulfocholinesCHEMONTID:0003853Lipids containing a glycerol moiety carrying a phosphosulfocholine at the 3-position.
4,5-dioxoaporphinesCHEMONTID:0003326Alkaloids that contains the tetracyclic aporphine skeleton with two C=O groups at the 4- and 5-positions.
Thieno[3,4-c]pyridazinesCHEMONTID:0003353Organic heterocyclic compounds consisting of a thieno[3,4-c]pyridazine moiety. Thieno[3,4-c]pyridazine is a bicyclic compound made up of a thiophene ring fused to a pyridazine ring so that the sulfur atom and the two nitrogen atoms are at the 1-, 5-, and 6-position, respectively.
Thieno[3,4-d]pyridazinesCHEMONTID:0003354Organic heterocyclic compounds consisting of a thieno[3,4-d]pyridazine moiety. Thieno[3,4-d]pyridazine is a bicyclic compound made up of a thiophene ring fused to a pyridazine ring so that the sulfur atom and the two nitrogen atoms are at the 1-, 4-, and 5-position, respectively.
Pyrazinium compoundsCHEMONTID:0003361Organic aromatic compounds containing a pyriazinium ring.
Steroid acidsCHEMONTID:0003364Compounds containing a carboxyl group attached to a steroid backbone.
IsodiazenesCHEMONTID:0003371Organonitrogen compounds with the formula RN(R')N or R[N+](R')N-, where R and R' are organic groups.
1,2-dithiolanesCHEMONTID:0003372Organic compounds containing a 1,2-dithiolane ring. 1,2-dithiolane moiety is a 5-membered saturated aliphatic ring with three carbon atoms, and two sulfur atoms at the 1- and 2- ring positions.
1,3-dithiolanesCHEMONTID:0003373Organic compounds containing a 1,3-dithiolane ring. 1,3-dithiolane moiety is a 5-membered saturated aliphatic ring with three carbon atoms, and two sulfur atoms at the 1- and 3- ring positions.
Dithiolanecarboxylic acidsCHEMONTID:0003378Organic heterocyclic compounds containing a dithiolane ring that bears one or more carboxylic acids.
Dithiophosphate S-estersCHEMONTID:0003387S-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group).
PhosphonosphingolipidsCHEMONTID:0003391Sphingolipids with a structure based on a sphingoid base that is attached to a phosphonate head group. They differ from Phosphosphingolipids which have a phosphate head group.
(3'->5')-dinucleotidesCHEMONTID:0003394Dinucleotides where the two bases are connected via a (3'->5')-phosphodiester linkage.
5'-phospho-(2'->5')-dinucleotidesCHEMONTID:0003395(2'->5')-dinucleotides in which one of the based bears a phosphate group (or a phosphate chain) at the 5'-position.
PhosphatidylethanolsCHEMONTID:0003404Glycerophospholipids where the central glycerol is acylated at the 1- and 2-positions by two acyl chains, and is linked at the 3-position to a phosphoethanol. They are phospholipids formed only in the presence of ethanol via the action of phospholipase D.
3-arylcoumarin flavonoidsCHEMONTID:0003406Isoflavonoids that bear a ketone group at the C2-position.
Peltogynoid flavonoidsCHEMONTID:0003407Flavonoid compounds with a structure based on the isochromeno[4,3-b]-chromene skeleton. This skeleton results from the fusion of an isochromene to a chromene ring system.
2-benzopyransCHEMONTID:0003411Organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.
2-benzothiopyransCHEMONTID:0003414Organic aromatic compounds that 1-benzothiopyran, a bicyclic compound made up of a benzene ring fused to a thiopyran, so that the sulfur atom is at the 2-position.
9,9p-dihydroxyaryltetralin lignansCHEMONTID:0003426Lignans with a structure based on the 1-phenyltetralin skeleton carrying a hydroxyl group at the 9- and the 9'- position.
Tuberostemospironine-type alkaloidsCHEMONTID:0003916Alkaloids with a structure that is characterized by a 2H-spiro[furan-2,9A[9H]pyrrolo[1,2-a]azepin]-\n5-one nucleus which displays a spiro gamma-lactone at C-9 of the basic ring.
Stemoamide-type alkaloidsCHEMONTID:0003914Alkaloids which include a tricyclic 2H-furo[3,2-c]pyrrolo[1,2-a]azepine nucleus.
Dithiocarboxylic acids and derivativesCHEMONTID:0003436Organic compounds containing a dithiocarboxylic acid with the general formula RC(=S)SR' (R = organyl group, R' = H or organyl group).
S-alkyl thiosulfatesCHEMONTID:0003443Organosulfur compounds that contain a alkyl chain that is attached to the sulfur atom of thiosulfuric acid (or its conjugated base).
N-alkylpyrrolidinesCHEMONTID:0003449Compounds containing a pyrrolidine moiety that is substituted at the N1-position with an alkyl group. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
Alkyl sulfatesCHEMONTID:0003456Organic compounds containing a sulfate group that carries an alkyl group through an ether group.
Alkanesulfinic acids and derivativesCHEMONTID:0003461Organosulfur compounds containing an aliphatic group attached to a sulfinic acid group (or a derivative thereof), with the general formula RSO2R' (R= alkyl, R'=any atom).
Thiolane-2-thionesCHEMONTID:0003463Organic heterocyclic compounds containing a thiolane ring that carries a thione group at the 2-position. Thiolane is a five-membered saturated aliphatic ring made up of one sulfur atom and four carbon atoms.
Thiolane-3-thionesCHEMONTID:0003464Organic heterocyclic compounds containing a thiolane ring that carries a thione group at the 3-position. Thiolane is a five-membered saturated aliphatic ring made up of one sulfur atom and four carbon atoms.
p-Dioxolo[2,3-g]coumarinsCHEMONTID:0003465Organic aromatic compounds that contain a p-dioxole ring that is linearly fused to the benzene ring of a coumarin.
p-Dioxolo[2,3-h]coumarinsCHEMONTID:0003466Organic aromatic compounds that contain a p-dioxole ring that is angularly fused to the benzene ring of a coumarin. In p-dioxolo[2,3-h]coumarins, the coumarin ring system shares its C7-C8 bond with the p-dioxole ring.
CoumaronochromenesCHEMONTID:0003470Isoflavonoids with a structure characterized by the presence of a benzopyran and a benzofuran, with the particularity that the pyran and the furan ring are fused to each other.
AuronolsCHEMONTID:0003471Aurone flavonoids in which the pyran ring of the aurone skeleton carries a hydroxyl group at the 2-position.
Cinnamic acid estersCHEMONTID:0003480Compound containing an ester derivative of cinnamic acid.
2,5-disubstituted thiophenesCHEMONTID:0003481Organic compounds containing a thiophene that is disubstituted at the C-2, and C5-positions.
2,3,5-trisubstituted thiophenesCHEMONTID:0003482Organic compounds containing a thiophene that is trisubstituted at the C-2, C3- and C5-positions.
PyranocoumarinsCHEMONTID:0003484Organic compounds containing a pyran (or a hydrogenated derivative) fused to a coumarin moiety.
CinnamylphenolsCHEMONTID:0003496Organic compounds containing the 1,3-diphenylpropene moiety with one benzene ring bearing one or more hydroxyl groups.
4-prenylated 2-arybenzofuransCHEMONTID:00035112-arylbenzofuran flavonoids featuring a C5-isoprenoid unit at the 4-position.
7-prenylated 2-arybenzofuransCHEMONTID:00035152-arylbenzofuran flavonoids featuring a C5-isoprenoid unit at the 7-position.
4'-prenylated 2-arybenzofuransCHEMONTID:00035162-arylbenzofuran flavonoids featuring a C5-isoprenoid unit at the 4'-position.
PyranoflavonoidsCHEMONTID:0003520Compounds containing a pyran ring fused to a 2-phenyl-1,4-benzopyran skeleton.
PyranoisoflavonoidsCHEMONTID:0003530Isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.
DinaphthofuransCHEMONTID:0003536Organic aromatic compounds that contain two naphthalene moieties fused to each other through a furan ring. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.
Imidazo-[4,5-c]pyridinesCHEMONTID:0003590Organic heterocyclic compounds containing an imidazo-[4,5-c]pyridine ring system. Imidazo-[4,5-c]pyridine consists of an imidazole ring fused to a pyridine, so that the three ring nitrogen atoms are at the 1-, 2-, and 5-position, respectively.
Sulfinyl sulfonesCHEMONTID:0003591Organic compounds containing a sulfinyl sulfone group, with the general structure RS(=O)S(R')(=O)=O or RS(=O)(=O)S(R')=O (R=organyl group, R'=H or organyl group).
Phenanthro-perylenequinonesCHEMONTID:0003592Natural compounds or derivatives thereof that contain the phenanthroperylenequinone skeleton. Phenanthroperylenequinone is an octacyclic compound consisting of 2 1-hydroxy-9,10-dihydroanthracen-9-one ring system joined to each other with a naphthalene.
Pyridoazepine alkaloidsCHEMONTID:0003594Alkaloids are characterized by a pyrido[1,2- a]azepine nucleus usually linked with two carbon chains mostly forming terminal lactone rings. These compounds are believed to be derived from a protostemonine-type precursor have been discovered.
1,2-diacyl-sn-glycerol-3(2'-aminopropyl)phosphonatesCHEMONTID:0003615Lipids that contain an aminopropylphosphonate group attached at a C3 carbon of a 1,2-diacylglycerol backbone.
GlycerophosphonocholinesCHEMONTID:0003620Lipids that contain a phosphonocholine group linked to a terminal carbon of a glycerol moiety.
GlycerophosphonoethanolaminesCHEMONTID:0003621Lipids that contain a phosphonoethanolamine group linked to a terminal carbon of a glycerol moiety.
1,3-dithiolesCHEMONTID:0003625Compounds containing a 5-membered unsaturated ring with three carbon atoms, and two sulfur atoms at the 1- and 3-positions, respectively.
Acyl carbenesCHEMONTID:0003634Any compound with the general structure acyl-C:-R. In organic chemistry, an unspecified acyl carbene is commonly a carboxylic acyl carbene RC(=O)-C:-R.
Imidoyl carbenesCHEMONTID:0003635Carbenes having the structure RC(=NR)C:-R.
Vinyl carbenesCHEMONTID:0003636Carbenes having a vinylic group on a carbenic carbon atom R2C=CRC:R <-> R2C+-CR=C-R.
Flav-3-enesCHEMONTID:0003637Flavonoids with a structure based on the 2-phenylchromene skeleton, with a double bond between the C3 and C4 carbon atoms of the chromene moiety.
5-prenylated 2-arybenzofuransCHEMONTID:00036492-arylbenzofuran flavonoids featuring a C5-isoprenoid unit at the 5-position.
Prenylated neoflavonoidsCHEMONTID:0003650Neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
PyranoneoflavonoidsCHEMONTID:0003652Compounds containing a pyran ring fused to either ring A, B, or C of the neoflavonoid skeleton. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.
1,1'-azonaphthalenesCHEMONTID:0003653Organonitrogen aromatic compounds that contain a central azo group, where each nitrogen atom is conjugated to the 1-position of a naphthalene ring system. Naphthalene is a compound made up of two fused benzene rings.
Allyl-type 1,3-dipolar inorganic compoundsCHEMONTID:0003668Inorganic 1,3-dipolar compounds with the general structure X=Y+-Z- <-> X--Y+=Z<-> X+-Y-Z-<-> X-=Y-Z+ (X, Z = N, or O; Y = N or O).
Propargyl-type 1,3-dipolar inorganic compoundsCHEMONTID:00036691,3-dipolar compounds with the general structure X#N+-Z- <-> X-=N+=Z <-> X-=N-Z+ <-> X-N=Z (X =O, Z =N, or O).
Enol ester epoxidesCHEMONTID:0003676Epoxide containing derivatives of enol esters. They have an acyloxy substituent on either carbon atom of the epoxide ring and their general structure is CC1OC1OC(R)=O, R = H or organyl chain.
ThioflavansCHEMONTID:0003683Compounds containing a thiochromane skeleton substituted at the 2-position with a phenyl group.
Nitrile oxidesCHEMONTID:0003687Ylides having the structure RC#[N+][O-] or R[C-]=[N+]=O.
Diazo compoundsCHEMONTID:0003688Organic compounds having the divalent diazo group, =N+=N-, attached to a carbon atom.
Nitrile sulfidesCHEMONTID:0003689Sulfur analogues of nitrile oxides with the general structure RC#[N+][S-] or R[C-]=[N+]=S.
1,2-diseleninsCHEMONTID:0003692Organic heterocyclic compounds containing a 1,2-diselenin ring. Diselenin is a six-membered heterocyclic with for carbon atoms, and two selenium atoms at the 1- and 2-position.
1,3-diseleninsCHEMONTID:0003693Organic heterocyclic compounds containing a 1,3-diselenin ring. Diselenin is a six-membered heterocyclic with for carbon atoms, and two selenium atoms at the 1- and 3-position.
1,4-diseleninsCHEMONTID:0003694Organic heterocyclic compounds containing a 1,4-diselenin ring. Diselenin is a six-membered heterocyclic with for carbon atoms, and two selenium atoms at the 1- and 4-position.
Nitrile selenidesCHEMONTID:0003695Organonitrogen compounds containing a nitrogen-selenium bond. They have the general structure R-C#NSe, where R = any atom.
Organic thionylimidesCHEMONTID:0003699Organic compounds that contain the thionylimide group (N=S=O).
2-pyranosylbenzoxazolesCHEMONTID:0003703Nucleoside and nucleotide analogs with a structure that consists of a benzoxazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
2-pyranosylbenzothiazolesCHEMONTID:0003704Nucleoside and nucleotide analogs with a structure that consists of a benzothiazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
2-ribofuranosylbenzimidazolesCHEMONTID:0003705Nucleoside and nucleotide analogs with a structure that consists of a benzimidazole ring system which is N-substituted at the 2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
2-pyranosylbenzimidazolesCHEMONTID:0003706Nucleoside and nucleotide analogs with a structure that consists of a benzimidazole which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
1-pyranosylbenzimidazolesCHEMONTID:0003708Nucleoside and nucleotide analogs with a structure that consists of a Benzimidazole which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
2-ribofuranosylbenzotriazolesCHEMONTID:0003709Nucleoside and nucleotide analogs with a structure that consists of a benzotriazole ring system which is N-substituted at the 2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
1-pyranosylbenzotriazolesCHEMONTID:0003710Nucleoside and nucleotide analogs with a structure that consists of a Benzotriazole which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
2-pyranosylbenzotriazolesCHEMONTID:0003711Nucleoside and nucleotide analogs with a structure that consists of a benzotriazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
2-ribofuranosylindazolesCHEMONTID:0003712Nucleoside and nucleotide analogs with a structure that consists of an indazole ring system which is N-substituted at the 2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
1-pyranosylindazolesCHEMONTID:0003713Nucleoside and nucleotide analogs with a structure that consists of an indazole which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
2-pyranosylindazolesCHEMONTID:0003714Nucleoside and nucleotide analogs with a structure that consists of an indazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
1-pyranosylindolesCHEMONTID:0003715Nucleoside and nucleotide analogs with a structure that consists of an indole base which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
3-ribofuranosylpyrazolesCHEMONTID:0003716Nucleoside and nucleotide analogs with a structure that consists of a pyrazole ring system which is N-substituted at the 3-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
Cyclopropyl nucleosidesCHEMONTID:0003741Nucleoside analogues with a structure that consists of a cyclopropane that is substituted a the 1-position with a hydroxyl group and at the 2- position with either a purine or pyrimidine base.
Cyclobutyl nucleosidesCHEMONTID:0003723Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3- position with either a purine or pyrimidine base.
Phosphonated cyclopentyl nucleosidesCHEMONTID:0003724Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 2- or the 3- position with either a purine or pyrimidine base.
Acyclic 2,4-diaminopyrimidine nucleoside phosphonatesCHEMONTID:0003725Pyrimidine nucleoside analogues with a structure that is characterized by a phosphonylmethoxyethoxyl group that is linked to the N1 atom of a 2,4-diaminopyrimidine.
Acyclic purine nucleoside phosphonatesCHEMONTID:0003726Purine nucleoside analogues with a structure that is characterized by a phosphonylmethoxyethoxyl group that is linked to the N1 atom of a purine.
Phosphonated cyclopropyl nucleosidesCHEMONTID:0003744Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group and at the 2-position with either a purine or pyrimidine base.
Phosphonated 2'-oxa,3'-aza purine nucleosidesCHEMONTID:0003733Nucleoside and nucleotide analogues with a structure that consists of a purine base, which N-substituted at the 1-position with a 3'-aza derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides. Moreover, a phosphonate group s attached to the C4-atom of the resulting 1.3-oxazolidine.
Phosphonated 2'-oxa,3'-aza pyrimidine nucleosidesCHEMONTID:0003734Nucleoside and nucleotide analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-aza derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides. Moreover, a phosphonate group s attached to the C4-atom of the resulting 1.3-oxazolidine.
C2-linked imidazole ribonucleosides and ribonucleotidesCHEMONTID:0003735Nucleoside and nucleotide analogues with a structure that consists of an imidazole ring system which is substituted at the C2-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
C4-linked imidazole ribonucleosides and ribonucleotidesCHEMONTID:0003736Nucleoside and nucleotide analogues with a structure that consists of an imidazole ring system which is substituted at the C4-position with a ribose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the furanose.
Cyclopentyl nucleosidesCHEMONTID:0003738Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 2- or the 3- position with either a purine or pyrimidine base.
3'-thia pyrimidine nucleosidesCHEMONTID:0003746Nucleoside analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-thia derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides.
PyrichalasinsCHEMONTID:0003766Cytochalasans with a structure in which the hydrogenated isoindole bears p-methoxybenzyl group.
ChaetoglobosinsCHEMONTID:0003767Cytochalasans with a structure in which the hydrogenated isoindole bears an (indol-3-yl)methyl group.
AspochalasinsCHEMONTID:0003768Cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group.
AlachalasinsCHEMONTID:0003769Cytochalasans with a structure in which the hydrogenated isoindole bears a methyl group.
Imidazo[5,1-d]-1,2,3,5-tetrazinesCHEMONTID:0003771Organic aromatic compounds consisting of an imidazole fused to a 1,2,3,5-tetrazine. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. 1,2,3,5-tetrazine is a six-membered aromatic heterocycle made up of four nitrogen atoms at the 1-, 2-, 3-,and 5-positions, as well as and a two carbon atoms.
4,6-disubstituted quinolizidinesCHEMONTID:0003785Compounds containing a quinolizine ring system that is substituted only at the 4- and 6-positions. Some alkaloids possessing a quinolizidine disubstituted at the 4- and 6-positions with alkyl groups have been isolated.
1,4-disubstituted quinolizidinesCHEMONTID:0003786Compounds containing a quinolizine ring system that is substituted only at the 1- and 4-positions. Some alkaloids possessing a quinolizidine disubstituted at the 1- and 4-positions with alkyl groups have been isolated.
(3'->5')-cyclic dinucleotides and analoguesCHEMONTID:0003792Cyclic compounds consisting of two ribose moieties connected by two 5',3'-phosphodiester bonds to form a cycle. Each ribose unit is N-linked to a nucleic base or an analogue thereof. Some natural (3'->5')-cyclic dinucleotides include c-di-AMP. Synthetic derivatives are generally more elaborated molecules in which one or the two nucleobase moieties, and/or sugar residues, and/or phosphodiester linkers have been modified.
(3'->5')-dinucleotide phosphorothioatesCHEMONTID:0003797Compounds consisting of two ribose moieties connected one 5',3'-phosphomonothioic acid O,O'-diester bond. Each ribose unit is N-linked to a nucleic base or an analogue thereof.
(3'->5')-dinucleotide phosphorodithioatesCHEMONTID:0003798Compounds consisting of two ribose moieties connected by one 5',3'-phosphodithioate bond. Each ribose unit is N-linked to a nucleic base or an analogue thereof.
Phosphorothioate oligonucleotidesCHEMONTID:0003800Oligonucleotides in which one of the non-bridging oxygens in each phosphodiester linkage has been replaced by sulfur.
Purine nucleoside phosphorothioatesCHEMONTID:0003801Analogues of purine nucleoside monophosphates where the ribose unit is linked to a phosphorothioate group at the 5'-position, instead of a phosphate group.
Pyrimidine nucleoside phosphorothioatesCHEMONTID:0003802Analogues of pyrimidine nucleoside monophosphates where the ribose unit is linked to a phosphorothioate group at the 5'-position, instead of a phosphate group.
2',3'-cyclic purine nucleoside phosphorothioatesCHEMONTID:00038032',3'-cyclic purine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 2',3'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 2'- and 3'-positions of the ribose are part of the phosphorothioate group.
2',3'-cyclic pyrimidine nucleoside phosphorothioatesCHEMONTID:00038042',3'-cyclic pyrimidine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 2',3'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 2'- and 3'-positions of the ribose are part of the phosphorothioate group.
AlkyldiazohydroxidesCHEMONTID:0003835Organonitrogen compounds with the general formula RN=NOH, where R = organyl.
DialkylthioethersCHEMONTID:0003862Organosulfur compounds containing a thioether group that is substituted by two alkyl groups.
Aryl thioethersCHEMONTID:0004631Organosulfur compounds containing a thioether group that is substituted by an aryl group.
Imidothioic acidsCHEMONTID:0003883Sulfur derivatives of imidic acid containing the functional group -RC(=N)S, obtained by replacing the oxygen atom by a sulfur atom.
ImidothiolactonesCHEMONTID:0003885Analogs of imidolactones where the oxygen atom is replaced by a sulfur atom. They have the general structure RC(=N)SR' where the central carbon atom is part of a ring. R,R' = organyl group.
Cyclic imidoyl halidesCHEMONTID:0003887Imidoyl halides with the general formula R(X)C=NR' (R, R'=H, alkyl, aryl), where the central carbon atom is part of a ring.
Vinylogous halidesCHEMONTID:0003888Organic compounds containing a halogen atom, which is indirectly attached to a carbonyl via an intervening vinyl (>C=C<) moiety.
Organic phosphonic acid diamidesCHEMONTID:0003892Organophosphorus compounds containing a diamide derivative of phosphonic acid, with the general structure R1P(=O)(N(R2)R3)N(R4)R5, where R = organyl and R2-R5 = H or organyl group.
Phosphonic acid diestersCHEMONTID:0003893Organophosphorus compounds containing a diester derivative of phosphonic acid, with the general structure ROP(=O)OR' (R,R' = organyl group).
Phosphonic amide estersCHEMONTID:0003894Organophosphorus compounds containing a diester derivative of phosphonic acid amide, with the general structure ROP(=O)N(R')R\" (R = organyl group, R'-R\" = H or organyl group).
BromoalkenesCHEMONTID:0003904Compounds derived from an alkene by replacing a hydrogen atom with a bromine atom.
ChloroalkenesCHEMONTID:0003905Compounds derived from an alkene by replacing a hydrogen atom with a chlorine atom.
FluoroalkenesCHEMONTID:0003906Compounds derived from an alkene by replacing a hydrogen atom with a fluorine atom.
IodoalkenesCHEMONTID:0003907Compounds derived from an alkene by replacing a hydrogen atom with an iodine atom.
2-aroylquinolinesCHEMONTID:0003910Compounds containing a quinoline which carries an aroyl group at the 2-position. An aroyl group is a univalent radical R-CO- derived from an aromatic carboxylic acid.
4-aroylquinolinesCHEMONTID:0003912Compounds containing a quinoline which carries an aroyl group at the 4-position. An aroyl group is a univalent radical R-CO- derived from an aromatic carboxylic acid.
Stenine-type alkaloidsCHEMONTID:0003913Alkaloids which can be structurally represented by the tetracyclic\nfuro[2,3-h]pyrrolo[3,2,1-jk][1]benzazepin-10(2H)-one nucleus.
Stemonamine-type alkaloidsCHEMONTID:0003915Alkaloids with a structure characterized by the tetracyclic 2AH,11H-spiro[1H-cyclopenta-[b]pyrrolo[1,2-a]azepine-11,2A-furan]-5A,10-dione nucleus with a spirolactone ring at C-12.
Parvistemoline-type alkaloidsCHEMONTID:0003917Alkaloids that feature a conserved pyrrolo[1,2-a]azepine nucleus. They are characterized by a hexahydro-2,6-dimethyl-5-oxofuro[3,2-b]furan-3-yl moiety attached to C-9 in the pyrrolo[1,2-a]azepine nucleus.
Organic alkali metal saltsCHEMONTID:0004099Organic salts of an alkali metal. The alkali metal atom is usually in its ionic form.
Dithiocarbamic acidsCHEMONTID:0003935Organosulfur compounds with the general formula HSC(=S)N(R1)R2; R1-R2 = H or organyl group.
Dithiocarbamic acid estersCHEMONTID:0003936Organosulfur compounds with the general formula R3SC(=S)N(R1)R2; R1-R2 = H or organyl group, R3 = organyl.
Cyclic dithiocarbamatesCHEMONTID:0003937Organic compounds containing the dithiocarbamic acid group as part of a cycle.
Phosphine sulfidesCHEMONTID:0003938Compounds having the general formula R3P=S <=> R3P+S-.
Inorganic arsenidesCHEMONTID:0003941Inorganic compounds containing arsenic with one or more less electronegative elements.
8-hydroxyquinolinesCHEMONTID:0003953Compounds containing a quinoline moiety, which carries a hydroxy group at the 8-position. Quinoline consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.
HalopyridinesCHEMONTID:0003970Organic compounds containing a pyridine ring substituted at one or more positions by a halogen atom.
3-pyridinecarbonitrilesCHEMONTID:0003972Organic compounds containing a pyridine ring substituted at the 3-position by a carbonitrile group.
Organic nitrenesCHEMONTID:0003973Compounds containing a bond between a carbon and a nitrogen atom with only 2 pairs of unshared electrons.
Alkyldimethylbenzylammonium halidesCHEMONTID:0003976Organic compounds consisting of a quaternary ammonium group substituted with a benzyl group, two methyl groups as well as an alkyl chain. These compounds also contain a halogen ion and have the general structure R1[N+](CH3)(CH3)R2.[X-], where R1 = benzyl group, R2 = alkyl chain, and X = halogen atom.
Benzyl halidesCHEMONTID:0003981Organic compounds containing a benzene skeleton substituted with a halomethyl group.
Organic triazanesCHEMONTID:0003992Organic compounds containing the triazane group (NH2NHNH2) or a hydrocarbyl derivative thereof.
AminoxidesCHEMONTID:0003993Hydrocarbyl derivatives of the aminoxide anion, with the general formula R3N+[O-] or R3N=O.
Phosphonic dihydrazidesCHEMONTID:0003994Organic derivatives of phosphonic acid having the general formula RP(=O)(NHNH2)2, where the R is an organyl group and the hydrogen atoms can be replaced by an organyl group.
Organic transition metal saltsCHEMONTID:0003997Organic salt compounds containing a transition metal atom in its ionic form.
Organic metalloid saltsCHEMONTID:0003998Organic salt compounds containing a metalloid atom in its ionic form.
BenzazocinesCHEMONTID:0004007Organic compounds containing the benzazocine ring system, which consists of a benzene ring bound to an azocine ring.
HaloquinolinesCHEMONTID:0004403Compounds containing a quinoline moiety, which is substituted at one or more ring positions by n halogen atom.
Organocopper compoundsCHEMONTID:0004017Compounds containing a bond between a carbon atom and a copper atom.
Organolead compoundsCHEMONTID:0004024Compounds containing bond between a carbon atom and a lead atom.
Organosilver compoundsCHEMONTID:0004025Organic compounds containing a bond between a carbon atom and a silver atom.
Organic metal bromide saltsCHEMONTID:0004037Organic metal salts containing a bromine atom in its ionic form.
Organic post-transition metal saltsCHEMONTID:0004040Organic salt compounds containing a post-transition metal atom in its ionic form.
Trivalent inorganic arsenic compoundsCHEMONTID:0004053Inorganic compounds containing a trivalent arsenic atom.
Pentavalent inorganic arsenic compoundsCHEMONTID:0004054Inorganic compounds containing a pentavalent arsenic atom.
Organochromium compoundsCHEMONTID:0004073Compounds containing a bond between a carbon atom and a chromium atom.
VinylaziridinesCHEMONTID:0004079Compounds containing an aziridine ring substituted by one or more vinyl groups.
1-benzylquinolinesCHEMONTID:0004083Organic aromatic compounds containing a quinoline that is substituted at the 1-position by a benzyl group.
DialkyldisulfidesCHEMONTID:0004089Organic compounds containing a disulfide group R-SS-R' where R and R' are both alkyl groups.
1-phenethylisoquinolinesCHEMONTID:0004095Organic aromatic compounds containing a quinoline ring system substituted at the 1-position by a phenethyl group.
1,4-benzodiazepinesCHEMONTID:0004097Organic compounds containing a benzene ring fused to a 1,4-azepine.
1,3,5-triazinesCHEMONTID:0004105Compounds containing a triazine ring, which is a heterocyclic ring, similar to the six-member benzene ring but with three carbons replaced by nitrogen atoms, at ring positions 1, 3, and 5.
1,2,3-triazinesCHEMONTID:0004106Compounds containing a triazine ring, which is a heterocyclic ring, similar to the six-member benzene ring but with three carbons replaced by nitrogen atoms, at ring positions 1, 2, and 3.
1,2,4-triazinesCHEMONTID:0004107Compounds containing a triazine ring, which is a heterocyclic ring, similar to the six-member benzene ring but with three carbons replaced by nitrogen atoms, at ring positions 1, 2, and 4.
MethoxybenzenesCHEMONTID:0004113Organic aromatic compounds containing a monocyclic benzene moiety carrying exactly or one more methoxy groups.
Benzoyl peroxidesCHEMONTID:0004112Organic compounds containing two benzoyl groups O-linked to each other via a peroxide group. Their skeleton has the general formula [C6H5C(O)]2O2.
Alpha-imino acid and derivativesCHEMONTID:0004132Organic acids containing an imino group attached to a carbon, which in turn is immediately linked to a carboxyl group (or a derivative thereof).
N,S-acetalsCHEMONTID:0004116Organosulfur compounds with the generic structure RC(SR')N([H])C=O, where R,R'= H or organyl group.
OxoisoaporphinesCHEMONTID:0004118Alkaloids with a structure that contains the isoaporphine skeleton with an oxo group at the 7-position.
Lycorine-type amaryllidaceae alkaloidsCHEMONTID:0004120Amaryllidaceae alkaloids compounds containing the lycorine skeleton, made up of a pyrrolo[d,e]phenanthridine ring system.
Norbelladine-type amaryllidaceae alkaloidsCHEMONTID:0004121Amaryllidaceae alkaloids compounds containing the norbelladine skeleton. They are derived initially from the condensation of tyramine and protocatechuic aldehyde or its derivatives in plants.
Homolycorine-type amaryllidaceae alkaloidsCHEMONTID:0004122Amaryllidaceae alkaloids compounds containing the homolycorine skeleton, made up of a [3,4-g]benzopyranone ring due to the oxidation of the hydroxyl group at the C6. They are biogenetically formed through a restructuring of lycorine-type alkaloids.
Crinine- and Haemanthamine-type amaryllidaceae alkaloidsCHEMONTID:0004123Amaryllidaceae alkaloids compounds with a structure based on the crinine or haemanthamine backbone. Both backbones have a common 5,10b-ethano bridge moiety in their frameworks, which is a very significant taxonomic feature, and the configurations of the 5,10b-ethano bridge are opposite to each other.
Tazettine-type amaryllidaceae alkaloidsCHEMONTID:0004124Amaryllidaceae alkaloids derived from the haemanthamine-type alkaloids, which are characterized as a linkage between C6 and C11 by an oxygen atom to form a [3,4-g]benzopyran framework.
Montanine-type amaryllidaceae alkaloidsCHEMONTID:0004125Amaryllidaceae alkaloids based on the montanine skeleton, which is made up of a characteristic 5,11-methanomorphanthridine framework.
Plicamine-type amaryllidaceae alkaloidsCHEMONTID:0004126Dinitrogenous Amaryllidaceae alkaloids derived from tazettine-type alkaloids, by replacement of the oxygen atom at the C6 by a nitrogen atom, which is in turn substituted with a 4-hydroxyphenethyl unit. In addition, all alkaloids of this minor subgroup have an amide group on the C12.
Galanthindole-type amaryllidaceae alkaloidsCHEMONTID:0004127Amaryllidaceae alkaloids based on a 7-arylindole or 7-aryl-2,3-dihydroindole skeleton.
Galanthamine-type amaryllidaceae alkaloidsCHEMONTID:0004128Amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A.
Phenanthridine- and phenanthridone-type amaryllidaceae alkaloidsCHEMONTID:0004129Amaryllidaceae alkaloids compounds based on the phenanthridine or the phenanthridone skeleton. Phenanthridone-type alkaloids have the highest oxygenated C ring in all Amaryllidaceae alkaloids, and they always show an amide group in ring B. On the contrary, alkaloids of the phenanthridine type often show completely aromatic ring system, occasionally with a methylation quaternary nitrogen atom.
Gracilline-type amaryllidaceae alkaloidsCHEMONTID:0004130Amaryllidaceae alkaloids compounds containing a 10b,4a-ethanoiminodibenzo[b,d]pyrane skeleton.
EpithionitrilesCHEMONTID:0004134Organoheterocyclic compounds made up of a carbon atom linked to a thiirane ring and a carbonitrile group.
Thiohydroximic acidsCHEMONTID:0004137Organosulfur compounds with the general structure RC(S)=NOH, where R = H or organyl group.
HydroxypyridinesCHEMONTID:0004151Organic compounds containing a pyridine ring substituted at one or more positions by a hydroxyl group.
MethylpyridinesCHEMONTID:0004152Organic compounds containing a pyridine ring substituted at one or more positions by a methyl group.
HydroxyisoflavonoidsCHEMONTID:0004154Organic compounds containing an isoflavonoid skeleton carrying one or more hydroxyl groups.
HalomethanesCHEMONTID:0004157Organic compounds in which at least one of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
HydroxyindolesCHEMONTID:0004162Organic compounds containing an indole moiety that carries a hydroxyl group.
Dithiophosphate O-estersCHEMONTID:0004164O-ester derivatives of dithiophosphates, with the general structure RSP(O)(O)=S (R = organyl group).
QuindolinesCHEMONTID:0004168Organic compounds containing an indole and a quinoline, where the pyrrole moiety of the indole is fused to the pyridine moiety of the quinoline.
Flavonoid 3-phosphatesCHEMONTID:0004182Flavonoids that carry a phosphate group at the3-ring position of the flavonoid skeleton.
PhorbinesCHEMONTID:0004187Cyclic tetrapyrrole that consists of porphyrin that has a cyclopentane ring fused to one of the pyrrole rings and the adjacent methine group.
PhthalocyaninesCHEMONTID:0004188Cyclic tetrapyrroles that contain a phthalocyanine skeleton, which consists of four isoindole-type units, with the connecting carbon atoms in the macrocycle replaced by nitrogen.
1-phenylcoumaransCHEMONTID:0004190Compounds containing a coumaran ring system substituted at the 1-position with phenyl group.
14-alpha-methylsteroidsCHEMONTID:0004192Steroids substituted at the 14-position with a methyl group in the alpha-configuration.
Pyrrolo[1,2-a]benzimidazolesCHEMONTID:0004194Compounds containing a pyrrole or a dehydrogenated derivative fused to the imidazole moiety of a benzimidazole.
N-alkylindolesCHEMONTID:0004197Compounds containing an indole moiety that carries an alkyl chain at the 1-position.
DithiazinanesCHEMONTID:0004198Cyclic compounds that contain a dithiazinane ring, which is a saturated heterocycle that consisting of one nitrogen atom, two sulfur atoms, and 2 carbon atoms.
TriazolobenzothiazolesCHEMONTID:0004201Compound containing a triazole ring fused to the benzene or the thiazole moiety of the benzothiazole ring system.
Phenyl-beta-methoxyacrylatesCHEMONTID:0004203Aromatic compounds containing a methyl-3-methoxyacrylate moiety that carries a benzyl group at the C-alpha carbon.
XylenesCHEMONTID:0004208Aromatic compounds that contain a xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups.
1,4-oxathiin carboxamidesCHEMONTID:0004217Heterocyclic compounds containing a 1,4-oxathiin ring that carries a carboxamide group. 1,4-oxathiin is an unsaturated heterocycle where the carbon atoms at the 1-, and 4-positions are replaced by containing a sulfur atom and an oxygen atom, respectively.
Pyrrolo[1,2-c][1,3]benzodiazepinesCHEMONTID:0004229Heterocyclic aromatic compounds containing a 1,3-benzodiazepine ring system that is fused to, and shared a nitrogen atom with a pyrrole ring.
Benzenesulfonyl compoundsCHEMONTID:0004233Aromatic compounds containing a benzenesulfonyl group, which consists of a monocyclic benzene moiety that carries a sulfonyl group.
6,7-dihydropteridinesCHEMONTID:0004269Aromatic heterocyclic compounds containing 6,7-dihydropteridine, a bicyclic compound that results from the dehydrogenation of pteridine at the 6-, and 7-positions.
5,6,7,8-tetrahydropteridinesCHEMONTID:0004270Aromatic heterocyclic compounds containing 5,6,7,8-tetrahydropteridine, a bicyclic compound that results from the dehydrogenation of pteridine at the 5-, 6-, 7-and 8-positions.
1-benzothiophenesCHEMONTID:0004293Aromatic heterocyclic compound containing the Benzo[b]thiophene ring system.
2-benzothiophenesCHEMONTID:0004294Aromatic heterocyclic compound containing the 2-benzothiophene ring system, in which the benzene ring is fused to the thiophene ring across positions 3 and 4.
MetallobisdithiocarbamatesCHEMONTID:0004306Organosulfur compounds containing a metal atom (usually in ionic form), which is linked to two dithiocarbamate.
ImidazoquinolinesCHEMONTID:0004331Aromatic heterocyclic compounds containing an imidazole ring fused to a quinoline ring system. In some configurations, the imidazole ring shares a nitrogen atom with the quinoline moiety.
Imidazo[2,1-b]benzothiazolesCHEMONTID:0004332Aromatic heterocyclic compounds containing an imidazole ring fused to and sharing a nitrogen atom with a benzo-1,3-thiazole ring system.
NitrothiophenesCHEMONTID:0004336Aromatic heterocyclic compound containing a nitro group attached to a thiophene ring.
Dipyrido[1,4]diazepinesCHEMONTID:0004346Aromatic heteropolycyclic compounds containing two pyridines rings bound to a 1,4-diazepine ring.
Acyclic pyrimidine nucleoside phosphonatesCHEMONTID:0004349Purine nucleoside analogues with a structure that is characterized by a phosphonylmethoxyethoxyl group that is linked to the N1 atom of a purine.
OligonucleotidesCHEMONTID:0004351Organic polymers made up of a sequence of 3 to 12 purine or pyrimidine nucleotide residues linked to one another from the 5' -end to the 3'-end through a phosphate group.
Sulfono(thioperoxoic) SO-acidsCHEMONTID:0004356Organosulfur compounds with the general formula RSO2-SOH, where R is an organic substituent.
Sulfonothioic S-acidsCHEMONTID:0004358Organosulfur compounds with the general formula RS(O)(O)-SH, where R is an organic substituent.
Sulfonoperoxoic acidsCHEMONTID:0004359Organosulfur compounds with the general formula RSO2-OOH, where R is an organic substituent.
Sulfonoselenoic Se-acidsCHEMONTID:0004360Organosulfur compounds containing a selenium atom, and with the general formula RSI2-SeH, where R is an organic substituent.
Purine ribonucleoside phosphonatesCHEMONTID:0004362N-glycosyl compound that possess both a purine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.
Pyrimidine ribonucleoside phosphonatesCHEMONTID:0004363N-glycosyl compound that possess both a pyrimidine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.
Ribonucleoside phosphoramiditesCHEMONTID:0004364Ribonucleoside analogues that consist of a nucleobase (usually purine or pyrimidine), linked to a ribose or deoxyribose, which is protected at the 2',3', or 5'-position by a phosphoramidite group.
2-AnilinoquinolinesCHEMONTID:0004366Aromatic heteropolycyclic compounds containing a quinoline ring that is N-linked at the 2-position to an aniline.
3-AnilinoquinolinesCHEMONTID:0004367Compounds containing a quinoline ring system that is N-linked to an aniline group at the 3-position.
4-AnilinoquinolinesCHEMONTID:0004368Compounds containing a quinoline ring system that is N-linked to an aniline group at the 4-position.
Pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-4-onesCHEMONTID:0004383Aromatic heterocyclic compounds containing a pyrimidine fused to both a pyrazole and a pyridazine rings. The resulting ring system carries an oxo group at the 4-position. Here, the pyrimidine ring shares one atom with the pyrazole ring, and no nitrogen atom with the pyrazole ring.
2,4-Diaminothieno[2,3-d]pyrimidinesCHEMONTID:0004385Aromatic heterocyclic compounds containing a thieno[2,3-d]pyrimidine ring system substituted at the 2- and 4-positions with an amine group.
Pyrazolo[3,4-d]pyrimidinesCHEMONTID:0004387Aromatic heterocyclic compounds containing a pyrazolo[3,4-d]pyrimidine ring system, which consists of a pyrazole ring fused to but and not sharing a nitrogen atom with a pyrimidine ring.
Pyrazolo[1,5-a]pyrimidinesCHEMONTID:0004390Aromatic heterocyclic compounds containing a pyrazolo[3,4-d]pyrimidine ring system, which consists of a pyrazole ring fused to and sharing exactly one nitrogen atom with a pyrimidine ring.
7-oxo-1,3-thiazolo[5,4-d]pyrimidinesCHEMONTID:0004402Aromatic heteropolycyclic compounds containing a 1,3-thiazolo[5,4-d]pyrimidine ring system that carries an oxo group at the 7-position. 1,3-thiazolo[5,4-d]pyrimidine consists of a 1,3-thiazole ring fused to but not sharing a nitrogen atom with a pyrimidine ring.
Furo[2,3-c]pyridinesCHEMONTID:0004408Aromatic compounds containing a furopyridine ring system, where the O- and the N-atom are at the 1- and 6- position, respectively.
Furo[3,2-c]pyridinesCHEMONTID:0004409Aromatic compounds containing a furopyridine ring system, where the O- and the N-atom are at the 1- and 5- position, respectively.
Pyrrolo[2,3-d]pyrimidinesCHEMONTID:0004415Aromatic heteropolycyclic compounds containing a pyrrolo[2,3-d]pyrimidine ring system, which is an pyrrolopyrimidine isomers having the 3 ring nitrogen atoms at the 1-, 5-, and 7-positions.
Pyrido[2,3-d]pyrimidinesCHEMONTID:0004417Compounds containing the pyrido[2,3-d]pyrimidine ring system, which is a pyridopyrimidine isomer with three ring nitrogen atoms at the 1-, 3-, and 8- position.
Pyrrolo[2,1-f][1,2,4]triazinesCHEMONTID:0004418Aromatic heterocyclic compounds containing a pyrrolo[2,1-f][1,2,4]triazine ring system. Pyrrolo[2,1-f][1,2,4]triazine consists of a 1,2,4-triazine ring fused to and sharing the N2-atom with a pyrrole ring.
Pyrido[3,4-d]pyrimidinesCHEMONTID:0004419Compounds containing the pyrido[3,4-d]pyrimidine ring system, which is a pyridopyrimidine isomer with three ring nitrogen atoms at the 1-, 3-, and 7- position.
Benzo[c]quinolizin-3-onesCHEMONTID:0004422Aromatic organonitrogen heterocyclic compounds containing a benzo[c]quinolizine ring system, which carries an oxo group at the 3-position.
Dithiocarbamate saltsCHEMONTID:0004429Salts of dithiocarbamic acids.
Chloroformic acid estersCHEMONTID:0004430Organochlorine compounds which are esters of chloroformic acid.
Sulfonic acid estersCHEMONTID:0004435Esters of sulfonic acid, which have the general structure RS(=O)2OR' (R,R' = organyl group or H).
Organic sulfonic anhydridesCHEMONTID:0004437Organic compounds having the structure RS(=O)2OS(=O)2R', where R , R' = H or organyl group.
Organic sulfonic acidsCHEMONTID:0004438Organic compounds containing a sulfonic acid or derivative, with the general structure RS(=O)2OH (R= H or organyl group).
Organic sulfonamidesCHEMONTID:0004439Organic compounds containing the sulfonamide functional group, an amide of sulfonic acid with the general structure R1S(=O)2N(R2)R3 (R1=H or organyl; R2,R3=H, alkyl, aryl).
Transition metal alkylsCHEMONTID:0004443Metal alkyls, where the alkyl group is attached to a transition metal atom.
Carbonate saltsCHEMONTID:0004447Compounds that results from the interaction between a positive ion and the negatively charge oxygen atom of the carbonate ion.
Acrylic acids and derivativesCHEMONTID:0004450Organic compounds containing acrylic acid CH2=CHCO2H or a derivative thereof.
TriazolinesCHEMONTID:0004461Compounds that contain the triazoline ring, which is a five-membered unsaturated ring having two carbon atoms, three nitrogen atoms and one double bond.
OrganoazidesCHEMONTID:0004467Compounds bearing the group N3, viz. -N=N+=N- attached to an organic group.
Unsaturated aliphatic hydrocarbonsCHEMONTID:0004476Aliphatic Hydrocarbons that contains one or more unsaturated carbon atoms. These compounds contain one or more double or triple bonds.
Cyclohexyl halidesCHEMONTID:0004485Organohalogen compounds containing a monocyclic cyclohexane moiety that is substituted at one or more positions by an halogen atom.
Organic beryllium saltsCHEMONTID:0004489Organic compounds containing a beryllium ion.
Organic metal halidesCHEMONTID:0004491Organic compounds containing metals and halogens. Some are ionic while others are covalently bonded.
Organonickel compoundsCHEMONTID:0004492Organic compounds containing a bond between a carbon atom and a nickel atom.
Organic calcium saltsCHEMONTID:0004493Organic salts containing a calcium ion.
3',5'-cyclic purine nucleoside phosphorothioatesCHEMONTID:00044963',5'-cyclic purine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 3',5'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 3'- and 5'-positions of the ribose are part of the phosphorothioate group.
3',5'-cyclic pyrimidine nucleoside phosphorothioatesCHEMONTID:00044973',5'-cyclic pyrimidine nucleoside phosphate analogues, where a phosphate oxygen has been exchanged for sulphur generating a chiral phosphorothioate. In 3',5'-cyclic nucleoside phosphorothioate, the oxygen atoms at the 3'- and 5'-positions of the ribose are part of the phosphorothioate group.
5'-deoxy-5'-thionucleosidesCHEMONTID:00045035'-deoxyribonucleosides in which the ribose is thio-substituted at the 5'position by a S-alkyl group.
7-alkoxylcoumarinsCHEMONTID:0004510Aromatic heterocyclic compounds that contain a coumarin ring substituted at the 7-position by an alkoxy group.
Sulfonyl isocyanatesCHEMONTID:0004515Organosulfur compounds that contain a sulfonyl group connected to an isocyanate group.
Sulfonyl isothiocyanatesCHEMONTID:0004516Organosulfur compounds that contain a sulfonyl group connected to an isothiocyanate group.
4-quinolinemethanolsCHEMONTID:0004538Organoheterocyclic compounds containing a quinoline moiety substituted at the 4-position with a methanol.
Organothalium compoundsCHEMONTID:0004539Compounds containing a bond between a carbon atom and a thalium atom.
ArylhydroxamatesCHEMONTID:0004545Aromatic compounds containing an hydroxamate group attached to an aromatic moiety.
Benzyl isothiocyanatesCHEMONTID:0004548Aromatic compounds containing an isothiocyanate group that is N-substituted to a benzyl group.
Benzyl thiocyanatesCHEMONTID:0004549Aromatic compounds containing an thiocyanate group that is S-substituted to a benzyl group.
TrifluoromethylbenzenesCHEMONTID:0004551Organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups.
CumulenesCHEMONTID:0004553Hydrocarbons that contain at least three consecutive double bonds.
Metal acetylidesCHEMONTID:0004566Organic compounds containing an acetylide group substituted with a metal atom.
Acetylenic peroxidesCHEMONTID:0004567Organooxygen compounds with the general formula RC#CCOOH or RC#CCOO-.
Alkyl hydroperoxidesCHEMONTID:0004582Organooxygen compounds containing a hydroperoxide group substituted with an alkyl group. They have the general formula ROOH, where R is the alkyl group.
Allylic hydroperoxidesCHEMONTID:0004585Organooxygen compounds containing a hydroperoxide group substituted with an allyl group. They have the general formula RCH=CR'CH2OSO2CF3.
DiazoethersCHEMONTID:0004586Organooxygen compounds with the general formula RN=NOR' (R=H or organyl, R'=organyl).
Bis-arenediazo oxidesCHEMONTID:0004588Organonitrogen compounds with the general formula RN=NON=NR', where R and R' are aryl groups.
Bis-arenediazo sulfidesCHEMONTID:0004589Organonitrogen compounds with the general formula RN=NON=NR', where R and R' are aryl groups.
Arenediazo aryl sulfidesCHEMONTID:0004590Organonitrogen compounds with the general formula RN=NSR', where R,R' are aryl groups.
Organozinc compoundsCHEMONTID:0004592Organometallic compounds that contain a chemical bond between a carbon atom and a zinc atom.
3-cyanotriazenesCHEMONTID:0004599Organonitrogen compounds with the general formula NN=NC#N.
Dialkyl hyponitritesCHEMONTID:0004601Organooxygen compounds with the general structure is RON=NOR', where R and R' are alkyl groups.
Diazonium sulfatesCHEMONTID:0004604Organic mixtures of diazonium salts and sulfate salts. They have the general structure (RN+2 )2(SO4)2- , R'N+2 H(SO4)-, where R and R' are organyl groups.
Difluoroamino compoundsCHEMONTID:0004606Organonitrogen compounds containing an amine group substituted with two fluorine atoms, and an organyl group.
Metal thiocyanatesCHEMONTID:0004611Metal salts of thiocyanic acid.
Phenylboronic acidsCHEMONTID:0004615Aromatic compounds containing a monocyclic benzene ring that carries a boronic acid.
Branched unsaturated hydrocarbonsCHEMONTID:0004622Hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch.
4-alkoxyphenolsCHEMONTID:0004628Phenols that carry an alkoxy group at the 4-position of the benzene ring.
Benzyl sulfoxidesCHEMONTID:0004629Organosulfur compounds that contain a sulfoxide group substituted by a benzyl group. They have the general structure RS(=O)R' ( R=benzyl, R'=organyl).
Phenyl sulfoxidesCHEMONTID:0004632Organosulfur compounds containing a sulfoxide group substituted with a phenyl group.
Phenyl methylcarbamatesCHEMONTID:0004640Aromatic compounds containing a methylcarbamic acid esterified with a phenyl group.
Phenylacetic acid estersCHEMONTID:0004643Ester derivatives o phenylacetic acids.
1-hydroxy-2-unsubstituted benzenoidsCHEMONTID:0004646Phenols that a unsubstituted at the 2-position.
1-hydroxy-4-unsubstituted benzenoidsCHEMONTID:0004647Phenols that are unsubstituted at the 4-position.
N-alkyl-O-phenylhydroxylaminesCHEMONTID:0004652Hydroxylamines that are O-substituted with a phenyl group, and N-substituted by an alkyl group.
N-aryl-N-phenylhydroxylaminesCHEMONTID:0004653Hydroxylamines that are N,N-disubstituted by a phenyl and another aryl group.
Benzotriazine organothiophosphatesCHEMONTID:0004660Aromatic compounds containing a benzo-1,2,3-triazine, which is substituted by an organothiophosphate group at the 3-position. Their general structure is R-CSP(=S)(OR')OR'', where R=benzo-1,2,3-triazine, R',R\" = any atom.
Phosphoramidothioic acid S-estersCHEMONTID:0004663Organooxygen compounds containing a S-ester derivative of phosphoroamidothioic acid. They have the general structure RSP(=O)(O)(NH2), where R is an organyl group.
Phosphoramidothioic acid O-estersCHEMONTID:0004664Organooxygen compounds containing a O-ester derivative of phosphoroamidothioic acid. They have the general structure ROP(=O)(S)(NH2), where R is an organyl group.
Phosphoramidothioic-acid-O,S-diestersCHEMONTID:0004665Organooxygen compounds containing a O,S-diester derivative of phosphoroamidothioic acid. They have the general structure RSP(=O)(OR')(NH2), where R,R' are organyl groups.
Aminophenyl ethersCHEMONTID:0004670Aromatic compounds that contain a phenol ether, which carries an amine group on the benzene ring.
Benzofuranyl 5-alkylsulfonatesCHEMONTID:0004672Polycyclic aromatic compounds that contain a benzofuran ring system, which is O-substituted at the 5-position with an alkylsulfonate group.
2-phenoxypropionic acidsCHEMONTID:0004676Aromatic compounds hat contain a phenol ether attached to the C2-atom of a phenylpropionic acid.
2-phenoxypropionic acid estersCHEMONTID:0004677Aromatic compounds hat contain a phenol ether attached to the C2-atom of a phenylpropionic acid ester.
1,2,4-triazolopyrimidine-2-sulfonamidesCHEMONTID:0004681Polycyclic aromatic compounds containing a 1,2,4-triazolo[1,5-a]pyrimidine ring system, which is substituted with a sulfonamide at the 2-position.
IsothiosemicarbazonesCHEMONTID:0004693Organosulfur compounds NC(SR)=NN=C(R')R\", where R,R',R\" = H or organyl group.
1,4-dihydroxy-2-halobenzenoidsCHEMONTID:0004695Aromatic compounds containing a 1,-2-dihydroxybenzene moiety, which carries an halogen atom at the ring 2-position.
2-pyridylmethylaminesCHEMONTID:0004708Aromatic heterocyclic compounds contaning a pyridine ring which is substituted at the 2-position with a methylamine.
2-benzimidazolylcarbamic acidsCHEMONTID:0004710Aromatic heteropolycyclic compounds that contain a carbamyl group N-linked to the C2-atom of a benzimidazole moiety.
2-benzimidazolylcarbamic acid estersCHEMONTID:0004711Aromatic heteropolycyclic compounds that contain a carbamic acid ester group, which is N-linked to the C2-atom of a benzimidazole moiety.
Phenylcarbamic acid estersCHEMONTID:0004714Ester derivatives of phenylcarbamic acids.
Formamidine disulfidesCHEMONTID:0004730Organonitrogen compounds containing the compound H2NC(=NH)SSC(=NH)NH2 and its derivatives formed by substitution at nitrogen.
1,2,3-oxadiazinesCHEMONTID:0004737Heterocyclic compounds containig an oxadiazine ring with one oxygen atom at the 1-position, and two nitrogen atoms at the 2-, and 3-position, respectively.
1,2,4-oxadiazinesCHEMONTID:0004738Heterocyclic compounds containig an oxadiazine ring with one oxygen atom at the 1-position, and two nitrogen atoms at the 2-, and 4-position, respectively.
1,2,5-oxadiazinesCHEMONTID:0004739Heterocyclic compounds containig an oxadiazine ring with one oxygen atom at the 1-position, and two nitrogen atoms at the 2-, and 5-position, respectively.
1,3,4-oxadiazinesCHEMONTID:0004740Heterocyclic compounds containig an oxadiazine ring with one oxygen atom at the 1-position, and two nitrogen atoms at the 3-, and 4-position, respectively.
1,3,5-oxadiazinesCHEMONTID:0004741Heterocyclic compounds containig an oxadiazine ring with one oxygen atom at the 1-position, and two nitrogen atoms at the 3-, and 5-position, respectively.
Phenoxy compoundsCHEMONTID:0004742Aromatic compounds contaning a phenoxy group.
3-phenoxypropionic acidsCHEMONTID:0004743Aromatic compounds containing a 3-phenoxypropionic acid.
Oxime carbamatesCHEMONTID:0004752Oxime ether derivatives with the general formula CC(R)=NOC(=O)N(R')R\", where R-R\" = H or organyl.
7-benzofuranyl methylcarbamatesCHEMONTID:0004764Aromatic heteropolycyclic compounds containing a 1-benzofuran moiety, that is O-substituted with a N-methylcarbamate at the 7-position.
Oxime organothiophosphatesCHEMONTID:0004765Organic compounds containing an oxime group, which is O-substituted with a thiophosphoric acid ester.
PhenylphosphonothioatesCHEMONTID:0004766Aromatic compound contaning a phosphonothioate, which is C-substituted with a phenyl group.
Sulfonated stilbenesCHEMONTID:0004785Stilbenes that carry a sulfone group at one or more positions of either benzene rings.
FuranonaphthodioxolesCHEMONTID:0004792Aromatic heterocyclic compounds containing a 1,3-dioxole ring linearly fused to the a naphthofuran.
Dithiophosphate S,S-diestersCHEMONTID:0004793Organic compound containing a S,S-diester derivative of dithiophosphoric acid.
ChloronaphthalenesCHEMONTID:0004794Aromatic heterocyclic compounds containing a naphthalene moiety substituted at one or more positions by a chlorine atom.
5'-azido-5'-deoxyribonucleosidesCHEMONTID:0004801A 5'-deoxyribonucleoside where the 5'-hydroxy group of the sugar moiety is substituted by a methylsulfanyl group.
Organic dichromatesCHEMONTID:0004803Organic compounds containing a dichromate moiety.
AlkoxidesCHEMONTID:0004806Organooxygen compounds with the general structure RO-, where R is an alkyl group.
EcdysteroidsCHEMONTID:0004813Polyhydroxylated oxosteroids possessing a cyclopentano-perhydro-phenantrene with beta side-chain at C-17, which is the product of terpene biosynthesis through mevalonic acid, cholesterol and related sterols. Ecdysteroids are found in certain plants and animals.
Organic chromium trioxidesCHEMONTID:0004820Organic compounds containing a chromium trioxide moiety.
C8-prenylated coumarinsCHEMONTID:0004821Aromatic compounds containing a coumarin skeleton, which is substituted by a prenyl group at the C8-position.
4-hydroxy-6,7-benzomorphansCHEMONTID:0004822Aromatic heteropolycyclic compounds containing a 6,7-benzomorphan skeleton, which is hydroxylated at the ring 4-position.
2,6-dimethyl-3-benzazocinesCHEMONTID:0004823Aromatic compounds containing a 6,7-benzomorphan skeleton, which is substituted by methyl group at the 2- and 6-positions.
PyridinolatesCHEMONTID:0004825Aromatic compounds similar to phenoxide, with the difference that one carbo atom of the benzene ring is replaced by a nitrogen compound.
Pyrroloquinoline quinonesCHEMONTID:0000005Compounds with a structure based on the 2,7,-tricarboxy-1H-pyrrolo[2,3-f ]quinoline-4,5-dione. Pyrroloquinoline Quinones usually bear a carboxylic acid group at the C-2, C-7 and C-9 positions.
Cembrane diterpenoidsCHEMONTID:0000008Diterpenoids with a structure based a cembrane skeleton, which is characterized by the presence of an isopropyl group at C-1 and by three symmetrically disposed methyl groups a the t C-4, -8 and -12 positions.
Cyclic olefinsCHEMONTID:0002840Olefins that contain at least one ring in their structure.
Purine ribonucleoside bisphosphatesCHEMONTID:0000026Purine Ribonucleotides in which the ribose sugar esterified with one phosphate group attached to each of two different hydroxy groups on the sugar, usually at positions 2', 3', or 5'.
Pyridoxals and derivativesCHEMONTID:0000028Compounds containing a pyridoxal moiety, which consists of a pyridine ring substituted at positions 2,3,4, and 5 by a methyl group, a hydroxyl group, a carbaldehyde group, and a hydroxymethyl group, respectively.
Hydroxyeicosatrienoic acidsCHEMONTID:0000030Eicosanoic acids with an attached hydroxyl group and three CC double bonds.
Sulfobenzoic acidsCHEMONTID:0000034Benzoic acids carrying a sulfonyl group on the benzene ring.
IndanedionesCHEMONTID:0000040Compounds containing an indane ring bearing two ketone groups.
BiphenylbenzimidazolesCHEMONTID:0000043Organic compounds containing a biphenyl attached to a benzimidazole. A carbon atom of the biphenyl moiety is boned to a carbon or the nitrogen atom of the benzimidazole moiety.
Phenyltetrazoles and derivativesCHEMONTID:0000306Compounds containing a phenyltetrazole skeleton, which consists of a tetrazole bound to a phenyl group.
Hydroxyeicosatetraenoic acidsCHEMONTID:0000046Eicosanoic acids with an attached hydroxyl group and four CC double bonds.
Aromatic monoterpenoidsCHEMONTID:0000051Monoterpenoids containing at least one aromatic ring.
Brominated biphenylsCHEMONTID:0000052Organic compounds containing a biphenyl moiety substituted at one or more positions by a bromine atom.
Coumaric acids and derivativesCHEMONTID:0000059Aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.
Amino acids and derivativesCHEMONTID:0000347Organic compounds containing an amine group, a carboxylic acid group (or a derivative thereof), and a side-chain that is specific to each amino acid.
Sulfanylbenzoic acids and derivativesCHEMONTID:0002086Benzoic acids (or derivatives) which bear a sulfanyl group (R-SH) attached to the benzene ring.
Phenanthridines and derivativesCHEMONTID:0000100Polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included.
Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoidsCHEMONTID:0000101Sesquiterpenoids with a structure based on the eudesmane skeleton.
SemicarbazidesCHEMONTID:0000114Organic compounds containing the semicarbazide functional group with the general structure R1(N)R2NR3C(=O)N(R4)R5 (R1-R5=H, alkyl, aryl), a derivative of urea, where the amine group on one side has been replace by a hydrazine group.
HydrazonesCHEMONTID:0000116Compounds containing an N-Alkylidene derivative of hydrazine. They have the generic structure RNN=C(R')R\" (R,R',R\"= H or organyl group).
KetonesCHEMONTID:0000118Organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.
AldehydesCHEMONTID:0000124Organic compounds containing the aldehyde functional group.
Alkyl aryl ethersCHEMONTID:0000128Organic compounds containing the alkyl aryl ether functional group with the generic formula R-O-R' , where R is an alkyl group and R' is an aryl group.
1,3-dicarbonyl compoundsCHEMONTID:0000133Carbonyl compounds with the generic formula O=C(R)C(H)C(R')=O, where R and R' can be any group.
CatecholsCHEMONTID:0000135Compounds containing a 1,2-benzenediol moiety.
HydroquinonesCHEMONTID:0000136Compounds containing a hydroquinone moiety, which consists of a benzene ring with a hydroxyl groups at positions 1 and 4.
ResorcinolsCHEMONTID:0000137Compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.
BisphenolsCHEMONTID:0000143Organic compounds containing two hydroxyphenyl group based on a diphenylmethane backbone.
ChromonesCHEMONTID:0000144Compounds containing a benzopyran-4-one moiety.
Angular furanocoumarinsCHEMONTID:0002568Furanocoumarins, with a structure characterized by a furan ring angularly fused to a coumarin.
CarbapenemsCHEMONTID:0000167Beta-lactam derivatives in which the beta-lactam ring shares the nitrogen atom with a pyrrole-2-carboxylic acid.
CephemsCHEMONTID:0000168Organic compounds containing the 5-thia-1-azabicyclo[4.2.0]oct-2-en-8-one nucleus.
ClavamsCHEMONTID:0000169Organic compounds containing a 4-oxa-1-azabicyclo[3.2.0]heptan-7-one moiety. Clavams are similar to penams, but with an oxygen substituted for the sulfur in the penam skeleton.
MonobactamsCHEMONTID:0000170Compounds comprising beta-lactam ring is alone and not fused to another ring.
OxacephemsCHEMONTID:0000171Organic compounds containing the oxacepehem skeleton, which is similar to a cephem, but with oxygen substituted for the sulfur.
PenamsCHEMONTID:0000172Organic heterocyclic compounds containing the 4-thia-1-azabicyclo[3.2.0]heptan-7-one structure.
BenzamidesCHEMONTID:0000178Organic compounds containing a carboxamido substituent attached to a benzene ring.
Oleanane triterpenoidsCHEMONTID:0000180Triterpenoids with a structure based on the oleanane skeleton, an 4,4,6a,8a,11,14b-heptamethyl-hexadecahydropicene derivative.
Amphetamines and derivativesCHEMONTID:0000188Organic compounds containing or derived from 1-phenylpropan-2-amine.
OxazolidinonesCHEMONTID:0000196Compounds containing an oxazolidinone moiety, which is an oxazolidine bearing a ketone group.
OligosaccharidesCHEMONTID:0000198Carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.
ThioxanthenesCHEMONTID:0000199Organic polycyclic compounds containing a thioxanthene moiety, which is an aromatic tricycle derived from xanthene by replacing the oxygen atom with a sulfur atom.
DibenzopyransCHEMONTID:0002817Organic heterocyclic compounds with a structure containing a dibenzopyran moiety, made up of two benzene rings fused to a central pyran ring.
Vitamin E compoundsCHEMONTID:0001546A group of fat-soluble compounds containing or derived either from a tocopherol or a tocotrienol skeleton.
Linear furanocoumarinsCHEMONTID:0002569Furanocoumarins, with a structure characterized by a furan ring linearly fused to a coumarin.
PyrazolonesCHEMONTID:0000205Compounds containing a pyrazole ring which bears a ketone.
CinnolinesCHEMONTID:0000206Organic aromatic compounds containing a benzene fused to a pyridazine ring.
PhthalazinesCHEMONTID:0000207Compounds containing a phthalazine moiety, which consists of a benzene ring fused to a pyridazine, forming a 2,3-benzodiazine skeleton.
PyridazinonesCHEMONTID:0000208Compounds containing a pyridazine ring which bears a ketone.
Hydroxyeicosapentaenoic acidsCHEMONTID:0000214Eicosanoic acids with an attached hydroxyl group and five CC double bonds.
Sugar acids and derivativesCHEMONTID:0000215Compounds containing a saccharide unit which bears a carboxylic acid group.
NitrothiazolesCHEMONTID:0000225Compounds containing a thiazole ring which bears a nitro group.
ThiazolidinonesCHEMONTID:0000227Heterocyclic compounds containing a thiazolidinone ring which bears one ketone group.
TriazolonesCHEMONTID:0000234Compounds containing a triazole ring which bears a ketone group.
Acyl phosphatesCHEMONTID:0004781Organic compounds containing a phosphate linked to an acyl group. They have the general structure R-CO-P(O)(O)O, R=H or organyl.
PyranoindolizinesCHEMONTID:0000241Polycyclic aromatic compounds containing a pyran ring fused to an indolizine moiety.
Substituted imidazolesCHEMONTID:0002310Heterocyclic compounds containing an imidazole ring substituted at one or more positions.
PurinonesCHEMONTID:0000597Purines in which the purine moiety bears a C=O group. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
XanthinesCHEMONTID:0000247Purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety.
ThioxanthinesCHEMONTID:0000249Organic polycyclic compounds containing a thioxanthine moiety, which is an aromatic bicyclic structure derived from xanthine by replacing a carbonyl group with a thiocarbonyl group.
Pteroic acids and derivativesCHEMONTID:0001228Compounds that are composed of a pterin with a 4-aminobenzoic acid (or a derivative) at the 6 position on the pteridine ring. Pteridine is a ring system made up of a pyrazine fused to a pyrimidine.
Hydroxy bile acids, alcohols and derivativesCHEMONTID:0002194Bile acids, alcohols or derivatives bearing at least hydroxyl group.
Sesquiterpene glycosidesCHEMONTID:0000263Sesquiterpenoids linked to a saccharide moiety through a glycosidic bond.
Miscellaneous chromatesCHEMONTID:0000273Inorganic compounds in which the largest metallic oxoanion is chromate, to which either no atom or a non metal atom is bonded.
AcridinesCHEMONTID:0000274Organic compounds containing the acridine moiety, a linear tricyclic heterocycle which consists of two benzene rings joined by a pyridine ring.
Aminobenzoic acids and derivativesCHEMONTID:0000281Benzoic acids (or derivative thereof) containing an amine group attached to the benzene moiety.
AminosaccharidesCHEMONTID:0003305Saccharides containing a sugar unit that bears an amino group.
Primary alcoholsCHEMONTID:0000286Compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).
PyrimidonesCHEMONTID:0000291Compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
LysophosphatidylglycerolsCHEMONTID:0000297Glycerophosphoglycerols (molecules containing a glycerol moiety attached to the phosphate group linked to a glycerol) in which only one fatty acid is bonded to the 1-glycerol moiety (through an ester linkage).
PhosphatidylglycerophosphatesCHEMONTID:0000332Glycerophosphoglycerophosphates in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages.
Straight chain fatty acidsCHEMONTID:0000333Fatty acids with a straight aliphatic chain.
Branched fatty acidsCHEMONTID:0000338Fatty acids containing a branched chain.
Unsaturated fatty acidsCHEMONTID:0000339Fatty acids with a chain that contains at least one CC double bond.
Hydroperoxy fatty acidsCHEMONTID:0000340Fatty acids containing a hydroperoxide group attached to the chain.
Hydroxy fatty acidsCHEMONTID:0000341Fatty acids in which the chain bears a hydroxyl group.
PyridinylpyrimidinesCHEMONTID:0000342Compounds containing a pyridinylpyrimidine skeleton, which consists of a pyridine linked (not fused) to a pyrimidine by a bond.
PeptidesCHEMONTID:0000348Compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.
Biflorane and serrulatane diterpenoidsCHEMONTID:0000351Diterpenoids with a structure based either on the biflorane or the serrulatane skeleton.
Cobalamin derivativesCHEMONTID:0000352Organic compounds containing a corrin ring, a cobalt atom, an a nucleotide moiety. Cobalamin Derivatives are actually derived from vitamin B12.
CurcuminoidsCHEMONTID:0000356Aromatic compounds containing a curcumin moiety, which is composed of two aryl buten-2-one (feruloyl) chromophores joined by a methylene group.
NitrilesCHEMONTID:0000362Compounds having the structure RC#N; thus C-substituted derivatives of hydrocyanic acid, HC#N.
Organic N-nitroso compoundsCHEMONTID:0004777Organic compounds containing a n-nitroso group -NN=O.
DihydropyridinesCHEMONTID:0000367Compounds containing a dihydropyridine moiety, which is a semi-saturated pyridine derivative with two double bonds.
PhenylmorpholinesCHEMONTID:0000370Aromatic compounds containing a morpholine ring and a benzene ring linked to each other through a CC or a CN bond.
ErgopeptinesCHEMONTID:0002030Ergoline derivatives that contain a tripeptide structure attached to the basic ergoline ring in the same location as the amide group of the lysergic acid derivatives.
Hydroxyquinols and derivativesCHEMONTID:0000380Compounds containing a 1,2,4-trihydroxybenzene moiety.
Phloroglucinols and derivativesCHEMONTID:0000382Compounds containing a phloroglucinol (benzene-1,3,5-triol) moiety, which consists of a benzene ring bearing one hydroxyl group at positions 1,3, and 5.
Hydroperoxyeicosatrienoic acidsCHEMONTID:0000383Eicosanoic acids with an attached hydroperoxyl group and three CC double bonds.
Batrachotoxins and derivativesCHEMONTID:0000385Potent cardiotoxic and neurotoxic alkaloids containing a C21-steroid backbone. They have been characterized from skin extracts of different frog species. The batrachotoxins have a homomorpholine ring at the steroidal CD-ring junction, a 3,9-hemiketal bridge and, in some cases, a 20beta-2,4-dialkylpyrrole-3-carboxylate moiety.
CholinesCHEMONTID:0001012Organic compounds containing a N,N,N-trimethylethanolammonium cation.
Hydroperoxyeicosatetraenoic acidsCHEMONTID:0000387Eicosanoic acids with an attached hydroperoxyl group and four CC double bonds.
Mitomycins, mitosane and mitosene derivativesCHEMONTID:0004096A group of pyrroloindolediones, which carry a methyl group at the 6-position of their quinone moiety. The mitosane (containing an aziridine) and mitosene server as backbone for mitomycins and their derivatives.
Oxoeicosapolyenoic acidsCHEMONTID:0000393Eicosapolyenoic acids (C20 fatty acid with more than one C=C double bonds on the chain).
Pyrogallols and derivativesCHEMONTID:0000397Compounds containing a 1,2,3-trihydroxybenzene moiety.
Miscellaneous chromitesCHEMONTID:0000404Inorganic compounds in which the largest metallic oxoanion is chromite, to which either no atom or a non metal atom is bonded.
Keto fatty acidsCHEMONTID:0000409Fatty acids containing a ketone group attached to the acyl chain.
QuinoxalinesCHEMONTID:0000486Compounds containing a quinoxaline moiety, a bicyclic heterocycle made up of a benzene ring fused to a pyrazine ring.
Dibenzo-p-dioxinsCHEMONTID:0001381Compounds containing a dibenzo-p-dioxin moiety, which consists of two benzene connected by a para-dioxin ring.
Methoxy fatty acidsCHEMONTID:0000421Lipids containing a methoxy group linked to a fatty acid chain.
MetalloporphyrinsCHEMONTID:0000452Polycyclic compounds containing a porphyrin moiety and a metal atom.
Hydroxycinnamic acid estersCHEMONTID:0003002Ester derivatives of hydroxycinnamic acids.
Carboxylic acid anhydridesCHEMONTID:0001240Carboxylic acid derivatives two carbonyl groups where the carbon atoms are both linked to the same oxygen atom.
Primary aminesCHEMONTID:0002450Amines having the nitrogen atom linked to exactly one hydrocarbyl group.
EnaminesCHEMONTID:0000470Compounds containing the enamine functional group with the general structure R1N(R2)CR=C(R3)R4.
Nitro fatty acidsCHEMONTID:0000471Fatty acids containing a nitro group.
BiguanidesCHEMONTID:0000474Organic compounds containing two N-linked guanidines.
Carboxylic acid amidesCHEMONTID:0000475Carboxylic acid derivatives containing a carbonyl group in which the carbon atom is linked to a nitrogen atom (substituted or not). The general formula of the carboxylic acid amide is R1C(=O)N(R2)R3 (R1,R2,R3=H, alkyl, aryl).
Acyclic sesquiterpenoidsCHEMONTID:0000477Sesquiterpenoids (compounds made of three consecutive isoprene units) that do not contain a cycle.
Polyprenyl phosphatesCHEMONTID:0000478Prenol lipids in which the phosphate group is linked to one end of the polyprenol moiety.
Halogenated fatty acidsCHEMONTID:0000483Fatty acids with a chain that carries a halogen atom (Cl,F,I,Br).
QuinazolinesCHEMONTID:0000485Compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.
Hydroxybenzoic acid derivativesCHEMONTID:0001248Compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.
Amino fatty acidsCHEMONTID:0000489Fatty acids containing an amine group.
IsoflavonesCHEMONTID:0000494Polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom.
Carbocyclic fatty acidsCHEMONTID:0000495Fatty acids containing a carbocyclic ring .
Amine oxides and derivativesCHEMONTID:0000496Organic compounds that contains the amine oxide functional group with the formula R3N+-O-, which substituted by at least one organic group.
Chlorinated biphenylsCHEMONTID:0000500Organic compounds containing at least one chlorine atom attached to either benzene ring of the biphenyl moiety.
Sesquiterpene lactonesCHEMONTID:0001543Sesquiterpenoids containing a lactone ring.
12-oxophytodienoic acid metabolitesCHEMONTID:0000511Biologically active organic compounds containing 12-oxophytodienoic acid, which consists of an oxo-cyclopentene linked to both an octanoic acid chain and pentene chain.
Jasmonic acidsCHEMONTID:0000512Lipids containing or derived from a jasmonic acid, with a structure characterized by the presence of an alkene chain linked to a 2-(3-oxocyclopentyl)acetic acid moiety.
Prostaglandins and related compoundsCHEMONTID:0000514Unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.
LeukotrienesCHEMONTID:0000515Eicosanoids containing a hydroxyl group attached to the aliphatic chain of an arachidonic acid. Leukotrienes have four double bonds, three (and only three) of which are conjugated.
ThromboxanesCHEMONTID:0000519Eicosanoids structurally characterized by the presence of a 6-member ether containing ring.
N,N-diphenylcarbamic acidsCHEMONTID:0000623Compounds containing two phenyl groups linked to the nitrogen atom of a carbamic acid.
Taxanes and derivativesCHEMONTID:0000676Diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] propellane ring system.
Sesterterpene lactonesCHEMONTID:0000702Sesterterpenoids containing a lactone ring.
Enol ethersCHEMONTID:0001009Compounds containing the enol ether functional group, with the formula R3OCR2=CR1.
Oxime ethersCHEMONTID:0001010Compounds containing the oxime ether functional group, with the general structure R1(R2)C=NOR3 ( R3 not H).
Hydroperoxyeicosapentaenoic acidsCHEMONTID:0001011Eicosanoic acids with an attached hydroperoxyl group and five CC double bonds.
Epoxyeicosatrienoic acidsCHEMONTID:0001015Eicosatrienoic acids containing an oxirane ring as part of its aliphatic chain.
Acyclic olefinsCHEMONTID:0002839Olefins that do not contain a ring in their structure.
HepoxilinsCHEMONTID:0001020Eicosanoids containing an oxirane group attached to the fatty acyl chain.
Clavulones and derivativesCHEMONTID:0001021Ester derivatives of prostanoids.
CarboxamidinesCHEMONTID:0001045Carboxylic acid derivatives containing the amidine group.
SulfinamidinesCHEMONTID:0001046Compounds containing a sulfinamidine group, with the general structure RS(=NR)NR2.
PhosphinamidinesCHEMONTID:0001047Compounds containing a phosphinamidine group, with the general structure R2P(=NR)NR2.
DithiazolethionesCHEMONTID:0001128Compounds containing a dithiazole bearing a thioketone group.
AlkanolaminesCHEMONTID:0002460Organic compounds that carry a hydroxy and an amino functional groups on an alkane backbone.
Neutral glycosphingolipidsCHEMONTID:0001419Glycosphingolipids in which the ceramide skeleton is bound to an oligosaccharide (usually 3 to 5 units) moiety made up of a glucose (as primary unit bound to the ceramide moiety) and galactose (Gal), N-acetylglucosamine (GlcNAc), N-acetylgalactosamine (GalNAc) or mannose (Man) as the other monosaccharides.
Acyl CoAsCHEMONTID:0001090Organic compounds containing a coenzyme A substructure linked to an acyl chain.
HemiacetalsCHEMONTID:0001092Compounds comprising the hemiacetal functional group, with the general formula R2C(OH)OR' ( R' not Hydrogen ).
Acyl carnitinesCHEMONTID:0001095Organic compounds containing a fatty acid with the carboxylic acid attached to carnitine through an ester bond.
N-acyl aminesCHEMONTID:0001096Compounds containing a fatty acid moiety linked to an amine group through an ester linkage.
BromobenzenesCHEMONTID:0001098Organic compounds containing a bromine atom attached to a benzene ring.
ChlorobenzenesCHEMONTID:0001099Compounds containing one or more chlorine atoms attached to a benzene moiety.
FluorobenzenesCHEMONTID:0001100Compounds containing one or more fluorine atoms attached to a benzene ring.
IodobenzenesCHEMONTID:0001101Aromatic compounds containing one or more iodine atoms attached to a benzene.
Acyl homoserine lactonesCHEMONTID:0001102N-acyl-homoserine-lactones attached to a long aliphatic chain.
Phthalic acid and derivativesCHEMONTID:0001105Compounds containing a phthalic acid moiety (or a derivative thereof), which is a benzene ring bearing a carboxylic acid group at two different ring positions. Isomers of phthalic acid include meta-phthalic acid (benzene-1,3-dioic acid), ortho-phthalic acid (benzene-1,2-dioic acid), and para-phthalic acid (benzene-1,4-dioic acid).
Phthalic anhydridesCHEMONTID:0001109Compounds containing a phthalic anhydride moiety (or a derivative thereof), which consists of a benzene fused to a furan-1,3-dione.
Polyprenyl phospho carbohydratesCHEMONTID:0001117Polyprenyl phosphates with a carbohydrate moiety attached to it.
Sulfonyl-1,2,3-triazolesCHEMONTID:0001119Cyclic compounds containing a sulfonyl group attached to a 1,2,3-triazole ring.
Sulfonyl-1,2,4-triazolesCHEMONTID:0001120Cyclic compounds containing a sulfonyl group attached to a 1,2,4-triazole ring.
Glycinated bile acids and derivativesCHEMONTID:0001124Compounds with a structure characterized by the presence of a glycine linked to a bile acid skeleton.
2,3-diphenylfuransCHEMONTID:0001126Organic heterocyclic compounds that contain a furan ring substituted with a phenyl group only the C2- and C3-positions.
Acyclic monoterpenoidsCHEMONTID:0001127Monoterpenes that do not contain a cycle.
DiacylglycerolsCHEMONTID:0001129Glycerides consisting of two fatty acid chains covalently bonded to a glycerol molecule through ester linkages.
SphingomyelinsCHEMONTID:0001131Sphingolipids containing a backbone formed of an alcohol - sphingosine, a phosphate group, a choline and fatty acid chain.
MonoacylglycerolsCHEMONTID:0001133Glycerides consisting of one fatty acid chain covalently bonded to a glycerol molecule through an ester linkage.
TriacylglycerolsCHEMONTID:0001135Glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.
FlavonolsCHEMONTID:0001136Compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position.
LeucoanthocyanidinsCHEMONTID:0001138Flavonoids consisting of a flavan (3,4-dihydro-2-phenyl-2H-1-benzopyran) moiety that carries two hydroxy groups at the C3- and C4-positions.
Phosphatidylinositol phosphatesCHEMONTID:0001139Phosphorylated derivatives of phosphatidylinositols, which are glycerophosphoinositols where the glycerol is esterified with two fatty acids.
SulfonylanilinesCHEMONTID:0001141Compounds containing an aniline moiety, which is para-substituted by a sulfonyl group.
FluoroquinolonesCHEMONTID:0001144Compounds containing a fluorine atom attached to a quinolone. Quinolone or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine, and bears a ketone group.
Sphaeroane diterpenoidsCHEMONTID:0001147Diterpenoids with a structure based on the 3a,6,9-trimethyl-3-(propan-2-yl)-tetradecahydrocyclohexa[e]azulene skeleton or formally 2,7-cyclodolabellane.
ImidazolidinonesCHEMONTID:0001149Organic compounds containing an imidazolidinone moiety, which is an imidazolidine ring bearing a ketone.
Taurinated bile acids and derivativesCHEMONTID:0001159Bile acid derivatives containing a taurine conjugated to the bile acid moiety.
PyridinonesCHEMONTID:0001160Compounds containing a pyridine ring, which bears a ketone.
Carboxylic acid hydrazidesCHEMONTID:0001165Carboxylic acid derivatives containing a carbonyl group in which the carbon is directly linked to a hydrazide group (N-N).
Carboxylic acid saltsCHEMONTID:0001166Ionic derivatives of carboxylic acid.
Dialkyl ethersCHEMONTID:0001167Organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
Organosulfonic acid estersCHEMONTID:0001178Esters of sulfonic acid, which have the general structure RS(=O)2OR' (R,R' = organyl, not H).
Organosulfonic acidsCHEMONTID:0001179Compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom).
Sulfuric acid diestersCHEMONTID:0001184Organic compounds containing the sulfuric acid diester functional group with the generic structure ROS(OR')(=O)=O, (R,R'=organyl group).
Sulfuric acid monoestersCHEMONTID:0001185Organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group).
Thiocarbamic acid estersCHEMONTID:0001190Organic compounds containing a functional group with the general structure R1OC(=S)N(R2)R3 (R1=alkyl, aryl; R2,R3=H, alkyl, aryl).
Thiocarbamic acid halidesCHEMONTID:0001191Organic compounds containing a functional group with the general structure R1C(=S)N(R2)R3 (R1=halogen; R2,R3=H, alkyl, aryl).
Organic thiocarbonic acidsCHEMONTID:0001193Organic compounds comprising the thiocarbonic acid group, with the general structure HOC(=S)OH.
Thiocarbonic acid ester halidesCHEMONTID:0001195Organic compounds containing a diester derivative of thiocarbonic acid, with the general formula XOC(=S)OR (X=F, I, Cl, Br; R=alkyl, aryl).
Thiocarbonic acid monoestersCHEMONTID:0001196Organic compounds containing a monoester derivative of thiocarbonic acid, with the general formula HOC(=S)OR (R=alkyl, aryl).
Thiocarbonic acid diestersCHEMONTID:0001197Organic compounds containing a diester derivative of thiocarbonic acid, with the general formula ROC(=S)OR' (R,R'=alkyl, aryl).
ThiosemicarbazidesCHEMONTID:0001207Compounds containing a derivative of thiosemicarbazide with the general structure R1N(R2)N(R3)C(=S)N(R4)R5 (R1-R5=H, alkyl, aryl) where the ketone group has carbonyl group has been replaced with a thiocarbonyl group.
YnaminesCHEMONTID:0001210N,N-Disubstituted alk-1-yn-1-amines RC≡CNR2.
DihydropyranonesCHEMONTID:0001211Compounds containing a hydrogenated pyran ring which bears a ketone, and contains one double bond.
DiarylethersCHEMONTID:0002463Organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.
PrecorrinsCHEMONTID:0001221Intermediates formed by methylation at one or more of the four rings prior to the formation of the macrocyclic corrin ring.
NitrosoureasCHEMONTID:0001229Compounds containing a nitro group and an urea group N-N linked together, with the general structure R1N(R2)C(=O)N(R3)N=O.
IsoureasCHEMONTID:0001231Organic compounds containing the isourea group, with the general structure R1N(R2)C(=NR3)OR4, or its hydrocarbyl derivatives (R1,R2,R3,R4=H, alkyl, aryl).
CardiolipinsCHEMONTID:0001233Glycerophospholipids in which the O1 and O3 oxygen atoms of the central glycerol moiety are each linked to one 1,2-diacylglycerol chain. Their general formula is OC(COP(O)(=O)OC[C@@H](CO[R1])O[R2])COP(O)(=O)OC[C@@H](CO[R3])O[R4], where R1-R4 are four fatty acyl chains.
Carboxylic acid estersCHEMONTID:0001238Carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
Carboxylic acid azidesCHEMONTID:0001239Carboxylic acid derivatives a carbonyl group in which the carbon is directly linked to an azide group (-N=N+=N-).
PhenylthiazolesCHEMONTID:0001242Compounds containing a phenylthiazole moiety, which consists of an thiazole ring attached to a phenyl group.
FlavinsCHEMONTID:0001249Compounds containing a flavin (7,8-dimethyl-benzo[g]pteridine-2,4-dione) moiety, with a structure characterized by an isoalloaxzine tricyclic ring.
Indole-3-acetic acid derivativesCHEMONTID:0001252Compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole.
1Z-alkenylglycero-3-phosphatesCHEMONTID:0001254Compounds containing glycerophosphate moiety attached to a 1-alkenyl group.
CDP-diacylglycerolsCHEMONTID:0001256Glycerolipids containing a diacylglycerol, with a cytidine diphosphate attached to the oxygen O1 or O2 of the glycerol part.
Aminopyrimidines and derivativesCHEMONTID:0001262Organic compounds containing an amino group attached to a pyrimidine ring. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
CDP-monoacylglycerolsCHEMONTID:0001264Glycerolipids containing a monoacylglycerol, with a cytidine diphosphate attached to the oxygen O1 or O2 of the glycerol part.
PhosphoethanolaminesCHEMONTID:0001266Compounds containing a phosphate linked to the second carbon of an ethanolamine.
AldiminesCHEMONTID:0001267Organic compounds containing the aldimine functional group.
Thiodiacetic acid derivativesCHEMONTID:0001271Compounds containing a thiodiacetic acid group (or esters/salts thereof) which is made up of two 2-sulfanylacetic (OC(=O)CS) acid moieties sharing their sulfur atom.
Meta cresolsCHEMONTID:0001273Aromatic compounds containing a meta-cresol moiety, which consists of a benzene ring bearing a methyl group and a hydroxyl group at ring positions 1 and 3, respectively.
Ortho cresolsCHEMONTID:0001274Organic compounds containing an ortho-cresol moiety, which consists of a benzene bearing one hydroxyl group at ring positions 1 and 2, respectively.
Para cresolsCHEMONTID:0001275Compounds containing a para cresol moiety, which consists of a benzene ring bearing one hydroxyl group at ring positions 1 and 4.
CarotenoidsCHEMONTID:0001277Organic compounds formed by eight consecutive isoprene fragments. Carotenoids are a subgroup of tetraterpenes, and are subdivided in two categories: Carotenes and Xanthophylls.
Decamethonium compoundsCHEMONTID:0001281Quaternary ammonium compounds containing a trimethyl-(10-trimethylammoniodecyl)ammonium moiety.
Hexamethonium compoundsCHEMONTID:0001282Organic compounds containing a N,N,N,N',N',N'-hexamethylhexane-1,6-diaminium moiety.
StrigolactonesCHEMONTID:0001284Terpene lactones structurally characterized by the presence of an indeno[1,2-b]furan and a 2,5-dihydrofuran-2-one linked together to form a 3-methyl-5-{8-methyl-2-oxo-indeno[1,2-b]furan-3-ylidene]methoxy}-2,5-dihydrofuran-2-one skeleton.
ThiaminesCHEMONTID:0001285Compounds containing a thiamine moiety, which is structurally characterized by a 3-[(4-Amino-2-methyl-pyrimidin-5-yl)methyl]-4-methyl-thiazol-5-yl backbone.
DialkylglycerophosphatesCHEMONTID:0001288Glycerophosphates in which the glycerol moiety is bonded to two aliphatic (saturated or unsaturated) chains through ether linkages.
Dialkylglycerol-3-phosphocholinesCHEMONTID:0001289Glycerophosphocholines in which the glycerol moiety is bonded to two aliphatic (saturated or unsaturated) chains through ether linkages.
PyranoquinolinesCHEMONTID:0001291Polycyclic compounds containing a pyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.
Cyclic alcohols and derivativesCHEMONTID:0001292Organic compounds containing an aliphatic ring substituted with at least one hydroxyl group.
PrenylquinonesCHEMONTID:0002802Quinones with a structure characterized by the quinone ring substituted by an prenyl side-chain.
1-acyl,2-alkylglycerophosphoglycerolsCHEMONTID:0001298Glycerophosphoglycerols that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O1-position, and one acyl chain attached through an ether linkage at the O2-position.
DiacylglycerophosphatesCHEMONTID:0001504Glycerophosphates in which the glycerol is esterified ta two positions with to fatty acids.
Acyclic acetylenesCHEMONTID:0002847Acyclic hydrocarbons containing one or more acetylene groups.
Pyrimidinecarboxylic acids and derivativesCHEMONTID:0001319Compounds containing a pyrimidine ring which bears a carboxylic acid group (or a derivative thereof).
MonoacylglycerophosphatesCHEMONTID:0001683Monacylglyerophosphates in which the glycerol moiety is esterified at only position, and is attached to a phosphate group.
PyridinecarboxamidesCHEMONTID:0001326Compounds containing a pyridine ring bearing a carboxamide.
TriazolidinonesCHEMONTID:0001327Compounds containing a triazolidine ring which bears a ketone group.
Lysophosphatidylinositol monophosphatesCHEMONTID:0001330Glycerophosphoinositol monophosphates where the glycerol is esterified with one fatty acid.
PhosphatidylinositolsCHEMONTID:0001344Glycerophosphoinositols where the glycerol is esterified with two fatty acids.
Benzoic acid estersCHEMONTID:0001350Ester derivatives of benzoic acid.
Acyclic triterpenoidsCHEMONTID:0001351Triterpenoids that do not contain a cycle.
LysophosphatidylinositolsCHEMONTID:0001355Glycerophosphoinositols (molecules containing an inositol moiety attached to the phosphate group linked to a glycerol) where the glycerol is esterified with one fatty acid.
MonosaccharidesCHEMONTID:0001540Compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn.
Acyclic diterpenoidsCHEMONTID:0001357Diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle.
PhosphatidylglycerolsCHEMONTID:0001358Glycerophosphoglycerols in which two fatty acids are bonded to the 1-glycerol moiety through ester linkages.
Flavonoid O-glycosidesCHEMONTID:0001583Compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
FlavanonesCHEMONTID:0001632Compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a ketone at the carbon C3.
PhosphatidylserinesCHEMONTID:0001367Glycerophosphoserines in which two fatty acids are bonded to the glycerol moiety through ester linkages.
PyridoindolonesCHEMONTID:0001374Pyridoindoles with a structure that contains an indole moiety bearing a ketone. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
LysophosphatidylserinesCHEMONTID:0001377Glycerophosphoserines (molecules containing a serine moiety attached to the phosphate group linked to a glycerol) with one fatty acid bonded to the glycerol moiety through an ester linkage.
Chlorinated dibenzofuransCHEMONTID:0001378Organic compounds containing a chlorine atom attached to a dibenzofuran moiety.
GlucuronosphingolipidsCHEMONTID:0001388Sphingolipids in which the sphingosine base is linked to a glucuronic acid moiety.
PhosphatidylethanolaminesCHEMONTID:0001393Glycerophosphoetahnolamines in which two fatty acids are bonded to the glycerol moiety through ester linkages.
PhosphoceramidesCHEMONTID:0001427Compounds containing an n-acyl-ceramide phosphate skeleton.
1-alkyl,2-acyl-glycerol-3-phosphoserinesCHEMONTID:0001395Glycerophosphoserines that contain exactly two fatty acyl chains attached to the glycerol moiety, one through an ester and the other through an ether linkage.
1-(1Z-alkenyl),2-acyl-glycerophosphatesCHEMONTID:0001397Glycerophosphates that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
Menthane monoterpenoidsCHEMONTID:0001401Monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
ImidazolinonesCHEMONTID:0001402Organic compounds containing an imidazolinone moiety, which is an imidazoline ring bearing a ketone.
Ergosterols and derivativesCHEMONTID:0001403Steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.
1-alkyl,2-acylglycerophosphatesCHEMONTID:0001404Glycerophosphates in which the O-1 atom of the glycerol is bonded to a fatty acid (saturated or unsaturated) through an ether linkage, and the O-2 atom is bonded to another fatty acid through an ester linkage.
LysophosphatidylethanolaminesCHEMONTID:0001405Glycerophosphoetahnolamines (molecules containing an ethanolamine moiety attached to the phosphate group linked to a glycerol) with one fatty acid chain bonded to the glycerol moiety through an ester linkage.
MonoalkylglycerophosphatesCHEMONTID:0001406Compounds containing glycerophosphate moiety attached to an fatty acyl chain through an ether bond.
1-(1Z-alkenyl),2-acylglycerophosphoserinesCHEMONTID:0001407Glycerophosphoserines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
PhosphatidylcholinesCHEMONTID:0001408Glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
1-acyl,2-alkylglycerophosphoethanolaminesCHEMONTID:0001409Glycerophosphoethanolamines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O1-position, and one alkyl chain attached through an ether linkage at the O2-position.
LysophosphatidylcholinesCHEMONTID:0001413Glycerophosphocholines (molecules containing a choline moiety attached to the phosphate group linked to a glycerol) in which the glycerol is esterified with one fatty acid each through an ester linkage.
MonoalkylglycerophosphocholinesCHEMONTID:0001414Compounds containing glycerophosphocholine moiety attached to an fatty acyl chain through an ether bond.
1-phosphoribosyl-imidazolecarboxamidesCHEMONTID:0001417Organic compounds containing the imidazolecarboxamide linked to a ribose phosphate through a 1-2 bond.
Glycidol estersCHEMONTID:0001421Compounds containing an ester derivative of glycidol (2,3-Epoxy-1-propanol).
Other hydroxyeicosapolyenoic acidsCHEMONTID:0001422Hydroxyeicosapolyenoic acids which do not belong to the Hydroxyeicosapentaenoic acids, the Hydroxyeicosatetraenoic acids, or the Hydroxyeicosatrienoic acids.
Thia fatty acidsCHEMONTID:0001423Fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain.
Sulfated fatty acidsCHEMONTID:0001425Fatty acids containing linked to a sulfate group linked to its tail.
Pyrophosphatidic acidsCHEMONTID:0001426Lipids structurally characterized by the presence of a glycerol moiety bonded to two aliphatic chains through ester linkages, and to a pyrophosphate group.
GangliosidesCHEMONTID:0001439Lipid molecules composed of a glycosphingolipid (ceramide and saccharide) with one or more sialic acids linked on the sugar chain. They are usually oligoglycosylceramides derived from lactosylceramide and containing a sialic acid residue such as N-acetylneuraminic acid.
SulfatidesCHEMONTID:0001440An hydrogen sulfate esters of glycosphingolipids.
Steroid glucuronide conjugatesCHEMONTID:0001447Sterol lipids containing a glucuronide moiety linked to the steroid skeleton.
Furoic acidsCHEMONTID:0001448Organic compounds containing a furoic acid moiety, with a structure characterized by a furan ring bearing a carboxylic acid group at the C2 or C3 carbon atom.
CephamsCHEMONTID:0001456Organic compounds containing the 5-thia-1-azabicyclo[4.2.0]octan-8-one nucleus.
PenemsCHEMONTID:0001457Organic heterocyclic compounds containing a penem moiety, which is a 2,3-didehydropenam derivative.
PyrethroidsCHEMONTID:0001461Organic compounds similar to the pyrethrins. Some pyrethroids containing a chrysanthemic acid esterified with a cyclopentenone (pyrethrins), or with a phenoxybenzyl group.
Mannosylerythritol lipidsCHEMONTID:0001462Lipids containing a mannosylerylthritol skeleton, which is 1-O-b-mannopyranosyl-meso-erythritol.
3-(3-hydroxyalkanoyloxy)alkanoic acidsCHEMONTID:0001463Organic compounds containing a 3-hydroxyalkanoic acid linked to another 3-hydroxyalkanoic acid through the hydroxyl group at the 3-position.
Androgens and derivativesCHEMONTID:00014673-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.
Gluco/mineralocorticoids, progestogins and derivativesCHEMONTID:0001468Steroids with a structure based on a hydroxylated prostane moiety.
Cholesterols and derivativesCHEMONTID:0001469Compounds containing a 3-hydroxylated cholestane core.
Miscellaneous aluminatesCHEMONTID:0001471Inorganic compounds in which the largest metallic oxoanion is aluminate, to which either no atom or a non metal atom is bonded.
Miscellaneous antimonatesCHEMONTID:0001472Inorganic compounds in which the largest metallic oxoanion is antimonate, to which either no atom or a non metal atom is bonded.
Miscellaneous antimonitesCHEMONTID:0001473Inorganic compounds in which the largest metallic oxoanion is antimonite, to which either no atom or a non metal atom is bonded.
Miscellaneous arsenatesCHEMONTID:0001474Inorganic compounds in which the largest metallic oxoanion is arsenate, to which either no atom or a non metal atom is bonded.
Miscellaneous arsenitesCHEMONTID:0001475Inorganic compounds in which the largest metallic oxoanion is arsenite, to which either no atom or a non metal atom is bonded.
Miscellaneous boratesCHEMONTID:0001476Inorganic compounds in which the largest metallic oxoanion is borate, to which either no atom or a non metal atom is bonded.
Miscellaneous ferratesCHEMONTID:0001477Inorganic compounds in which the largest metallic oxoanion is ferrate, to which either no atom or a non metal atom is bonded.
Miscellaneous manganatesCHEMONTID:0001478Inorganic compounds in which the largest metallic oxoanion is manganate, to which either no atom or a non metal atom is bonded.
Miscellaneous molybdatesCHEMONTID:0001479Inorganic compounds in which the largest metallic oxoanion is molybdate, to which either no atom or a non metal atom is bonded.
Miscellaneous plumbatesCHEMONTID:0001480Inorganic compounds in which the largest metallic oxoanion is plumbate, to which either no atom or a non metal atom is bonded.
Miscellaneous plumbitesCHEMONTID:0001481Inorganic compounds in which the largest metallic oxoanion is plumbite, to which either no atom or a non metal atom is bonded.
Miscellaneous silicatesCHEMONTID:0001482Inorganic compounds in which the largest metallic oxoanion is silicate, to which either no atom or a non metal atom is bonded.
Miscellaneous stannatesCHEMONTID:0001483Inorganic compounds in which the largest metallic oxoanion is stannate, to which either no atom or a non metal atom is bonded.
Miscellaneous stannitesCHEMONTID:0001484Inorganic compounds in which the largest metallic oxoanion is stannite, to which either no atom or a non metal atom is bonded.
Miscellaneous telluratesCHEMONTID:0001485Inorganic compounds in which the largest metallic oxoanion is tellurate, to which either no atom or a non metal atom is bonded.
Miscellaneous telluritesCHEMONTID:0001486Inorganic compounds in which the largest metallic oxoanion is tellurite, to which either no atom or a non metal atom is bonded.
Miscellaneous tetrahydroxyboratesCHEMONTID:0001487Inorganic compounds in which the largest metallic oxoanion istetrahydroxyborate, to which either no atom or a non metal atom is bonded.
Miscellaneous tungstatesCHEMONTID:0001488Inorganic compounds in which the largest metallic oxoanion is tungstate, to which either no atom or a non metal atom is bonded.
Miscellaneous orthovanadatesCHEMONTID:0001489Inorganic compounds in which the largest metallic oxoanion is orthovanadate, to which either no atom or a non metal atom is bonded.
Cholesteryl estersCHEMONTID:0001490Compounds containing an esterified cholestane moiety.
2',3'-cyclic purine nucleotidesCHEMONTID:0001494Purine nucleotides in which the oxygen atoms linked to the C2 and C3 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.
2',3'-cyclic pyrimidine nucleotidesCHEMONTID:0001495Pyrimidine nucleotides in which the oxygen atoms linked to the C2 and C3 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.
3',5'-cyclic purine nucleotidesCHEMONTID:0001502Purine nucleotides in which the oxygen atoms linked to the C3 and C5 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.
3',5'-cyclic pyrimidine nucleotidesCHEMONTID:0001503Pyrimidine nucleotides in which the oxygen atoms linked to the C3 and C5 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.
Other hydroperoxyeicosapolyenoic acidsCHEMONTID:0001525Hydroperoxyeicosapolyenoic acids which do not belong to the hydroperoxyeicosapentaenoic acids, the hydroperoxyeicosatetraenoic acids, or the hydroperoxyeicosatrienoic acids.
Heterocyclic fatty acidsCHEMONTID:0001989Fatty acids containing a heterocyclic attached to the acyl chain.
Diterpene lactonesCHEMONTID:0001538Diterpenoids containing a lactone moiety.
DisaccharidesCHEMONTID:0001542Compounds containing two carbohydrate moieties linked to each to each other through a glycosidic bond, no set of three or more glycosidically linked carbohydrate units.
Vitamin K compoundsCHEMONTID:0001547Quinone lipids containing a methylated naphthoquinone ring structure, and vary in the aliphatic side chain attached at the 3-position.
Cardenolides and derivativesCHEMONTID:0001555Steroid lactones containing a furan-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative.
Bufanolides and derivativesCHEMONTID:0001557Steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative.
Withanolides and derivativesCHEMONTID:0001560C28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring.
Monocyclic monoterpenoidsCHEMONTID:0001563Monoterpenoids containing 1 ring in the isoprene chain.
Bicyclic monoterpenoidsCHEMONTID:0001564Monoterpenoids containing exactly 2 rings, which are fused to each other.
Iridoids and derivativesCHEMONTID:0001565Monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.
Retinoid estersCHEMONTID:0001575Ester derivatives of retinoic acid. These are obtained by formal condensation of the hydroxy group of retinol with the carboxy group of any carboxylic acid.
Allylic alcoholsCHEMONTID:0001576Organic compounds containing an alcohol group attached to the allyl functional group CH2=CHCH2.
Triterpene glycosidesCHEMONTID:0001580Triterpenoids in which an isoprene unit is glycosylated.
PiperidinedionesCHEMONTID:0001582Compounds containing a piperidine ring which bears two ketones.
Flavan-3-olsCHEMONTID:0003012Flavans that bear and hydroxyl group at position 3 (B ring), but not at position 4.
OrganosulfonamidesCHEMONTID:0001585Compounds containing the sulfonamide functional group, an amide of sulfonic acid with the general structure R1S(=O)2N(R2)R3 (R1=alkyl, aryl; R2,R3=H, alkyl, aryl).
Spatane and 4,10-secospatane diterpenoidsCHEMONTID:0001595Diterpenoids with a structure based on the spatane or 4,10-secospatane skeleton. The spatane skeleton is formally derived from a prenylgermacrane by 1,5- and 6,10-cyclisation.
Acyclic sesterterpenoidsCHEMONTID:0001596Sesterterpenoids (compounds made of five consecutive isoprene units) that do not contain a cycle.
HydroxyanthraquinonesCHEMONTID:0001598Compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.
Anthraquinone glycosidesCHEMONTID:0001600Organic compounds containing an anthraquinone moiety glycosidically bound to a carbohydrate moiety.
Carbonyl hydratesCHEMONTID:0001605Organic compounds containing two hydroxyl groups attached to a carbon atom.
PterocarpansCHEMONTID:0001608Benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids.
CarnitinesCHEMONTID:0001609Organic compounds containing the quaternary ammonium compound carnitine.
9,9'-epoxylignansCHEMONTID:0003424Lignans with a structure based on the 9,9'-epoxylignan skeleton, which consists of a tetrahydrofuran that carries two benzyl groups at the 3- and 4-positions. Additionally they are oxygenated at the 2-position to form dibenzylbutyrolactones (oxo group) or a dibenzylbutyrolactols (hydroxyl group).
Purine ribonucleoside monophosphatesCHEMONTID:0001617Nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.
Purine ribonucleoside diphosphatesCHEMONTID:0001618Purine ribobucleotides with diphosphate group linked to the ribose moiety.
Purine ribonucleoside triphosphatesCHEMONTID:0001619Purine ribobucleotides with a triphosphate group linked to the ribose moiety.
Pyrimidine ribonucleoside monophosphatesCHEMONTID:0001620Pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety.
Pyrimidine ribonucleoside diphosphatesCHEMONTID:0001621Pyrimidine ribonucleotides with diphosphate group linked to the ribose moiety.
Pyrimidine ribonucleoside triphosphatesCHEMONTID:0001622Pyrimidine ribobucleotides with triphosphate group linked to the ribose moiety.
Purine ribonucleoside polyphosphatesCHEMONTID:0001627Purine ribobucleotides with polyphosphate (with 4 or more phosphate) group linked to the ribose moiety.
Pyrimidine ribonucleoside polyphosphatesCHEMONTID:0001628Pyrimidine ribobucleotides with polyphosphate (with 4 or more phosphate) group linked to the ribose moiety.
SerotoninsCHEMONTID:0001637Compounds containing a serotonin moiety, which consists of an indole that bears an aminoethyl a position 2 and a hydroxyl group at position 5.
Naphthopyranone glycosidesCHEMONTID:0001646Compounds containing a carbohydrate moiety glycosidically linked to a naphthopyranone moiety.
Tyrosol estersCHEMONTID:0001648Tyrosol derivatives in the hydroxyl group of the hydroxyethyl moiety is replaced an o-ester group.
Biopterins and derivativesCHEMONTID:0001651Coenzymes containing a 2-amino-pteridine-4-one derivative. They are mainly synthesized in several parts of the body, including the pineal gland.
Benzyl estersCHEMONTID:0001654Aromatic compounds containing an esterified benzyl group.
AcetalsCHEMONTID:0001656Compounds having the structure R2C(OR')2 ( R' not Hydrogen) and thus diethers of geminal diols. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H ). Mixed acetals have different R' groups.
Carboxylic acid imidesCHEMONTID:0001657Carboxylic acid derivatives containing two carbonyl groups where the carbon atoms are both linked to the same nitrogen atom.
Secondary alcoholsCHEMONTID:0001661Compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).
Long-chain ceramidesCHEMONTID:0001669Ceramides bearing a long chain fatty acid.
Tertiary alcoholsCHEMONTID:0001670Compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).
KetiminesCHEMONTID:0001673Organic compounds bearing the ketimine functional group, with the general structure R2C=NR' ( R is not a hydrogen ).
Steroidal saponinsCHEMONTID:0002364Saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.
AminopyrazinesCHEMONTID:0001694Organic compounds containing an amino group attached to a pyrazine ring.
Solanidines and derivativesCHEMONTID:0001703Steroids with a structure based on the solanidane skeleton. Solanidane arises from the conversion of a cholestane side-chain into a bicyclic system.
Spirosolanes and derivativesCHEMONTID:0001704Steroidal alkaloids with a structure containing a spirosolane skeleton. Siporosolane is a polycyclic compound that is characterized by a 1-oxa-6-azaspiro[4.5]decane moiety where the oxolane ring is fused to a docosahydronaphth[2,1:4',5']indene ring system. Spirosolane arises from the conversion of a cholestane side-chain into a bicyclic system containing a piperidine and a tetrahydrofuran ring.
GingerolsCHEMONTID:0001705Compounds containing a gingerol moiety, which is structurally characterized by a 4-hydroxy-3-methoxyphenyl group substituted at the C6 carbon atom by a 5-hydroxy-alkane-3-one.
GingerdiolsCHEMONTID:0001706Compounds containing a gingerdiol moiety, which is structurally characterized by a 4-hydroxy-3-methoxyphenyl group substituted at the C6 carbon atom by an alkane-2,4-diol.
GingerdionesCHEMONTID:0001707Compounds containing a gingerdione moiety, which is structurally characterized by a 4-hydroxy-3-methoxyphenyl group substituted at the C6 carbon atom by an alkane-2,4-dione.
ShogaolsCHEMONTID:0001708Ginger derivatives containing a shogaol moiety, which consists of a benzene ring bearing a dec-4-en-3-one moiety, a methoxyphenyl group, a hydroxyl group and at positions 1, 3, and 4, respectively.
ParadolsCHEMONTID:0001709Compounds containing a paradol moiety, which is consists of a benzene ring with a decan-3-one moiety, a methoxyl group, and a hydroxyl group at positions 1,3, and 4 respectively.
HydroxyquinolonesCHEMONTID:0001714Compounds containing a quinoline moiety bearing a hydroxyl group and a ketone. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.
HydroquinolonesCHEMONTID:0001716Compounds containing a hydrogenated quinoline bearing a ketone group.
Other glycerophosphoinositol phosphatesCHEMONTID:0001718Glycerophosphoinositol phosphates not belonging to Lysophosphatidylinositol Phosphates, or the Phosphatidylinositol Phosphates.
DiacylglycerophosphodiradylglycerolsCHEMONTID:0001719Glycerophosphodiradylglycerols that carry exactly two acyl chains attached to the glycerol moiety through ester linkages.
LysophosphatidylglycerophosphatesCHEMONTID:0001720Glycerophosphates (molecules containing a phosphate group linked to a glycerol) where the glycerol is esterified with one fatty acid.
Wax estersCHEMONTID:0001723Mixtures of long-chain apolar lipids. They are usually esters of an alcohol other than glycerol and a long chain acid.
Chloropropanol estersCHEMONTID:0001725Compounds containing an ester derivative of chloropropanol.
DiacylglycosylglycerophospholipidsCHEMONTID:0001727Glycosylglycerophospholipids, where the glycerol moiety is esterified with two fatty acyl chains.
DioxopiperazinesCHEMONTID:0001731Compounds containing a piperazine ring bearing two ketone groups. These include the alkaloid class of naturally occurring 2,5-dioxopiperazines.
Flavonoid C-glycosidesCHEMONTID:0001737Compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
CyanolipidsCHEMONTID:0001744Lipids containing a five-carbon backbone that comprises a nitrile moiety together with a methylene group or double bond, and one or two hydroxyl groups. Cyanolipids are divided in four categories (type I-IV).
8,2'-cyclic purine nucleotidesCHEMONTID:0001752Purine nucleotides in which the atom linked to the C2 carbon atom of the ribose moiety is bonded the C8 carbon atom of the purine moiety.
Alkyl glycosidesCHEMONTID:0002125Lipids containing a glycosyl moiety (one or several units) linked to the hydroxyl group of a fatty alcohol.
Diterpene glycosidesCHEMONTID:0001755Diterpenoids in which an isoprene unit is glycosylated.
Colensane and clerodane diterpenoidsCHEMONTID:0001757Diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.
FuranoflavonesCHEMONTID:0001759Polycyclic aromatic compounds containing a furan ring fused to a flavan-3-one.
Dolabellane and neodolabellane diterpenoidsCHEMONTID:0001760Diterpenoids with a structure based on the dolabellane skeleton (3a,6,10-trimethyl-1-(propan-2-yl)-cyclopenta[11]annulene) or the neodolabellane skeleton.
RhamnolipidsCHEMONTID:0001765Glycolipids structurally characterized by a glycosyl head group, in this case a rhamnose moiety, and a 3-(hydroxyalkanoyloxy)alkanoic acid (HAA) fatty acid tail.
GibberellinsCHEMONTID:0001767Diterpenoids containing the gibberellane skeleton ((8S)-4,4,8-trimethyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane), an aliphatic four-ring system.
PyrroloindolizinesCHEMONTID:0001769Compounds containing a pyrroloindolizine moiety, which consists of a pyrrole ring fused to an indolizine.
GlycosylmonoradylglycerolsCHEMONTID:0003819Glycosylglycerols that carry exactly one acyl chain attached to the glycerol moiety.
Brassinolides and derivativesCHEMONTID:0001774Cholestane based steroid lactones containing benzo[c]indeno[5,4-e]oxepin-3-one.
Illudanes and illudinsCHEMONTID:0001777Sesquiterpenoids containing either the illudane moiety (based on a 3,6,6,7b-tetramethyl-decahydro-1H-cyclobuta[e]indene ring system), the illudin moiety (2',2',4',6'-tetramethyl-octahydrospiro[cyclopropane-1,5'-indene]), or a derivative thereof.
Aromadendrane sesquiterpenoidsCHEMONTID:0001781Sesquiterpenoids with a structure based on an aromadendrane (a cyclopropa[e]azulene derivative) skeleton. Some aromadendrane sesquiterpenoids are found in essential oils. Certain aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis were found to possess antifungal activities.
TrichothecenesCHEMONTID:0001789Sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.
Spironolactones and derivativesCHEMONTID:0001807Steroid lactones with a structure based on the spironolactone skeleton.
PeptidomimeticsCHEMONTID:0001813Compounds containing non-peptidic structural elements that is capable of mimicking or antagonizing the biological action(s) of a natural parent peptide.
IsoindolonesCHEMONTID:0001820Aromatic polycyclic compounds that an isoindole bearing a ketone.
Hopane triterpenoidsCHEMONTID:0001824Triterpenoids with a structure based on the hopane skeleton.
BacteriohopanoidsCHEMONTID:0001826Bacterial terpenoids structurally characterized by a C30 skeleton, which is usually conjugated to a C5 (usually hydroxylated) unit linked by a carbon-carbon bond.
IsoflavanonesCHEMONTID:0001827Polycyclic compounds containing an isoflavan skeleton which bears a ketone at position C4.
IsoflavanolsCHEMONTID:0001828Polycyclic compounds containing a hydroxylated isoflavan skeleton.
M-terphenylsCHEMONTID:0001829Terphenyls with a structure containing the 1,3-diphenylbenzene skeleton.
O-terphenylsCHEMONTID:0001836Terphenyls with a structure containing the 1,2-diphenylbenzene skeleton.
Phenyltetrazolines and derivativesCHEMONTID:0001843Compounds containing a phenyltetrazoline skeleton, which consists of a tetrazoline bound to a phenyl group.
Bromodiphenyl ethersCHEMONTID:0001845Compounds that contain two benzene groups linked to each other via an ether bond, and where at least one ring is substituted with a bromo group.
AcetanilidesCHEMONTID:0001846Organic compounds containing an acetamide group conjugated to a phenyl group.
1Z-alkenylglycerophosphocholinesCHEMONTID:0003823Glycerophosphocholines that carry exactly one 1Z-alkenyl chain attached to the glycerol moiety through an ether linkage.
CarbonucleotoidsCHEMONTID:0001848Organic peptide derivatives with monosaccharide units linked through Phosphate diester bonds.
CarbopeptoidsCHEMONTID:0001849Oligosaccharides having carbohydrate subunits linked to one another by amide bonds.
PyridazinoindazolesCHEMONTID:0001856Compounds containing a pyridazinoindazole moiety, which consists of a pyridazine ring fused to an indazole.
Naphthyridine carboxylic acids and derivativesCHEMONTID:0001858Compounds containing a naphthyridine moiety, where one of the ring atoms bears a carboxylic acid group.
PyrrolocarbazolesCHEMONTID:0001865Compounds containing a pyrrolocarbazole moiety, which is a tetracyclic heterocycle which consists of a pyrrole ring fused to a carbazole.
PhthalidesCHEMONTID:0001873Compounds containing a 3-hydrocarbylidene-2-benzofuran-1(3H)-one moiety,.
BiphenylcarbonitrilesCHEMONTID:0001892Organic compounds containing an acetonitrile with one hydrogen replaced by a biphenyl group.
HalopyrimidinesCHEMONTID:0001893Aromatic compounds containing a halogen atom linked to a pyrimidine ring. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
ThienoquinolinesCHEMONTID:0001896Heterocyclic compounds containing a thiophene ring fused to a quinoline. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.
Pyrimidine ribonucleoside bisphosphatesCHEMONTID:0001904Pyrimidine ribobucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety.
Alpha carbolinesCHEMONTID:0001913Organic compounds containing a pyrido[2,3-b]indole core (which is a pyridine fused to an indole).
Beta carbolinesCHEMONTID:0001914Compounds containing a 9H-pyrido[3,4-b]indole moiety.
Delta carbolinesCHEMONTID:0001915Aromatic compounds containing a delta carboline moiety, which consists of a pyridine fused to and indole to form pyrido[3,2-b]indole.
Gamma carbolinesCHEMONTID:0001916Polycyclic aromatic compounds containing a gamma-carbazole(5H-pyrido[4,3-b]indole) moiety, with a structure characterized by the presence of pyridine fused to the pyrrole ring of an indole.
PyrimidinethionesCHEMONTID:0001921Compounds containing a pyrimidine ring that bears a thioketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
ThiazolidinethionesCHEMONTID:0001923Heterocyclic compounds containing a thiazolidinethione ring which bears one thioketone group.
AminopyridazinesCHEMONTID:0001924Organic compounds containing an amino group attached to a pyridazine ring.
AminobenzenesulfonamidesCHEMONTID:0001925Organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.
NitropyrimidinesCHEMONTID:0001927Compounds containing a pyrimidine ring which bears a nitro group. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
TetrahydropyridinesCHEMONTID:0001934Derivatives of pyridine in which two double bonds in the pyridine moiety are reduced by adding four hydrogen atoms.
Prenylated hydroquinonesCHEMONTID:0002801Quinones with a structure characterized by the hydroquinone ring substituted by an prenyl side-chain.
SphingosylphosphorylcholinesCHEMONTID:0001972Sphingolipids containing a sphingosine attached to the phosphate group of a phosphocholine.
PyridinylpiperazinesCHEMONTID:0001976Compounds containing a pyridinylpiperazine skeleton, which consists of a pyridine linked (not fused) to a piperazine by a bond by a single bond that is not part of a ring.
PyrimidinylpiperazinesCHEMONTID:0001977Compounds containing a pyrimidinylpiperazine skeleton, which consists of a pyrimidine linked (not fused) to a piperazine by a bond. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. Piperazine is a six-membered heterocyclic compound consisting of two nitrogen atoms and four carbon atoms.
Bipyrimidines and oligopyrimidinesCHEMONTID:0001978Organic compounds containing two or more pyrimidine rings directly linked to each other. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
PhenylpiperazinesCHEMONTID:0001984Compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group.
Nitrobenzoic acids and derivativesCHEMONTID:0001992Compounds containing a nitrobenzoic acid moiety, which consists of a benzene ring bearing both a carboxylic acid group and a nitro group on two different ring carbon atoms.
2',5'-cyclic purine nucleotidesCHEMONTID:0001993Purine nucleotides in which the oxygen atoms linked to the C2 and C5 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.
PurinethionesCHEMONTID:0001998Purines in which the purine moiety bears a thioketone.
DithioxanthinesCHEMONTID:0001999Compounds containing a dithioxanthine moiety, a xanthine derivative obtained by replacing the two ketone groups by two thioketone groups.
Mutilane diterpenoidsCHEMONTID:0002930Diterpenoids with a structure based on the mutilane skeleton.
Triquinane sesquiterpenoidsCHEMONTID:0002004Sesquiterpenoids with a structure based on the triquinane backbone.
Thiazolecarboxylic acids and derivativesCHEMONTID:0002007Heterocyclic compounds containing a thiazole ring which bears a carboxylic acid group (or a derivative thereof).
Indolecarboxamides and derivativesCHEMONTID:0002014Compounds containing a carboxamide group attached to an indole.
Thiophene carboxamidesCHEMONTID:0002018Compounds containing a thiophene ring which bears a carboxamide.
PhenylpyrazolesCHEMONTID:0002019Compounds containing a phenylpyrazole skeleton, which consists of a pyrazole bound to a phenyl group.
UreidesCHEMONTID:0002022Compounds containing an ureide group with the general structure R1-CO-NH-CO-N(R)2R3, formally derived by the acylation of urea.
Thioketone s-oxidesCHEMONTID:0002025Organic compounds containing a functional group with the general structure R2C=S=O (R not H).
DipyrrinsCHEMONTID:0002028Compounds containing two pyrrole rings fused via a methine (-C=) group.
SemioxamazonesCHEMONTID:0002029Compounds containing a semioxamazone functional group, with the structure R2C=NNHC(=O)C(=O)NH2, which is derived from the condensation of aldehydes or ketones with semioxamazide.
IsoselenocyanatesCHEMONTID:0002032Organic compounds containing the isoselenocyanate group, an isocyanate analogue with the general formula RN=C=Se.
Carbonyl imidesCHEMONTID:0002033Organic compounds containing a carbonyl imide group (a carbon atom linked through a double bond to an oxygen atom, which is in turn linked to a nitrogen atom).
Carbonyl oxidesCHEMONTID:0002034Organic compounds containing a carbonyl imide group (a carbon atom linked through a double bond to an oxygen atom, which is in turn linked to an oxygen atom).
FormazansCHEMONTID:0002038Compounds containing the formazan group with the formula R1(R2)NN=CHN=NR3 (R1,R2,R3=H, alkyl, or aryl).
SelenolsCHEMONTID:0002040Organic compounds that contains the functional group with the connectivity R-Se-H.
SelonesCHEMONTID:0002041Organic compounds that contains the functional group with the connectivity RC(=Se)R' (R,R' not H).
AgarofuransCHEMONTID:0002051Organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]dodec-2-ene).
Silyl enol ethersCHEMONTID:0002053Organic compounds containing an enolate bonded through its oxygen terminus to an organosilicon group.
FurazansCHEMONTID:0002056Compounds containing a furazan moiety, which consists of a five-membered aromatic ring with 1 oxygen and 2 nitrogen atoms at positions 2, 1, and 5, respectively.
Sulfite estersCHEMONTID:0002074Organic compounds containing an organic group attached to the sulfite oxoanion, with the formula R[SO3]2-.
IsoxazolidinonesCHEMONTID:0002084Organic heterocyclic compounds containing an isoxazolidine moiety, which consists of an isoxazolidine ring which bears a ketone.
Pyrazine carboxylic acids and derivativesCHEMONTID:0002265Heterocyclic compounds containing a pyrazine ring substituted by one or more carboxylic acid groups (or derivatives thereof).
AcyloinsCHEMONTID:0002088Organic compounds containing an alpha hydroxy ketone. Acyloins are formally derived from reductive coupling of carboxylic acyl groups.
OxoprolinesCHEMONTID:0002089Compounds containing an oxoproline moiety, which consists of a pyrrolidine ring bearing a carboxylic acid group at the ring position 2, and a ketone group.
Alkanesulfonic acids and derivativesCHEMONTID:0003136Organic acids containing an alkane chain linked to a sulfonic acid group. They have the general structure RS(=O)2-OR' (R = alkyl, R' = any atom).
Phenarsazines and derivativesCHEMONTID:0002104Polycyclic aromatic compounds containing two benzene rings joined by a 1,4-azarsine (or a derivative thereof).
Glycosyl compoundsCHEMONTID:0002105Carbohydrate derivatives in which a sugar group is bonded through its anomeric carbon to another group via a C-, S-,N-,O-, or Se- glycosidic bond.
BenzodioxinopyrrolesCHEMONTID:0002107Polycyclic aromatic compounds containing a pyrrole ring fused to the dioxin ring of a benzo-p-dioxin.
BenzomorpholinesCHEMONTID:0002108Polycyclic aromatic compounds containing a benzene ring fused to a morpholine ring.
FuroindazolesCHEMONTID:0002110Polycyclic aromatic compounds containing a furan ring fused to the benzene ring of an indazole.
StanninesCHEMONTID:0002115Compounds containing a benzene analogue in which one of the carbon atoms is replaced by a tin atom.
StannolesCHEMONTID:0002116Compounds containing a five-member aromatic ring with one tin atom and four carbon atoms.
QuassinoidsCHEMONTID:0002119A group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.
2',5'-cyclic pyrimidine nucleotidesCHEMONTID:0002121Pyrimidine nucleotides in which the oxygen atoms linked to the C2 and C5 carbon atoms of the ribose moiety are both bonded the same phosphorus atom of the phosphate group.
P-terphenylsCHEMONTID:0002126Terphenyls with a structure containing the 1,4-diphenylbenzene skeleton.
MonothioketalsCHEMONTID:0002130Compounds containing a monothioketal functional group with the general structure R2C(OR')(SR') with (R = any atom but H).
DithioketalsCHEMONTID:0002133Compounds containing a dithioketal functional group with the general structure R2C(SR')2 with R, R' = organyl.
Purine deoxyribonucleoside monophosphatesCHEMONTID:0002135Purine ribonucleotides with one monophosphate group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Purine deoxyribonucleoside diphosphatesCHEMONTID:0002136Purine ribonucleotides with one diphosphate group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Purine deoxyribonucleoside triphosphatesCHEMONTID:0002137Purine ribonucleotides with one triphosphate group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Purine deoxyribonucleoside polyphosphatesCHEMONTID:0002138Purine ribonucleotides with one polyphosphate (with at least four repetitively linked phosphates) group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Pyrimidine deoxyribonucleoside bisphosphatesCHEMONTID:0002149Pyrimidine ribobucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Pyrimidine deoxyribonucleoside diphosphatesCHEMONTID:0002150Pyrimidine ribobucleotides with one diphosphate group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Pyrimidine deoxyribonucleoside monophosphatesCHEMONTID:0002151Pyrimidine ribobucleotides with one monophosphate group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Pyrimidine deoxyribonucleoside polyphosphatesCHEMONTID:0002152Pyrimidine ribobucleotides with one polyphosphate (with at least four repetitively linked phosphates) group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Pyrimidine deoxyribonucleoside triphosphatesCHEMONTID:0002153Pyrimidine ribobucleotides with one triphosphate group attached to one hydroxyl group of the ribose moiety, which lacks a hydroxyl group at one or more positions.
Purine deoxyribonucleoside bisphosphatesCHEMONTID:0002173Purine ribonucleotides with one phosphate group attached to each of two different hydroxyl groups of the ribose moiety, which lacks a hydroxyl group at one or more positions.
PhenyltriazolesCHEMONTID:0002183Organic aromatic compounds containing a phenyl group substituted with a triazole ring.
PiperazinesulfonamidesCHEMONTID:0002184Organic cyclic compounds containing a sulfonamide group attached to a piperazine ring.
Pachysanane triterpenoidsCHEMONTID:0002190Triterpenoids with a structure based on the pachysanane skeleton, a friedelane derivative which has the C-28 methyl group attached to C-16.
ErgopeptamsCHEMONTID:0002193Tripeptidic noncyclol ergot alkaloids. The structure of ergopeptams is similar to ergopeptines except that L-proline is exchanged by D-proline, and the tripeptide chain is a noncyclol lactam.
NaphthylquinolinesCHEMONTID:0002196Polycyclic aromatic compounds containing a naphthene moiety linked to a quinoline through a CC or CN single bond.
SophorolipidsCHEMONTID:0002201Glycolipids containing a sophorose moiety linked glycosidically to the hydroxyl group of a 17-hydroxy-C18 saturated fatty acid. The carboxyl group of the fatty acid can be linked to the 4'-hydroxyl of the second glucose to form a lactone.
HydropyrimidinesCHEMONTID:0002202Compounds containing a hydrogenated pyrimidine ring (i.e. containing less than the maximum number of double bonds.).
Sugar alcoholsCHEMONTID:0002210Hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
ButenolidesCHEMONTID:0002223Dihydrofurans with a carbonyl group at the C2 carbon atom.
Secondary aminesCHEMONTID:0002451Amines having the nitrogen atom linked to exactly two hydrocarbyl groups.
IsoxazolinonesCHEMONTID:0002232Compounds containing an isoxazoline ring that bears a ketone group.
AzinesCHEMONTID:0002392Hydrazine derivatives in which the hydrazine group is conjugated to two aldehydes (forming aldazines) or ketones (forming ketazines).
Arylsulfonic acids and derivativesCHEMONTID:0002237Organic compounds containing an aryl group attached to the sulfonic acid group (or a derivative thereof).
Tertiary aminesCHEMONTID:0002452Amines having the nitrogen atom linked to exactly three hydrocarbyl groups.
ThiopyranoquinolinesCHEMONTID:0002240Polycyclic compounds containing a thiopyran ring fused to a quinoline moiety. Quinoline or benzo[b]pyridine is a bicyclic compound that consists of benzene fused to a pyridine.
8,2'-cyclic pyrimidine nucleotidesCHEMONTID:0002244Pyrimidine nucleotides in which the atom linked to the C2 carbon atom of the ribose moiety is bonded the C8 carbon atom of the pyrimidine moiety.
Abscisic acids and derivativesCHEMONTID:0002245Terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety.
Thioaldehyde s-oxidesCHEMONTID:0002251Compounds having the general structure RC(=S=O)H.
Quinoline-3-carboxamidesCHEMONTID:0002252Quinolines in which the quinoline ring system is substituted by one carboxamide group at the 3-position.
PyrrolidinecarboxamidesCHEMONTID:0002256Pyrrolidines in which the pyrrolidine rings is substituted at one or more positions by a carboxamide group. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
N-substituted pyrrolesCHEMONTID:0002258Heterocyclic compounds containing a pyrrole ring substituted at position 1.
Pyranopterins and derivativesCHEMONTID:0002263Pterin derivatives in which a pyran ring is fused either to the pyrimidine ring or the pyrazine ring of the pterin moiety.
Indole-3-glycerol-3-phosphatesCHEMONTID:0002280Heterocyclic compounds containing an indole moiety substituted at position 3 by a glycerol-3-phosphate.
Pterin carboxylatesCHEMONTID:0002283Heterocyclic aromatic compounds containing a pterin moiety, in which one ring is substituted by one or more carboxylic acid groups. Pterin is a heterocyclic compound composed of a pteridine ring system (made up of a pyrazine fused to a pyrimidine), with a keto group and an amino group at the 2- and 4- positions, respectively.
PolyolsCHEMONTID:0002286Organic compounds containing more than one hydroxyl groups.
Thiomorpholine carboxylic acids and derivativesCHEMONTID:0002289Heterocyclic compounds containing a thiomorpholine ring substituted by one or more carboxylic acid groups (or derivative thereof). Thiomorpholine a six-membered aliphatic ring containing one nitrogen atom and one sulfur atom at positions 1 and 4 respectively, and four carbon atoms.
Morpholine carboxylic acids and derivativesCHEMONTID:0002307Heterocyclic compounds containing a morpholine ring substituted by one or more carboxylic acid groups (or derivative thereof).
PhenylpyrimidinesCHEMONTID:0002308Polycyclic aromatic compounds containing a benzene ring linked to a pyrimidine ring through a CC or CN bond. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
PiperidinecarboxamidesCHEMONTID:0002312Compounds containing a piperidine ring substituted with a carboxamide functional group.
Piperazine carboxylic acids and derivativesCHEMONTID:0002315Heterocyclic compounds containing a piperazine ring substituted by one or more carboxylic acid groups (or derivatives thereof).
CarbacephemsCHEMONTID:0002318A new class of beta-lactam antibiotics similar in structure to the cephalosporins. They differ from cephalosporins, however, in the substitution of a sulfur atom in the dihydrothiazine ring with a methylene group to form a tetrahydropyridine ring.
Triazole carboxylic acids and derivativesCHEMONTID:0002324Heterocyclic compounds containing a triazole ring substituted by at least one carboxylic acid group (or a derivative thereof).
Thiadiazole sulfonamidesCHEMONTID:0002326Heterocyclic compounds containing a thiazole ring substituted by at least one sulfonamide group.
AminothiazolesCHEMONTID:0002329Compounds containing a thiazole ring substituted by one or more amine groups.
PhenylpyrrolesCHEMONTID:0002334Polycyclic aromatic compounds containing a benzene ring linked to a pyrrole ring through a CC or CN bond.
ImidazolethionesCHEMONTID:0002337Aromatic compounds containing an imidazole ring which bears a thioketone group.
ChromenopyridinesCHEMONTID:0002339Aromatic heterocyclic compounds structurally characterized by a pyridine ring fused to a chromene moiety.
DialkylglycerophosphoglycerophosphatesCHEMONTID:0002343Glycerophosphoglycerophosphates that carry two aliphatic chains (alkyl group) attached to the glycerol moiety.
Methoxybenzoic acids and derivativesCHEMONTID:0002344Benzoic acids in which a hydrogen atom of the benzene ring is replaced by a methoxy group.
NaphthalenecarboxamidesCHEMONTID:0002349Compounds containing a naphthalene moiety, which bears a carboxylic acid amide group at one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene rings.
Pyrazole carboxylic acids and derivativesCHEMONTID:0002350Heterocyclic compounds containing a pyrazole ring in which a hydrogen atom is replaced by a carboxylic acid group.
Nitrite estersCHEMONTID:0002376Ester derivatives of nitro compounds.
LimonoidsCHEMONTID:0002380Highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.
AzomethinesCHEMONTID:0002393Compounds having the general structure RN=CR2 (where R is not a hydrogen atom).
Adianane, fernane, filicane, and neohopane triterpenoidsCHEMONTID:0002400Triterpenoids with a structure based either on the adianane, fernane, filicane, or neohopane skeleton. These are obtained by rearrangement of the moretane skeleton.
Indolecarboxylic acidsCHEMONTID:0002406Compounds containing a carboxylic acid group linked to an indole.
Oxirane carboxylic acidsCHEMONTID:0002409Compounds containing an oxirane ring bearing a carboxylic acid group.
Piperidinecarboxylic acidsCHEMONTID:0002411Compounds containing a piperidine ring which bears a carboxylic acid group.
Pyran carboxylic acidsCHEMONTID:0002412Compounds containing a pyran ring which bears a carboxylic acid group.
Pyridinecarboxylic acidsCHEMONTID:0002414Compounds containing a pyridine ring bearing a carboxylic acid group.
Pyrrolidine carboxylic acidsCHEMONTID:0002416Compounds containing a pyrrolidine ring which bears a carboxylic acid. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
Pyrroline carboxylic acidsCHEMONTID:0002417Heterocyclic compounds containing a pyrroline ring substituted by one or more carboxylic acid groups.
Thiophene carboxylic acidsCHEMONTID:0002419Compounds containing a thiophene ring which bears a carboxylic acid group.
Naphthalenecarboxylic acidsCHEMONTID:0002421Compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
Azetidinecarboxylic acidsCHEMONTID:0002422Organic compounds containing a carboxylic acid group attached to an azetidine ring.
Aziridinecarboxylic acidsCHEMONTID:0002423Organic compounds containing a carboxylic acid group attached to an aziridine ring.
Anthracenecarboxylic acidsCHEMONTID:0002424Organic compounds containing a carboxylic acid group attached to an anthracene ring system.
TellurolsCHEMONTID:0002425Analogues of alcohols and phenols where the oxygen is replaced by a tellurium atom.
TellonesCHEMONTID:0002426Organotellurium compounds with the general formula RC(=Te)R' (R,R\" = organyl).
SelenoethersCHEMONTID:0002429Organic compounds containing a selenoether group, with the general formula RseR' ( where R, R' are not H atoms).
SelenoestersCHEMONTID:0002430Analogues of esters where an oxygen atom is replaced by a selenium atom. They generally have the formula RC(=O)SeR' or RC(=Se)OR'.
TelluroethersCHEMONTID:0002431Organic compounds containing a telluroether group, with the general formula RTeR' ( where R, R' are not H atoms).
Alpha,beta-unsaturated carbonyl compoundsCHEMONTID:0003131Carbonyl compounds with the general structure R#CC(=O)R' or R=CC(=O)R', where R=organyl, R'=H, N, O, organyl group or halide group.
ArtemisininsCHEMONTID:0002440Sesquiterpenoids originally isolated from the herb Artemisia annua. Their structure is based on artemisinin, a tetracyclic compound that contains a 1,2-dioxepane fused to an octahydrobenzopyran moiety. The internal peroxide bridge is believed to be a key to the mode of action of artemisinins.
Organic S-nitroso compoundsCHEMONTID:0004779Organic compounds containing a n-nitroso group -SN=O.
Peroxycarboxylic acidsCHEMONTID:0002446Organic acids with the general formula [H]OOC(R)=O (R = H, organyl group).
PiperidinylpiperazinesCHEMONTID:0002447Heteropolycyclic compounds containing a piperidine ring and a piperazine ring linked together by a single bond that is not part of a ring.
Germacrane sesquiterpenoidsCHEMONTID:0002456Sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups.
NitraminesCHEMONTID:0002459Organyl derivatives of nitramide with the general formula RNHO2 (R = organyl group).
HydrazidinesCHEMONTID:0002464Hydrazine derivatives with the general formula RC(NHNH2)2=NNH2.
SelenocyanatesCHEMONTID:0002470Organic compounds with the general formula RSeC#N.
Selenenyl halidesCHEMONTID:0002471Organoselenium compounds with the general formula RSeX (R = organyl, X = halogen atom).
DiselenidesCHEMONTID:0002472Organoselenium compounds with the general structure R-Se-Se-R' (R,R' = H or organic moiety).
SelenoxidesCHEMONTID:0002473Organoselenium compounds with the general formula RSe(=O)R' (R,R'= organyl).
SeleniranesCHEMONTID:0002476Organoselenium compounds containing a three-member ring consisting of two carbon atoms and one selenium atom.
TelluraldehydesCHEMONTID:0002477Organotellurium compounds with the general formula RC(=Te)H (R = organyl).
DitelluridesCHEMONTID:0002478Organotellurium compounds with the general structure R-Te-Te-R' (R,R' = H or organic moiety).
TelluronesCHEMONTID:0002479Organotellurium compounds with the general formula R[Te](R')(=O)=O (R,R' = organyl).
TelluroxidesCHEMONTID:0002482Organotellurium compounds R[Te](R')=O (R,R' = organyl).
DicarboxdiimidesCHEMONTID:0002483Hydrazine derivatives in which each of the two nitrogen atoms is the central atom of a dicarboximide group.
Hydroxycinnamic acidsCHEMONTID:0002503Compounds containing an cinnamic acid where the benzene ring is hydroxylated.
N-piperazineacetamidesCHEMONTID:0002516Heterocyclic compounds containing a piperazine ring, which N-substituted with an acetamide group.
ChamigranesCHEMONTID:0002517Sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae.
Annonaceous acetogeninsCHEMONTID:0002518Waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.
P-toluquinolsCHEMONTID:0002521Toluene with two hydroxyl group attached to the benzene ring in a para-relationship.
Cyclopropanecarboxylic acidsCHEMONTID:0002525Organic compounds containing a carboxyl group attached to a cyclopropane ring.
1-aminocyclopropane-1-carboxylic acids and derivativesCHEMONTID:0002526Organic compounds containing both a carboxyl group (or a derivative thereof) and an amino group at position C1 of a cyclopropane ring.
PhenylimidazolidinesCHEMONTID:0002547Polycyclic compounds containing an imidazoline substituted by a phenyl group.
Tanshinones, isotanshinones, and derivativesCHEMONTID:0002548A group of abietane-type norditerpenoid quinones.
Tanshinlactones and derivativesCHEMONTID:0002549Oxasteroids with a structure containing an C-17 steroid skeleton, with two oxygen atoms replacing carbon atoms, and one C=O group. They all have one nitrogen atom at the 15-position. Some tanshinlactones have the second oxygen atom at the 11-position and a C=O group at the 12-position. Others have the second oxygen atom at the 12-position and a C=O group at the 11-position.
Isocopalane and spongiane diterpenoidsCHEMONTID:0002550Diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton.
Pyrrole carboxylic acidsCHEMONTID:0002555Heterocyclic compounds containing a pyrrole ring bearing a carboxyl group.
Pyrrole carboxamidesCHEMONTID:0002556Heterocyclic compounds containing a pyrrole ring bearing a carboxamide.
N-substituted phenoxazinesCHEMONTID:0002558Phenoxyazines where the nitrogen atom is linked to an atom other than the hydrogen atom.
AminothiadiazolesCHEMONTID:0002562Thiadiazoles with an amino group attached to the thiadiazole ring.
MethoxypyrazinesCHEMONTID:0002563Pyrazines containing a methoxyl group attached to the pyrazine ring.
Benzoic acidsCHEMONTID:0002565Organic Compounds containing a benzene ring which bears at least one carboxyl group.
PhenyloxazolidinesCHEMONTID:0002574Heterocyclic compounds containing an oxazolidine ring conjugated by a phenyl group.
PhenylisoxazolidinesCHEMONTID:0002575Heterocyclic compounds containing an isoxazolidine conjugated by a phenyl group.
PhenylthiomorpholinesCHEMONTID:0002577Compounds containing a thiomorpholine ring conjugated to a phenyl group. Thiomorpholine a six-membered aliphatic ring containing one nitrogen atom and one sulfur atom at positions 1 and 4 respectively, and four carbon atoms.
2-O-methylated flavonoidsCHEMONTID:0002587Flavonoids with methoxy groups attached to the C2 atom of the flavonoid backbone.
3-O-methylated flavonoidsCHEMONTID:0002588Flavonoids with methoxy groups attached to the C3 atom of the flavonoid backbone.
4-O-methylated flavonoidsCHEMONTID:0002589Flavonoids with methoxy groups attached to the C4 atom of the flavonoid backbone.
5-O-methylated flavonoidsCHEMONTID:0002590Flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.
6-O-methylated flavonoidsCHEMONTID:0002591Flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone.
7-O-methylated flavonoidsCHEMONTID:0002592Flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.
8-O-methylated flavonoidsCHEMONTID:0002593Flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.
2'-O-methylated flavonoidsCHEMONTID:0002594Flavonoids with methoxy groups attached to the C2' atom of the flavonoid backbone.
3'-O-methylated flavonoidsCHEMONTID:0002595Flavonoids with methoxy groups attached to the C3' atom of the flavonoid backbone.
4'-O-methylated flavonoidsCHEMONTID:0002596Flavonoids with methoxy groups attached to the C4' atom of the flavonoid backbone.
2-O-methylated isoflavonoidsCHEMONTID:0002597Isoflavonoids with methoxy groups attached to the C2 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
3-O-methylated isoflavonoidsCHEMONTID:0002598Isoflavonoids with methoxy groups attached to the C3 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
4-O-methylated isoflavonoidsCHEMONTID:0002599Isoflavonoids with methoxy groups attached to the C4 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
5-O-methylated isoflavonoidsCHEMONTID:0002600Isoflavonoids with methoxy groups attached to the C5 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
6-O-methylated isoflavonoidsCHEMONTID:0002601Isoflavonoids with methoxy groups attached to the C6 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
7-O-methylated isoflavonoidsCHEMONTID:0002602Isoflavonoids with methoxy groups attached to the C7 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
8-O-methylated isoflavonoidsCHEMONTID:0002603Isoflavonoids with methoxy groups attached to the C8 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
2'-O-methylated isoflavonoidsCHEMONTID:0002604Isoflavonoids with methoxy groups attached to the C2' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
3'-O-methylated isoflavonoidsCHEMONTID:0002605Isoflavonoids with methoxy groups attached to the C3' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
4'-O-methylated isoflavonoidsCHEMONTID:0002606Isoflavonoids with methoxy groups attached to the C4' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.
2-phenylbenzofuransCHEMONTID:0002613Phenylbenzofurans where the benzofuran moiety is conjugated at the 2-position to a phenyl group.
Angular furanoflavonoids and dihydrofuranoflavonoidsCHEMONTID:0002615Flavonoids possessing a furan (or a dihydrofuran) ring angularly fused to the benzopyran moiety of the flavonoid skeleton.
Linear furanoflavonoids and dihydrofuranoflavonoidsCHEMONTID:0002616Flavonoids possessing a furan (or a dihydrofuran) ring linearly fused to the benzopyran moiety of the flavonoid skeleton.
Tetrahydropteroic acids and derivativesCHEMONTID:0003042Heterocyclic compounds based on the 5,6,7,8-tetrahydropteroic acid skeleton (or derivative thereof).
Dihydropteroic acids and derivativesCHEMONTID:0003041Dihydrogenated pteroic acids or derivatives thereof.
N-benzoylpiperidinesCHEMONTID:0002621Heterocyclic Compounds containing a piperidine ring conjugated to a benzyl group through one nitrogen ring atom.
N-benzylpiperidinesCHEMONTID:0002622Heterocyclic Compounds containing a piperidine ring conjugated to a benzyl group through one nitrogen ring atom.
PhenylsulfatesCHEMONTID:0002626Compounds containing a sulfuric acid group conjugated to a phenyl group.
2,4-disubstituted thiazolesCHEMONTID:0002634Compounds containing a thiazole ring substituted at the positions 2 and 3.
2,5-disubstituted thiazolesCHEMONTID:0002635Compounds containing a thiazole ring substituted at positions 2 and 5 only.
4,5-disubstituted thiazolesCHEMONTID:0002636Compounds containing a thiazole ring substituted at positions 4 and 5 only.
2,4,5-trisubstituted thiazolesCHEMONTID:0002637Compounds containing a thiazole ring substituted at positions 2, 4 and 5 only.
2,4-disubstituted oxazolesCHEMONTID:0002638Compounds containing an oxazole ring substituted at positions 2 and 4 only. Oxazole is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole.
2,5-disubstituted oxazolesCHEMONTID:0002639Compounds containing an oxazole ring substituted at positions 2 and 5 only. Oxazole is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole.
4,5-disubstituted oxazolesCHEMONTID:0002640Compounds containing an oxazole ring substituted at positions 4 and 5 only. Oxazole is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole.
2,4,5-trisubstituted oxazolesCHEMONTID:0002641Compounds containing an oxazole ring substituted at positions 2, 4 and 5 only. Oxazole is a five-membered aromatic heterocycle with one oxygen, one nitrogen, and three carbon atoms. Isomers include 1,2-oxazole and 1,3-oxazole.
6,7-dihydroxycoumarinsCHEMONTID:0002643Coumarins bearing two hydroxyl groups at positions 6 and 7 of the coumarin skeleton, respectively.
7,8-dihydroxycoumarinsCHEMONTID:0002644Coumarins bearing two hydroxyl groups at the C7- and C8-positions of the coumarin skeleton, respectively.
Lycoctonine alkaloidsCHEMONTID:0002678Alkaloids with a structure based on the hexacyclic lycoctonine skeleton, which contains a quinolizidine moiety, an azepane ring. Lycoctonine alkaloids are also characterized by the presence of an oxygenated group at the C7 carbon.
MolybdopterinsCHEMONTID:0002694Cofactors or analogs thereof, with a structure based on a furan ring fused to a pterin. In addition, the pyran ring features two thiolates, which serve as ligands in molybdo- and tungstoenzymes. In some cases, the alkyl phosphate group is replaced by an alkyl diphosphate nucleotide.
Phenylbenzo-1,3-dioxanesCHEMONTID:0002705Benzo-1,3-dioxanes having a phenyl group attached to the 1,3-dioxane moiety.
Phenylbenzo-2,3-dioxanesCHEMONTID:0002706Benzo-1,3-dioxanes having a phenyl group attached to the 2,3-dioxane moiety.
Phenylbenzo-1,4-dioxanesCHEMONTID:0002707Benzo-1,3-dioxanes having a phenyl group attached to the 1,4-dioxane moiety.
Solanocapsine-type alkaloidsCHEMONTID:0002725Steroidal alkaloids with a structure that is characterized by a docosahydronaphth[2,1:4',5']indene ring system fused to a pyrano[3,2-b]pyridine moiety.
Buxus alkaloidsCHEMONTID:0002726Alkaloids with a triterpenoid-steroid pregnane type structure with C-4 methyl groups, a 9beta,10beta-cycloartenol system, and a degraded C-20 side chain. Structurally, they are derivatives of either a 9beta,10beta-cyclo-4,4,14alpha-trimethyl-5alpha-pregnane or a 9(10->19)abeo 4,4,14alpha-trimethyl-5alpha-pregnane system.
Samamine-type alkaloidsCHEMONTID:0002727Alkaloids with a structure that is based on the samamine skeleton, a tetracyclic compound consisting of and azepane ring fuse a saturated cyclopenta[a]naphthalene derivative.
Jerveratrum-type alkaloidsCHEMONTID:0002728Steroidal alkaloids with a structure that is based on the jervane ring system. Jerveratrum alkaloids have alkamines with 1-3 oxygen atoms, and occur as such or as monoglycosides.
Cerveratrum-type alkaloidsCHEMONTID:0002729Steroidal alkaloids containing the cevane (23-methyl-4- azahexacyclo[12.11.0.0^{2,11}.0^{4,9}.0^{15,24}.0^{18,23}]pentacosane) moiety, which is a six ring system. Cerveratrum alkaloids have 7-9 oxygen atoms and occur as free alkamines or esters of simple aliphatic or aromatic acids.
Pregnane-type alkaloidsCHEMONTID:0002730Alkaloids with a structure based on the pregnane skeleton, which is characterized by the presence of monomethylamino or dimethylamino substituents either at C-3 and/or at the C-20 position in basic steroidal skeleton.
Conanine-type alkaloidsCHEMONTID:0002731Alkaloids with a structure based on the conanine skeleton.
22,26-epiminocholestanesCHEMONTID:0002732Steroid alkaloids obtained by reduction of spirosolane through opening of the E-ring.
22,23-secosolanidanes and derivativesCHEMONTID:0002733Cholestane derivatives that contain the 22,23-secosolanidane moiety. 22,23-secosolanidane arises from the conversion of the cholestane side-chain into a piperidine ring that is N-substituted with a 2-methylpropyl group.
3-aminospirostanesCHEMONTID:0002737Spirostane derivatives carrying an amino group at the 3-position. Spirostanes are 16b,22:22,26-diepoxycholestanes, or 22,26-epoxyfurostans. The sixth ring so formed is known as ring F.
Villanovane, atisane, trachylobane or helvifulvane diterpenoidsCHEMONTID:0003401Diterpenoids with a structure based on the villanovane, atisane, trachylobane or helvifulvane skeleton. The astisane and atisane skeletons arise from the rearrangement of the beyerane cation intermediate. The trachylobane and helvifulvane skeletons are formed by rearrangement of the beyerane cation intermediate followed by cyclisation.
Angular benzodifuransCHEMONTID:0002741Benzodifurans containing angularly fused benzene and furan rings.
Linear benzodifuransCHEMONTID:0002742Benzodifurans containing linearly fused benzene and furan rings.
Lysergic acidsCHEMONTID:0002745Derivatives of lysergic acid are amides in which the amidic moiety is formed by a small peptide or an alkylamide.
LysergamidesCHEMONTID:0002746Amides of Lysergic acids.
Pyridoxine-5'-phosphatesCHEMONTID:0002753Pyridoxines that carry a phosphate group at the 5-position.
AmidoximesCHEMONTID:0002760Amidines, in which the imino nitrogen is substituted by a hydroxy group.
IodophenolsCHEMONTID:0002763Halophenols carrying a iodine on the benzene ring.
BromophenolsCHEMONTID:0002764Halophenols carrying a bromine on the benzene ring.
FluorophenolsCHEMONTID:0002765Halophenols carrying a fluorine on the benzene ring.
ChlorophenolsCHEMONTID:0002766Halophenols carrying a chlorine on the benzene ring.
4-nitroquinoline N-oxidesCHEMONTID:0002779Nitroquinoline derivative bearing a nitro group at ring position 4 and N-oxide group at ring position 1.
ThianthrenesCHEMONTID:0002803Organic compounds containing a thianthrene moiety. Thianthrene is a tricyclic ring system that consists of two benzene rings fused to each other through a 1,4-dithiin ring.
Isoflav-3-enonesCHEMONTID:0002820Flavonoids with a structure based on an isoflav-3-ene skeleton bearing an oxo-group at position C2.
Ormosia-type alkaloidsCHEMONTID:0002825Aloperine alkaloids with a structure based on the ormosanine skeleton.
Pyrrolo[4,3,2-de]quinolinesCHEMONTID:0002829Organic heterocyclic compounds with a structure based on the Pyrrolo[4,3,2-de]quinoline skeleton.
PyrazolidinonesCHEMONTID:0002836Organic heterocyclic compounds containing a pyrazolidinone moiety.
Cyclic acetylenesCHEMONTID:0002846Cyclic hydrocarbons containing one or more acetylene groups.
Organic phosphoric acid monoamidesCHEMONTID:0002857Organophosphorus compounds with the general formula RNP(O)(O)=O (R=alkyl, aryl).
AzlactonesCHEMONTID:0002859Oxazol-5(4H)-ones I, compounds derived by cyclization of N-acyl alpha-amino carboxylic acids, RC(=O)NHCR2C(=O)OH, through formal loss of the elements of water.
GrayanoidsCHEMONTID:0002871Diterpenoids containing a skeleton based on or derived from the ent-kaurane moiety. Grayanoids usually possess either one of the grayanane, the 2,4-seco-grayanane, the 9,10-seco-grayanane, the 1,5-seco-grayanane, the kalmane, or the leucothane skeleton. Some derivatives also include the 1,5-seco-kalmane skeleton.
Elemane sesquiterpenoidsCHEMONTID:0002872Sesquiterpenoids with a structure based on the elemane skeleton. Elemane is a monocyclic compound consisting of a cyclohexane ring substituted with a methyl group, an ethyl group, and two 1-methylethyl groups at the 1-, 1-, 2-, and 4-position, respectively.
PseudoguaianesCHEMONTID:0002873Sesquiterpenoids with a structure based on the pseudoguaiane skeleton, which arises by the migration of the a methyl group of the bicyclic guaiane skeleton from the C4 to the C5 position.
GuaianesCHEMONTID:0002874Sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively.
Tigliane and ingenane diterpenoidsCHEMONTID:0002875Diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane.
Cyathane diterpenoidsCHEMONTID:0002876Fungal diterpenoid metabolites with a structure containing the cyathane skeleton (Tetradecahydro-3a,5a,8-trimethyl-1-(1-methylethyl)-cyclohept[e]indene).
Jatrophane and cyclojatrophane diterpenoidsCHEMONTID:0002877Diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton.
Xeniaphyllane and xenicane diterpenoidsCHEMONTID:0002879Diterpenoids with a structure based either on the xeniaphyllane or the xenicane skeleton.
Sphaerane diterpenoidsCHEMONTID:0002880Diterpenoids containing a sphaerane skeleton or tetradecahydro-5,8a,10a-trimethyl-1-(1-methylethyl)-phenanthrene.
Cheilanthane sesterterpenoidsCHEMONTID:0002881Sesterterpnoids with a structure based on the cheilanthane backbone. Cheilanthane is a tricyclic compound consisting of a tetradecahydrophenanthrene ring system that carries two methyl groups at the 1-position, one methyl group at the 4a-,7-, and 8a-positions, as well as a 3-methylpentyl group at the 8-position.
Ophiobolane sesterterpenoidsCHEMONTID:0002882Sesterterpnoids with a structure based on the ophiobolane backbone. Ophiobolane is a tricyclic compound consisting of two cyclopentane rings joined by a cyclooctane ring, and carries a methyl group at the 1-, 4-, and 8-position, as well as a 6-methylheptane group at the 12-position.
Scalarane sesterterpenoidsCHEMONTID:0002883Sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions.
Lupane triterpenoidsCHEMONTID:0002884Triterpenoids with a structure based on the lupane skeleton. They arise from the formation of a five membered ring E from the baccharane precursor.
Tirucallane and euphane triterpenoidsCHEMONTID:0002885Triterpenoids with a structure based either on the tirucallane or the euphane skeleton. They are obtained by backbone rearrangement of a dammarane-based precursor.
Taraxastane, ursane, and bauerane triterpenoidsCHEMONTID:0002886Triterpenoids with a structure based on either the taraxastane, ursane, or bauerane skeleton. These are obtained by methyl migration in ring E of the oleanane backbone.
Taraxerane, multiflorane, glutinane and friedelane triterpenoidsCHEMONTID:0002887Triterpenoids with a structure based either on the taraxerane, the multiflorane, the glutinane, or the friedelane skeleton. These compounds arise upon rearrangement of the oleanane skeleton.
Dammarane triterpenoidsCHEMONTID:0002888Triterpenoids with a structure based on the dammarane skeleton.
Protostane and fusidane triterpenoidsCHEMONTID:0002889Triterpenoids with a structure based either on the protostane or the fusidane skeleton.
Briarane diterpenoidsCHEMONTID:0002890Marine diterpenoids with a structure based on the briarane (3,8-cyclocembrane) skeleton.
M-quinoniminesCHEMONTID:0002893Quinonimines in which the imine groups are in a meta-relationship.
O-quinoniminesCHEMONTID:0002894Quinonimines in which the imine groups are in a ortho-relationship.
P-quinoniminesCHEMONTID:0002895Quinonimines in which the imine groups are in a para-relationship.
HomoisoflavanonesCHEMONTID:0002898Homoisoflavonoids with a structure based on the chromanone system. Chromanone is a bicyclic compound consisting of a 3,4-dihydro-1-benzopyran, which bears a ketone group at the 4-position.
1,2-dithiole-3-thionesCHEMONTID:0002905Organic heterocyclic compounds containing a 1,2-dithiole ring that bears a C=S group.
4-hydroxycoumarinsCHEMONTID:0002907Coumarins that contain one or more hydroxyl groups attached to C4-position the coumarin skeleton.
7-hydroxycoumarinsCHEMONTID:0002909Coumarins that contain one or more hydroxyl groups attached to the C7 position the coumarin skeleton.
Polypodane, malabaricane and podiodane triterpenoidsCHEMONTID:0002911Triterpenoids with a structure based either on the polypodane, the malabaricane, or the podiodane skeleton.
3-hydroxyflavonoidsCHEMONTID:0002914Flavonoids that bear one hydroxyl group at the C-3 position of the flavonoid skeleton.
3'-hydroxyflavonoidsCHEMONTID:0002915Flavonoids that bear one hydroxyl group at the C-3' position of the flavonoid skeleton.
Eunicellane and asbestinane diterpenoidsCHEMONTID:0002916Diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.
Arborinane and stictane triterpenoidsCHEMONTID:0002917Triterpenoids with a structure based on the arborinane or stictane skeleton.
Serratane and onocerane triterpenoidsCHEMONTID:0002918Triterpenoids with a structure based either on the serratane or the onocerane skeleton.
1,2,4-oxadiazolesCHEMONTID:0002924Compounds containing an oxadiazole ring with the oxygen and the two nitrogen atoms at positions 1, 2, and 4, respectively.
1,3,4-oxadiazolesCHEMONTID:0002925Compounds containing an oxadiazole ring with the oxygen and the two nitrogen atoms at positions 1, 3, and 4, respectively.
Aphidicolane and stemodane diterpenoidsCHEMONTID:0002931Diterpenoids with a structure based on the aphidicolane or the stemodane skeleton.
Long-chain fatty acidsCHEMONTID:0002949Fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
Very long-chain fatty acidsCHEMONTID:0002950Fatty acids with an aliphatic tail that contains at least 22 carbon atoms.
Long-chain fatty alcoholsCHEMONTID:0002951Fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.
Long-chain fatty aldehydesCHEMONTID:0002952Fatty aldehydes carrying a long aliphatic chain, with 13 to 21 carbon atoms.
SulfonohydrazidesCHEMONTID:0002959Organic compounds with the general formula RS(=O)(=O)NHNH2.
N-acylsphingosinesCHEMONTID:0002961Sphingolipids containing a N-acylated sphingosine.
N-acylsphinganinesCHEMONTID:0002962Sphingolipids containing a N-acylated sphinganine.
PhytoceramidesCHEMONTID:0002963N-acylated 4-hydroxysphinganine.
3-hydroxysteroidsCHEMONTID:0003027Steroids carrying a hydroxyl group at the 3-position of the steroid backbone.
3-oxosteroidsCHEMONTID:0003026Steroid derivatives carrying a C=O group at the 3-position of the steroid skeleton.
N-acyl-phenylthioureasCHEMONTID:0002981Thiourea derivatives where one nitrogen atom of the urea group is linked to a phenyl group and the other is acylated.
N-acyl-phenylureasCHEMONTID:0002982Urea derivatives where one nitrogen atom of the urea group is linked to a phenyl group and the other is acylated.
AcylguanidinesCHEMONTID:0002983N-acylated derivatives of guanidines.
6-aminopurinesCHEMONTID:0002987Purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
4-hydroxyflavonoidsCHEMONTID:0002988Flavonoids that bear one hydroxyl group at the C-4 position of the flavonoid skeleton.
4'-hydroxyflavonoidsCHEMONTID:0002989Flavonoids that bear one hydroxyl group at the C-4' position of the flavonoid skeleton.
6-hydroxyflavonoidsCHEMONTID:0002990Flavonoids that bear one hydroxyl group at the C-6 position of the flavonoid skeleton.
5-hydroxyflavonoidsCHEMONTID:0002992Flavonoids that bear one hydroxyl group at the C-5 position of the flavonoid skeleton.
7-hydroxyflavonoidsCHEMONTID:0002993Flavonoids that bear one hydroxyl group at the C-7 position of the flavonoid skeleton.
8-hydroxyflavonoidsCHEMONTID:0002994Flavonoids that bear one hydroxyl group at the C-8 position of the flavonoid skeleton.
Alpha-halocarboxylic acidsCHEMONTID:0003000Carboxylic acids containing a halogen atom bonded to the alpha carbon atom.
Alpha-halocarboxylic acid derivativesCHEMONTID:0003001Carboxylic acid derivatives containing a halogen atom bonded to the alpha carbon atom.
MonohydroxyflavonoidsCHEMONTID:0003006Flavonoids that bear one hydroxyl group on the flavonoid skeleton.
Flavan-4-olsCHEMONTID:0003013Flavans that bear and hydroxyl group at position 4 (B ring), but not at the 3-position.
Polyprenylbenzene-1,2-diolsCHEMONTID:0003028Compounds containing a polyisoprene chain attached to a catechol group.
Pyrrolidine-2-onesCHEMONTID:0003031Pyrrolidines which bear a C=O group at position 2 of the pyrrolidine ring.
Pyrrolidine-3-onesCHEMONTID:0003032Pyrrolidines which bear a C=O group at position 3 of the pyrrolidine ring.
C-nitroso compoundsCHEMONTID:0003034Nitroso compounds with he general formula RN=O, where R is an organic group.
25-azasteroids and derivativesCHEMONTID:0003053Azasteroids where the carbon atom at position 25 is replaced by a nitrogen atom.
8-azasteroids and derivativesCHEMONTID:0003054Azasteroids where the carbon atom at position 8 is replaced by a nitrogen atom.
6-azasteroids and derivativesCHEMONTID:0003055Azasteroids where the carbon atom at position 6 is replaced by a nitrogen atom.
4-azasteroids and derivativesCHEMONTID:0003056Azasteroids where the carbon atom at position 4 is replaced by a nitrogen atom.
p-BromobenzenesulfonatesCHEMONTID:0003057Benzenesulfonic acids (or derivative thereof) carrying a bromine at the para- position.
20-oxosteroidsCHEMONTID:0003058Steroid derivatives carrying a C=O group at the 20-position of the steroid skeleton.
11-oxosteroidsCHEMONTID:0003059Steroid derivatives carrying a C=O group at the 11-position of the steroid skeleton.
16-oxosteroidsCHEMONTID:0003060Steroid derivatives carrying a C=O group at the 16-position of the steroid skeleton.
CarbapenamsCHEMONTID:0003066Beta-lactams with a saturated carbapenem skeleton.
GlycosyldiradylglycerolsCHEMONTID:0003822Glycosylglycerols that carry exactly two acyl chains attached to the glycerol moiety.
1,8-naphthalic anhydridesCHEMONTID:0003071Organic aromatic compounds that contain a naphthalene carrying two carboxyl groups at the 1- and 8-positions. In naphthalene anhydrides, the two carboxyl groups at the 1- and 8-positions share one oxygen atom.
1-carboxy-2-haloaromatic compoundsCHEMONTID:0003072Aromatic compounds containing 1 carboxyl group and a C-X (X = halogen) group at adjacent positions of an aromatic ring.
Aromatic alcoholsCHEMONTID:0003073Compounds containing an alcohol group attached to an aromatic carbon.
AldoximesCHEMONTID:0003078Organic compounds with the general formula RC(H)=NOH (R = organyl).
KetoximesCHEMONTID:0003079Organic compounds with the general formula RC(R')=NOH (R,R' = organyl).
N-aliphatic s-triazinesCHEMONTID:0003080N-aliphatic amine derivatives of 1,3,5-triazines. 1,3,5-triazines are aromatic compounds having three nitrogen ring atoms at the 1-, 3-, and 5- positions.
Acylsulfonic acids and derivativesCHEMONTID:0003081Acylated products of sulfonic acids (or derivatives).
2-polyprenyl-6-methoxyphenolsCHEMONTID:0003083Compounds containing a polyisoprene chain attached at the 2-position of a 6-methoxyphenol group.
Peroxybenzoic acids and derivativesCHEMONTID:0003085Organic compounds with a structure containing a benzoic acid or a derivative thereof.
Medium-chain fatty acidsCHEMONTID:0003086Fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
2-benzylpiperidinesCHEMONTID:0003088Organic compounds containing a benzyl group attached to the 2-position of a piperidine.
3-benzylpiperidinesCHEMONTID:0003089Organic compounds containing a benzyl group attached to the 3-position of a piperidine.
4-benzylpiperidinesCHEMONTID:0003090Organic compounds containing a benzyl group attached to the 4-position of a piperidine.
N-acyliminesCHEMONTID:0003091N-acyl derivatives of imines. Imines are compounds containing an imine functional group, with the general structure RN=CR2 (R = H, hydrocarbyl).
21-hydroxysteroidsCHEMONTID:0003095Steroids carrying a hydroxyl group at the 21-position of the steroid backbone.
Halobenzoic acids and derivativesCHEMONTID:0003096Benzoic acids or derivatives carrying a halogen atom on the benzene ring.
Seleninyl compoundsCHEMONTID:0003119Organic compounds with the general formula RSe(=O)R' (R = organyl).
Selenonyl compoundsCHEMONTID:0003120Organoselenium compounds with the general formula RSe(=O)(=O)R'
Telluronyl compoundsCHEMONTID:0003121Orgnotellurium compounds with the general formula R[Te](R')(=O)=O (R = organyl, R' not O-atom).
Tellurinyl compoundsCHEMONTID:0003122Organotellurium compounds with the general formula RTe(=O)R' (R = organyl).
Selenocarbonyl compoundsCHEMONTID:0003123Organoselenium compounds with the general formula RC(=Se)R' (R= organyl, R' = H, organyl).
Tellurocarbonyl compoundsCHEMONTID:0003124Organotellurium compounds with the general formula RC(=Te)R' (R= organyl, R' = H, organyl).
Hydrazinecarboxylic acidsCHEMONTID:0003133Organonitrogen compounds with the general formula RN(H)N(H)C(=O)OH (R = organyl).
HydrazinecarboxamidesCHEMONTID:0003134Organonitrogen compounds with the general formula RN(H)N(H)C(=O)N (R = organyl).
AlkoxysilanesCHEMONTID:0003265Organosilicon compounds with the general formula RO[Si](OR')(R'')(R''') (R,R' = organyl; R'',R''' = any atom).
Very long-chain fatty aldehydesCHEMONTID:0003174Fatty aldehydes carrying a long aliphatic chain, with at least 22 carbon atoms.
Enoyl CoAsCHEMONTID:0003180Organic compounds containing a coenzyme A substructure linked to an acyl chain.
Glycero-3-phospho-N-acyl-ethanolaminesCHEMONTID:0003187Glycerophosphoethanolamines with a n-acylated ethanolamine moiety.
Acyl homoserinesCHEMONTID:0003188N-acylated homoserine derivatives.
Ammonium ylidesCHEMONTID:0003192Organonitrogen compounds with the general formula R3N+-C-R2.
AlkylsilanesCHEMONTID:0003195Aliphatic organosilicon compounds.
AlkylarylsilanesCHEMONTID:0003196Organosilicon compounds with the general formula R[Si]R' (R = alkyl, R' = aryl).
Alpha-diazo estersCHEMONTID:0003197Organonitrogen compounds with the general formula ROC(=O)C=[N+]=[N-] (R = organyl).
Alpha-diazo ketonesCHEMONTID:0003198Organonitrogen compounds with the general formula RC(=O)C=[N+]=[N-] (R = organyl).
Silyl ethersCHEMONTID:0003200Organic compounds containing a silicon atom covalently bonded to an alkoxy group. They have the general formula R1R2R3Si-O-R4 (R4 = aryl, alkyl).
SilanolsCHEMONTID:0003201Organosilicon compounds with the general formula R[Si]OH (R = organyl group).
MaleimidesCHEMONTID:0003203Compounds containing a 2,5-pyrroledione moiety.
2,3-dihydro-4-pyridonesCHEMONTID:0003204Organic compounds containing a 2,3-dihydrogenated derivative of 4-pyridone.
SiloxanesCHEMONTID:0004446Saturated silicon-oxygen hydrides with unbranched or branched chains of alternating silicon and oxygen atoms (each silicon atom is separated from its nearest silicon neighbours by single oxygen atoms). The general structure of unbranched siloxanes is H3Si[OSiH2]nOSiH3. H3Si[OSiH2]nOSiH[OSiH2OSiH3]2 is an example of a branched siloxane. By extension hydrocarbyl derivatives are commonly included.
2-phenylindolesCHEMONTID:0003214Indoles substituted at the 2-position with a phenyl group.
2-amino-3-aroylthiophenesCHEMONTID:00032173-aroylthiophenes which are substituted by an amino group at the 2-position.
11-hydroxysteroidsCHEMONTID:0003228Steroids carrying a hydroxyl group at the 11-position of the steroid backbone.
16-hydroxysteroidsCHEMONTID:0003229Steroids carrying a hydroxyl group at the 16-position of the steroid backbone.
17-hydroxysteroidsCHEMONTID:0003236Steroids carrying a hydroxyl group at the 17-position of the steroid backbone.
7-hydroxysteroidsCHEMONTID:0003238Steroids carrying a hydroxyl group at the 7-position of the steroid backbone.
12-hydroxysteroidsCHEMONTID:0003241Steroids carrying a hydroxyl group at the 12-position of the steroid backbone.
7-oxosteroidsCHEMONTID:0003244Steroid derivatives carrying a C=O group at the 7-position of the steroid skeleton.
6-oxosteroidsCHEMONTID:0003249Steroid derivatives carrying a C=O group at the 6-position of the steroid skeleton.
17-azasteroids and derivativesCHEMONTID:0003253Azasteroids where the carbon atom at the25 position is replaced by a nitrogen atom.
(2R)-hydroxy acids and derivativesCHEMONTID:00032542R-enantiomers of alpha hydroxy acids and derivatives thereof.
3-O-beta-D-monogalactosyl-sn-glycerolsCHEMONTID:0003345Glycosylglycerols carrying a beta-D-galactose at the 3-position of the glycerol moiety.
MonoalkylglycerolsCHEMONTID:0003263Glycerolipids containing exactly one aliphatic chain linked to the glycerol moiety. This chain is the only one linked to the glycerol.
AlkylhalosilanesCHEMONTID:0003273Organosilicon compounds with the general formula R(Si(R')(R\"))nX (R = aliphatic chain, R'-R\" =H, C, or halogen atom, X = halogen atom).
Tosyl compoundsCHEMONTID:0003276Organosulfur compounds containing a tosyl group, with the general formula CH3C6H4S(O2)R (R = any atom).
p-NitrobenzenesulfonatesCHEMONTID:0003277Benzenesulfonic acids (or derivative thereof) carrying a nitro group at the para- position.
p-MethylbenzenesulfonatesCHEMONTID:0003278Benzenesulfonic acids (or derivative thereof) carrying a methyl group at the para- position.
N-hydroxyguanidinesCHEMONTID:0003280Compounds containing a guanidine group in which one of the hydrogens attached to the nitrogen at position 1 is substituted by a hydroxyl group.
Miscellaneous metavanadatesCHEMONTID:0003289Inorganic compounds in which the largest metallic oxoanion is metavanadate, to which either no atom or a non metal atom is bonded.
Naphthalene sulfonatesCHEMONTID:0003310Organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
Pyridyl-1,2,3-triazolesCHEMONTID:0003318Organic compounds containing a pyridine ring attached to a 1,2,3-triazole ring.
Pyridyl-1,2,4-triazolesCHEMONTID:0003319Organic compounds containing a pyridine ring attached to a 1,2,4-triazole ring.
1,2-diacylglycero-3-phosphosulfocholinesCHEMONTID:0003321Glycerophosphosulfocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
2,3-dienoyl fatty acyl thioestersCHEMONTID:0003328Thioesters of a 2,3-dienoyl fatty acid with the general formula RC(=O)SR', where R is the fatty acyl chain.
3-O-beta-D-digalactosyl-sn-glycerolsCHEMONTID:0003344Glycosylglycerols carrying a beta-D-digalactose at the 3-position of the glycerol moiety.
1,2,3-oxadiazolesCHEMONTID:0003351Compounds containing an oxadiazole ring with the oxygen and the two nitrogen atoms at positions 1, 2, and 3, respectively.
2-aminothieno[3,4-c]pyridazinesCHEMONTID:0003355Organic compounds containing a thieno[3,4-c]pyridazine that carries an amino group at the 2-position. Thieno[3,4-c]pyridazine is a bicyclic compound made up of a thiophene ring fused to a pyridazine ring so that the sulfur atom and the two nitrogen atoms are at the 1-, 5-, and 6-position, respectively.
2-aminothieno[3,4-d]pyridazinesCHEMONTID:0003356Organic compounds containing a thieno[3,4-d]pyridazine that carries an amino group at the 2-position. Thieno[3,4-d]pyridazine is a bicyclic compound made up of a thiophene ring fused to a pyridazine ring so that the sulfur atom and the two nitrogen atoms are at the 1-, 4-, and 5-position, respectively.
N-alkylpiperazinesCHEMONTID:0003357Organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group.
N-arylpiperazinesCHEMONTID:0003359Organic compounds containing a piperazine ring where the nitrogen ring atom carries an aryl group.
30-hydroxysteroidsCHEMONTID:0003360Steroids carrying a hydroxyl group at the 30-position of the steroid backbone.
1-aminopyrazinium compoundsCHEMONTID:0003362Organic compounds containing a pyrazinium ring that carries an amine group at the 1-position.
2-aminopyrazinium compoundsCHEMONTID:0003363Organic compounds containing a pyrazinium ring that carries an amine group at the 2-position.
3-carboxy steroidsCHEMONTID:0003368Steroid compounds that carry a carboxyl group at the C3-atom of the steroid backbone.
17-carboxy steroidsCHEMONTID:0003369Steroid compounds that carry a carboxyl group at the C17-atom of the steroid backbone.
1,2-dithiolanecarboxylic acidsCHEMONTID:0003379Organic compounds containing a 1,2-dithiolane ring that bears one or more carboxylic acid groups. The 1,2-dithiolane moiety is a 5-membered ring with three carbon atoms, and two sulfur atoms at the 1- and 2- ring positions.
1,3-dithiolanecarboxylic acidsCHEMONTID:0003380Organic compounds containing a 1,3-dithiolane ring that bears one or more carboxylic acid groups. The 1,3-dithiolane moiety is a 5-membered ring with three carbon atoms, and two sulfur atoms at the 1- and 3- ring positions.
alpha-Mercaptocarboxylic acidsCHEMONTID:0003381Carboxylic acids that bear a thiol group at the C-2 position. Alpha-mercaptocarboxylic acids have the general formula RC(S)C(=O)O, where R = H, organyl group.
Thiophosphate monoestersCHEMONTID:0003382Organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where exactly one R-group is an organyl group.
Thiophosphate diestersCHEMONTID:0003383Organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where exactly two R-groups are organyl groups.
Thiophosphate triestersCHEMONTID:0003384Organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where exactly three R-groups are organyl groups.
1'-(acyl-sn-glycero-3-phospho),3'-(acyl-sn-glycero-3-phospho)-sn-glycerolsCHEMONTID:0003388Glycerophospholipids in which the O1 and O3 oxygen atoms of the central glycerol moiety are each linked to one 1-monoacylglyerol chain.
5'-phospho-(3'->5')-dinucleotidesCHEMONTID:0003396(3'->5')-dinucleotides in which one of the based bears a phosphate group (or a phosphate chain) at the 5'-position.
Sphenolobane diterpenoidsCHEMONTID:0003397Diterpenoids with a structure characterized by a sphenolobane skeleton. They possess a trans-fused hydroazulenoid skeleton as a common structural motif, but differ in configuration at C(9), where a prenyl group is attached. Sphenolobane is also considered an 'extended' daucane skeleton, with a carbon side chain appended onto the cyclopentane ring.
Amphilectane, neoamphilectane, cycloamphilectane, and adociane diterpenoidsCHEMONTID:0003398Diterpenoids with a structure based on the amphilectane or a seco-,neo-, or cyclo- derivative thereof. Amphilectane is a tricyclic structure made up of three cyclohexane fused together, with a methyl group at the C11-, C7-, and C3- positions. Additionally, it carries a 2-methylpropyl group at the C1-position. Amphilectanes are presumably derived from serrulatanes. Cycloamphilectanes represent a further cyclisation.
Cyclohexane sesterterpenesCHEMONTID:0003399Sesterterpenoids with a structure containing a cyclohexane linked to an isoprenyl chain. They arise by cyclisation of the acyclic sesterterpene skeleton between carbons 14 and 19.
Fatty acid methyl estersCHEMONTID:0003417Compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group.
Alpha-acyloxy carbonyl compoundsCHEMONTID:0003677Carbonyl compounds that have an acyloxy substituent alpha to the carbonyl group. They have the general structure R4C(=O)OC(R2)(R3)C(R1)=O (R1,R4=H or organyl; R2,R3 = any atom).
7,8'-epoxylignansCHEMONTID:0003421Lignans that contain either isomer of the 7,8'-epoxylignan skeleton. The first isomer consists of a tetrahydrofuran that carries a phenyl group at the 2- and the 4-positions, as well as one a methyl group at the 3- and 5-positions. The second isomer consists of a tetrahydrofuran that carries a benzyl group, a phenyl group, and a methyl group at the 2-, 4-, 5-position, respectively.
7,9'-epoxylignansCHEMONTID:0003422Lignans that contain the 7,9'-epoxylignan skeleton, which consists of a tetrahydrofuran that carries a phenyl group, a methyl group, and a benzyl group at the 2-, 3-, 4-position, respectively.
7,7'-epoxylignansCHEMONTID:0003423Lignans with a structure based on a 2,5-diaryl-3, 4-dimethyltetrahydrofuran skeleton.
Croomine-type alkaloidsCHEMONTID:0003428Stemona alkaloids with a structure containing a pyrrolo[1,2-a]azepine group, where the azepine moiety forms a spiro system with oxolane-5-one to give spiro[oxolane-2,9'-pyrrolo[1,2-a]azepine]-5-one. Moreover, another 5-oxooxolane moiety attached to the pyrrole ring.
Stichoneurine-type alkaloidsCHEMONTID:0003429Stemona alkaloids with a structure that typically contains a 3-methyloxolan-2-one and a 5-propyloxolan-2-one moieties that are attached to the characteristic pyrrolo[1,2-a]azepine skeleton at the C3 and C9 position, respectively.
Protostemonine-type alkaloidsCHEMONTID:0003430Stemona alkaloids with a structure containing a pyrrolo[1,2-a]azepine skeleton (S1) , one 5-oxooxolane moiety (S2), and one a 5-(oxolan-2-yl)oxolan-2-one moiety (S3). The S2 moiety is linked to the C3 atom of the pyrrole ring in the S1 moiety. Additionally, the azepine ring of S1 is fused to one oxolane ring of the S3 moiety.
Dithiocarboxylic acidsCHEMONTID:0003437Organic compounds with the general formula RC(=S)SH.
Dithiocarboxylic acid amidesCHEMONTID:0003438Organic compounds with the general formula RC(=S)SN(R')R'', (R = organyl group; R', R'' = H, organyl group.
Dithiocarboxylic acid estersCHEMONTID:0003439Organic compounds with the general formula RC(=S)SR', where R and R' are organyl groups.
6-thiopurinesCHEMONTID:0003453Compounds containing a purine that carries a thiol group at the 6-position. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
Alkyl phosphatesCHEMONTID:0003457Organic compounds containing a phosphate group that is linked to one or more alkyl chains.
Alkanesulfinic acidsCHEMONTID:0003462Organosulfur compounds containing an aliphatic group attached to a sulfinic acid group (or a derivative thereof), with the general formula RSO2R' (R= alkyl, R'=H).
2'-HydroxychalconesCHEMONTID:0003472Organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.
2'-Hydroxy-dihydrochalconesCHEMONTID:0003473Organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position.
RetrochalconesCHEMONTID:0003474A form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
Retro-dihydrochalconesCHEMONTID:0003475A form of normal dihydrochalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
2,3-CyclopentanoindolinesCHEMONTID:0003476Organic aromatic compounds containing an indoline ring system that shares its C2-C3 bond with a cyclopentane ring.
C-cinnamoyl glycosidesCHEMONTID:0003478C-glycoside derivatives of cinnamic acid. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid.
O-cinnamoyl glycosidesCHEMONTID:0003479O-glycoside derivatives of cinnamic acid. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid.
Angular pyranocoumarinsCHEMONTID:0003485Organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety.
Linear pyranocoumarinsCHEMONTID:0003486Organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety.
2,4-diphenylfuransCHEMONTID:0003488Organic heterocyclic compounds that contain a furan ring substituted with a phenyl group only the C2- and C4-positions.
2,5-diphenylfuransCHEMONTID:0003489Organic heterocyclic compounds that contain a furan ring substituted with a phenyl group only the C2- and C5-positions.
3,4-diphenylfuransCHEMONTID:0003490Organic heterocyclic compounds that contain a furan ring substituted with a phenyl group only the C3- and C4-positions.
4-carboxy steroidsCHEMONTID:0003492Steroid compounds that carry a carboxyl group at the C4-atom of the steroid backbone.
PyranochromenesCHEMONTID:0003543Organic heterocyclic compounds containing a pyran ring fused to a chromene (1-benzopyran) moiety.
Rhamnofolane and daphnane diterpenoidsCHEMONTID:0003494Diterpenoids with a structure based on one the rhamnofolane or daphnane skeleton. The rhamnofolane and daphnane skeletons are closely related, being formally derived from casbane by two cyclizations (6,10 and 5,14) followed by cleavage of the 1,15 (daphnane) or 2,15 (rhamnofolane) cyclopropane bonds.
3-prenylated flavonesCHEMONTID:0003501Flavones that features a C5-isoprenoid substituent at the 3-position.
3'-prenylated flavonesCHEMONTID:0003502Flavones that features a C5-isoprenoid substituent at the 3'-position.
6-prenylated flavonesCHEMONTID:0003503Flavones that features a C5-isoprenoid substituent at the 6-position.
8-prenylated flavonesCHEMONTID:0003504Flavones that features a C5-isoprenoid substituent at the 8-position.
3-prenylated flavansCHEMONTID:0003639Flavans that features a C5-isoprenoid substituent at the 3-position.
3'-prenylated flavansCHEMONTID:0003643Flavans that features a C5-isoprenoid substituent at the 3'-position.
6-prenylated flavansCHEMONTID:0003646Flavans that features a C5-isoprenoid substituent at the 6-position.
8-prenylated flavansCHEMONTID:0003642Flavans that features a C5-isoprenoid substituent at the 8-position.
3-prenylated chalconesCHEMONTID:0003509Chalcones featuring a C5-isoprenoid unit at the 3-position.
3'-prenylated chalconesCHEMONTID:0003510Chalcones featuring a C5-isoprenoid unit at the 3'-position.
2,2-dimethyl-1-benzopyransCHEMONTID:0003522Organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.
Meta,para-diphenylether diarylheptanoidsCHEMONTID:0003523Cyclic diarylheptanoids where the two benzene rings are linked to each other by an ether group conjugated to the 3-position of one benzene ring and the 4-position of the other ring.
Meta,meta-bridged biphenylsCHEMONTID:0003524Cyclic diarylheptanoids where the two aryl groups are linked to each other by an ether group conjugated to their 3-position.
RotenonesCHEMONTID:0003528Rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton.
Dinaphtho[2,1-b;2',3'-d]furansCHEMONTID:0003537Organic aromatic compounds that contain two naphthalene moieties fused to each other through a furan ring to form a dinaphtho[2,1-b;2',3'-d]furan skeleton.
FuranochalconesCHEMONTID:0003542Compounds containing a furan ring fused to either ring of a chalcone moiety.
Himachalane and lippifoliane sesquiterpenoidsCHEMONTID:0003545Diterpenoids with a structure based on either the himachalane or the lippifoliane skeleton.
Jatropholane and crotopholane diterpenoidsCHEMONTID:0003546Diterpenoids with a structure based either on the jatropholane or the crotopholane skeleton. Jatropholanes arise by 5,13- and 6,10-cyclisation of a casbane precursor. Subsequent cleavage of the 2,15-cyclopropane bond affords crotofolane.
Fusicoccane diterpenoidsCHEMONTID:0003547Diterpenoids with a structure based on a 20-carbon dicyclopenta[a,d]cyclooctane skeleton (5->8->5 ring system) known as fusicoccane.
Valparane and mulinane diterpenoidsCHEMONTID:0003548Diterpenoids with a structure based on either the valparane or mulinane skeleton. Valparane and mulinane are tricyclic compounds containing a tetradecahydrocyclohepta[e]indene skeleton. Valparane carries a 1-methylethyl at the 3-position, as well as three methyl groups at the 5a-, 8-, and 10b-position of the ring system. Mulinane carries a 1-methylethyl at the 3-position, as well as three methyl groups at the 3a-, 5a-, and 8-position of the ring system.
Bicyclogermacrane and isolepidozane sesquiterpenoidsCHEMONTID:0003549Sesquiterpenoids with a structure based either on the bicyclogermacrane (3,7,11,11-tetramethylbicyclo[8.1.0]undecane, 9CI) skeleton or the isolepidozane skeleton.
Pachydictyane and cneorubin diterpenoidsCHEMONTID:0003550Diterpenoids with a structure that is based either on the pachydictyane or the cneorubin skeleton. Pachydictyane is a bicyclic compound consisting of a guaiane skeleton that carries a prenyl group attached to the C12 carbon atom. Cneorubin is a tricyclic compound consisting of a cycloprop[e]azulene where the cyclopropane carries a methyl group and a 4-methylpentyl group.
19-oxosteroidsCHEMONTID:0003557Steroid derivatives carrying a C=O group at the 19-position of the steroid skeleton.
17-oxosteroidsCHEMONTID:0003558Steroid derivatives carrying a C=O group at the 17-position of the steroid skeleton.
Elisabethane diterpenoidsCHEMONTID:0003559Diterpenoids with a structure based on the elisabethane skeleton, a tricyclic serrulatane derivative that is formed by connecting the C1 and C9 atom of serrulatane. This class of compounds also includes seco-elisabethane derivatives, nor-elisabethanes (resulting from the loss of one carbon atom), and bisnor-elisabethanes (resulting from the loss of two carbon atoms).
Elisapterane, elisabane, cumbiane or colombiane diterpenoidsCHEMONTID:0003560Diterpenoids with a structure based on either the elisapterane, elisabane, cumbiane or colombiane skeleton. They derive from serrulatane. Elisapterane is a tetracyclic compound formed by C10-C15 cyclization of elisabethane. Elisabane (nor-elisapterane) results from the loss of the C17 carbon atom of elisapterane. Cumbiane is formed by C10-C16 cyclization of the elisabethane carbon skeleton. Meanwhile, the cleavage of the C15-C16 bond of cumbiane yields the seco-cumbiane skeleton. Colombiane is also a tetracyclic skeleton arises from the C12-C2 cyclization of the elisabethane skeleton.
Ileabethane, pseudopterane or nor-sandresane diterpenoidsCHEMONTID:0003561Diterpenoids with a structure based on either the ileabethane, the pseudopterane, or the nor-sandresane skeleton. Ileabethane is a tricyclic carbon skeleton arising from the C8-C14 of serrulatane. In the nor-sandresane skeleton, a cyclohexane ring is fused to a seven-membered saturated aliphatic carbocycle, which could stem from the rearrangement of an amphilectane-based precursor involving loss of a carbon atom and a 1,2-alkyl shift with ring expansion.
Rotundane sesquiterpenoidsCHEMONTID:0003563Sesquiterpenoids with a structure based on the rotundane skeleton, which arise by a C10-C12 cyclization of bicyclic guaiane skeleton.
Aristolane sesquiterpenoidsCHEMONTID:0003565Sesquiterpenoids with a structure based on the aristolane skeleton. Aristolanes arise from the C6,C11 cyclization of the bicyclic eremophilane skeleton.
Estrogens and derivativesCHEMONTID:0003570Steroids with a structure containing a 3-hydroxylated estrane.
6-hydroxysteroidsCHEMONTID:0003578Steroids carrying a hydroxyl group at the 6-position of the steroid backbone.
Precapnellane sesquiterpenoidsCHEMONTID:0003584Sesquiterpenes with a structure characterized by the presence of a precapnellane skeleton. Precapnellane is a bicyclic compound made up of a cyclopentane fused to a cyclooctane and carrying one methyl group at the 1- and 5-position, as well as two methyl groups at the 8-position.
2'-prenylated flavonesCHEMONTID:0003587Flavones that features a C5-isoprenoid substituent at the 2'-position.
2'-prenylated flavansCHEMONTID:0003645Flavans that features a C5-isoprenoid substituent at the 2'-position.
Naphthalene sulfonamidesCHEMONTID:0003593Organic aromatic compounds that contain a naphthalene moiety that carries a sulfonamide (or a derivative thereof) at one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
1-naphthalene sulfonic acids and derivativesCHEMONTID:0003598Organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group (or a derivative thereof) at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
2-naphthalene sulfonic acids and derivativesCHEMONTID:0003599Organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group (or a derivative thereof) at the 2-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
2-bromoanilinesCHEMONTID:0003602Organic compounds that contain an aniline carrying a bromine atom at the C2-position.
1,2-dihalobenzenesCHEMONTID:0003664Organic compounds that contain a benzene ring that is substituted by halogen atoms at exactly two carbon atoms, which are adjacent.
Ceramide 2-N-methylaminoethylphosphonatesCHEMONTID:0003604Phosphonosphingolipids consisting of a ceramide skeleton, which conjugated to the phosphonate moiety of a N-methyl linked 2-aminoethylphosphonate group.
Ceramide aminoethylphosphonatesCHEMONTID:0003605Phosphonosphingolipids consisting of a ceramide skeleton, which conjugated to a 2-aminoethylphosphonate group.
Thio-lactosylceramidesCHEMONTID:0003606Glycosphingolipids with a structure containing a ceramide skeleton that is S-glycosidically linked to a lactose moiety.
Glycerol-3-phosphonoethanolaminesCHEMONTID:0003618Lipids that contain a phosphonoethanolamine group linked to the C3 terminal carbon of a glycerol moiety.
Glycerol-3-phosphonocholinesCHEMONTID:0003617Lipids that contain a phosphonocholine group linked to the C3 terminal carbon of a glycerol moiety.
Carbonyl ylidesCHEMONTID:00036221,3-Dipolar Compounds having the general structure R1C(R2)=[O+][C-](R3)R4 or R1[C+](R2)O[C-](R3)R4.
1,2-dithiole-3-onesCHEMONTID:0003623Organic heterocyclic compounds containing a 1,2-dithiole ring that bears a C=O group.
3-prenylated flav-3-enesCHEMONTID:0003638Flav3-enes that features a C5-isoprenoid substituent at the 3-position.
4-prenylated flavansCHEMONTID:0003640Flavans that features a C5-isoprenoid substituent at the 4-position.
7-prenylated flavansCHEMONTID:0003641Flavans that features a C5-isoprenoid substituent at the 7-position.
4'-prenylated flavansCHEMONTID:0003644Flavans that features a C5-isoprenoid substituent at the 4'-position.
Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoidsCHEMONTID:0003655Sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.
Organic phosphoric acid diamidesCHEMONTID:0003662Organophosphorus compounds with the general formula RNP(R2)(O)=O (R=alkyl, aryl; R2 = amine group).
1,3-dihalobenzenesCHEMONTID:0003665Organic compounds that contain a benzene ring that is substituted by halogen atoms at exactly two carbon atoms, C1 and C3, respectively.
1,4-dihalobenzenesCHEMONTID:0003666Organic compounds that contain a benzene ring that is substituted by halogen atoms at exactly two carbon atoms, C1 and C4, respectively.
ThioflavonesCHEMONTID:0003682Organic compounds that contains the 2-phenyl-4H-1-benzothiopyran-4-one skeleton, which consists of a 1-benzothiopyran-4-one substituted at the 2-position by a phenyl group. These compounds are thio analogues of flavones.
TyrosolsCHEMONTID:0003698Organic aromatic compounds containing a phenethyl alcohol moiety that carries a hydroxyl group at the 4-position of the benzene group.
1,2-substituted cyclopentyl nucleosidesCHEMONTID:0003739Nucleoside analogues with a structure that consists of a cyclopentane that is substituted a the 1-position with a hydroxyl group and at the 2-position with either a purine or pyrimidine base.
1,3-substituted cyclopentyl nucleosidesCHEMONTID:0003740Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine or pyrimidine base.
Cyclopropyl purine nucleosidesCHEMONTID:0003721Nucleoside analogues with a structure that consists of a cyclopropane that is substituted a the 1-position with a hydroxyl group and at the 2- position with either a purine base.
Cyclopropyl pyrimidine nucleosidesCHEMONTID:0003722Nucleoside analogues with a structure that consists of a cyclopropane that is substituted a the 1-position with a hydroxyl group and at the 2- position with either a pyrimidine base.
Phosphonated cyclopropyl purine nucleosidesCHEMONTID:0003727Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group and at the 2-position with either a purine base.
Phosphonated cyclopropyl pyrimidine nucleosidesCHEMONTID:0003728Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group and at the 2-position with either a pyrimidine base.
1,2-substituted phosphonated cyclopentyl nucleosidesCHEMONTID:0003742Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 2-position with either a purine or pyrimidine base.
1,3-substituted phosphonated cyclopentyl nucleosidesCHEMONTID:0003743Nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 3-position with either a purine or pyrimidine base.
Cedrane and isocedrane sesquiterpenoidsCHEMONTID:0003752Sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position.
Kaurane diterpenoidsCHEMONTID:0003782Diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.
Aconitane-type diterpenoid alkaloidsCHEMONTID:0003788Alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.
Lappaconitine-type diterpenoid alkaloidsCHEMONTID:0003789C18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position.
Ranaconitine-type diterpenoid alkaloidsCHEMONTID:0003790C18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lycoctonine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position.
(3'->5')-cyclic dinucleotide bis(phosphoromonothioate) analoguesCHEMONTID:0003793Cyclic compounds consisting of two ribose moieties connected two 5',3'-phosphomonothioic acid O,O'-diester bonds to form a cycle. Each ribose unit is N-linked to a nucleic base or an analogue thereof.
(3'->5')-cyclic dinucleotide phosphoromonothioate analoguesCHEMONTID:0003794Cyclic compounds consisting of two ribose moieties connected one 5',3'-phosphomonothioic acid O,O'-diester bond and one phosphodiester bond, to form a cycle. Each ribose unit is N-linked to a nucleic base or an analogue thereof.
(3'->5')-cyclic dinucleotide phosphorotrithioate analoguesCHEMONTID:0003795Cyclic compounds consisting of two ribose moieties connected one 5',3'-phosphomonothioic acid O,O'-diester bond and one 5',3'-phosphodithioic acid O,O'-diester to form a cycle. Each ribose unit is N-linked to a nucleic base or an analogue thereof.
Mono-(1Z-alkenyl)-glycerolsCHEMONTID:0003806Monoradylglycerolipids that carry exactly one 1Z-alkyenyl chain attached to the glycerol moiety.
DialkylglycerolsCHEMONTID:0003810Glycerides consisting of two fatty acid chains covalently bonded to a glycerol molecule through ether linkages.
1-alkyl,3-acylglycerolsCHEMONTID:0003811Glycerides consisting of two fatty acyl chains covalently bonded to a glycerol molecule at the 1- and 3-positions through an ether and an ester linkage, respectively.
1-acyl,2-alkylglycerolsCHEMONTID:0003812Glycerides consisting of two fatty acyl chains covalently bonded to a glycerol molecule at the 2- and 1-positions through an ether and an ester linkage, respectively.
1-alkyl,2-acylglycerolsCHEMONTID:0003813Glycerides consisting of two fatty acyl chains covalently bonded to a glycerol molecule at the 1- and 2-positions through an ether and an ester linkage, respectively.
AlkyldiacylglycerolsCHEMONTID:0003814Triradylglycerols that carry exactly two acyl chains attached to the glycerol moiety through an ester linkage, and one attached through an ester linkage.
1Z-alkenyldiacylglycerolsCHEMONTID:0003816Triradylglycerols that carry exactly two acyl chains attached to the glycerol moiety through an ester linkage, a 1-Z-alkenyl chain and attached through an ether linkage.
DialkylmonoacylglycerolsCHEMONTID:0003817Triradylglycerols that carry exactly two acyl chains attached to the glycerol moiety through an ether linkage, and one 1Z-alkenyl chain attached through an ester linkage.
1Z-alkenylacylglycerolsCHEMONTID:0003824Diradylglycerols that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage, and one 1Z-alkenyl chain attached through an ether linkage.
1-acyl,2-(1Z-alkenyl)-glycerophosphocholinesCHEMONTID:0003826Glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O1-position, and one 1Z-alkenyl chain attached through an ether linkage at the O2-position.
1-(1Z-alkenyl),2-acyl-glycerophosphocholinesCHEMONTID:0003827Glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
1-acyl,2-alkylglycero-3-phosphocholinesCHEMONTID:0003828Glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O1-position, and one acyl chain attached through an ether linkage at the O2-position.
1-alkyl,2-acylglycero-3-phosphocholinesCHEMONTID:0003829Glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one alkyl chain attached through an ether linkage at the O1-position.
1-alkyl,2-acylglycerophosphoethanolaminesCHEMONTID:0003830Glycerophosphoethanolamines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one alkyl chain attached through an ether linkage at the O1-position.
DialkylglycerophosphoethanolaminesCHEMONTID:0003831Glycerophosphoglycerols that carry exactly two chains attached to the glycerol moiety through ether linkages.
1-(1Z-alkenyl),2-acylglycerophosphoethanolaminesCHEMONTID:0003832Glycerophosphoethanolamines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
MonoalkylglycerophosphoethanolaminesCHEMONTID:0003833Glycerophosphoethanolamines that carry exactly one alkyl chain attached to the glycerol moiety through a ether linkage.
1-(1Z-alkenyl)-glycero-3-phosphoethanolaminesCHEMONTID:0003834Glycerophosphoglycerophosphates that carry exactly one 1Z-alkenyl chain attached to the glycerol moiety through an ether linkage.
DialkylglycerophosphoserinesCHEMONTID:0003836Glycerophosphoserines that contain exactly two fatty acyl chains attached to the glycerol moiety through ether linkages.
Monoalkylglycerol-3-phosphoserinesCHEMONTID:0003837Lipids containing a glycerol moiety carrying a phosphoserine at the 3-position, as well as an alkyl chain attached to the glycerol moiety through an ether linkage.
1Z-alkenylglycero-3-phosphoserinesCHEMONTID:0003838Glycerophosphocholines that carry exactly one 1Z-alkenyl chain attached to the glycerol moiety through an ether linkage.
1-alkyl,2-acylglycerophosphoglycerolsCHEMONTID:0003839Glycerophosphoglycerols that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one alkyl chain attached through an ether linkage at the O1-position.
1-(1Z-alkenyl),2-acylglycerophosphoglycerolsCHEMONTID:0003840Glycerophosphoglycerols that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
DialkylglycerolphosphoglycerolsCHEMONTID:0003841Glycerophosphoglycerols that carry exactly two alkyl chain attached to the glycerol moiety through ether linkages.
MonoalkylglycerophosphoglycerolsCHEMONTID:0003842Glycerophosphoglycerols that carry exactly one alkyl chain attached to the glycerol moiety through an ether linkage.
1-(1Z-alkenyl)glycerophosphoglycerolsCHEMONTID:0003843Glycerophosphoglycerols that carry exactly one 1Z-alkenyl chain attached to the glycerol moiety through an ether linkage.
MonoacylglycerophosphomonoradylglycerolsCHEMONTID:0003844Glycerophosphomonoradylglycerols that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage.
DiacylglycerophosphomonoradylglycerolsCHEMONTID:0003845Glycerophosphomonoradylglycerols that carry exactly two acyl chains attached to the glycerol moiety through ester linkages.
1-alkyl,2-acylglycerophosphoglycerophosphatesCHEMONTID:0003846Glycerophosphoglycerophosphates that contain exactly two fatty acyl chains attached to the glycerol moiety, one through an ester linkage at the O2-position, and the other through an ether linkage at the O1-position.
1-(1Z-alkenyl),2-acylglycerophosphoglycerophosphatesCHEMONTID:0003847Glycerophosphoglycerophosphates that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
1-alkyl,2-acylglycerophosphoinositolsCHEMONTID:0003848Glycerophosphoinositols that contain exactly two fatty acyl chains attached to the glycerol moiety, one through an ester linkage at the O2-position, and the other through an ether linkage at the O1-position.
1-(1Z-alkenyl),2-acylglycerophosphoinositolsCHEMONTID:0003849Glycerophosphoinositols that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
DialkylglycerophosphoinositolsCHEMONTID:0003850Glycerophosphoinositols that contain exactly two fatty acyl chains attached to the glycerol moiety, one through ether linkages at the O1- and O2-positions.
MonoalkylglycerophosphoinositolsCHEMONTID:0003851Glycerophosphoinositols that contain exactly on fatty acyl chain attached to the glycerol moiety through an ether linkage.
1-(1Z-alkenyl)glycerophosphoinositolsCHEMONTID:0003852Glycerophosphoinositols that carry exactly one 1Z-alkenyl chain attached to the glycerol moiety through an ether linkage.
DolicholsCHEMONTID:0003854A group of long-chain mostly unsaturated organic compounds that are made up of varying numbers of isoprene units terminating in an alpha-saturated isoprenoid group, containing an alcohol functional group. The three isoprene units at the distal end are trans-linked.
BactoprenolsCHEMONTID:0003858Compounds consisting of a (un-) substituted bactoprenyl group, which is a C-55 isoprenoid alcohol obtained by condensation of 10 unsaturated isoprene units a one saturated isoprene unit.
Fatty acyl glycosides of mono- and disaccharidesCHEMONTID:0003861Compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
AlkylarylthioethersCHEMONTID:0003863Organosulfur compounds containing a thioether group that is substituted by an alkyl and an aryl group.
DiarylthioethersCHEMONTID:0003864Organosulfur compounds containing a thioether group that is substituted by two aryl groups.
Phosphoric diester monoamidesCHEMONTID:0003869Organophosphorus compounds containing a monoamide derivative of a phosphoric acid diester functional group. They have the general structure R1OP(=O)(OR2)N(R3)R4, where R1-R2 = organyl group and R3-R4 = H or organyl.
Organic phosphoric acid triamidesCHEMONTID:0003871Organophosphorus compounds with the general formula RNP(R2)(R3)=O (R=alkyl, aryl; R2-R3 = amine groups).
Oxime estersCHEMONTID:0003879Organic compounds containing an ester derivative of the oxime functional group.
Hydroxamic acid estersCHEMONTID:0003880Hydroxamic acids in which the hydrogen of the hydroxy group has been replaced by an organyl group.
Cyclic carboximidic acidsCHEMONTID:0003881Organic acids with the general formula RC(=N)-OH (R=H, organic group), where the carboximidic acid group is part of a cycle.
ImidolactonesCHEMONTID:0003882Cyclic organooxygen compounds with the general structure R(=N)OR' where the central carbon atom is part of a ring, and R,R' = organyl group.
Cyclic imidothioic acidsCHEMONTID:0003884Organic compounds containing the imidothioic acid group as part of a cycle.
Ketene silyl acetalsCHEMONTID:0003895Organosilicon compounds with the general structure OC(O[Si])=CR, where R = H or organyl group.
Silyl monohalidesCHEMONTID:0003896Organosilicon compounds with the general formula RSi(R')(R'')X; R-R'' = organyl group, X = halogen atom.
Silyl dihalidesCHEMONTID:0003897Organosilicon compounds with the general formula RSi(R')(X)X; R-R' = organyl group, X = halogen atom.
Silyl trihalidesCHEMONTID:0003898Organosilicon compounds with the general formula RSi(X)(X)X; R = organyl group, X = halogen atom.
AralkylaminesCHEMONTID:0003899Alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
N-acetoxyarylaminesCHEMONTID:0003900Arylamines that contain an acetytoxy group attached to the nitrogen.
5-amino-2-aroylquinolinesCHEMONTID:0003911Compounds containing a quinoline which carries an aroyl group at the 2-position, and an amino group at the 5-position.
Organic potassium saltsCHEMONTID:0003927Organic compounds containing a potassium ion.
Organic sodium saltsCHEMONTID:0003928Organic compounds containing a sodium ion.
Dialkyl peroxidesCHEMONTID:0003951Organic compounds containing a peroxide group substituted by two alkyl groups.
2-aminoanthraquinonesCHEMONTID:0003952Organic compounds containing an anthraquinone ring system, which is substituted at the 2-position by an amino group.
BenzidinesCHEMONTID:0003955Organic compounds containing the benzidine skeleton, made up of a biphenyl ring system substituted at the 4- and 4'-positions with a unsubstituted amine group.
Perfluoroalkyl carboxylic acid and derivativesCHEMONTID:0003962Organic compounds containing an alkyl chain attached to the C-alpha of a carboxylic acid group (or a derivative thereof), where all hydrogens of the alkyl chain are replaced by fluorine atoms.
Perfluoroalkyl phosphonic acid and derivativesCHEMONTID:0003963Organic compounds containing an alkyl chain attached to the phosphorus of a phosphonic acid group (or a derivative thereof), where all hydrogens of the alkyl chain are replaced by fluorine atoms.
Perfluoroalkyl sulfonic acid and derivativesCHEMONTID:0003961Organic compounds containing an alkyl chain attached to the sulfur of a sulfonic acid group (or a derivative thereof), where all hydrogens of the alkyl chain are replaced by fluorine atoms.
AminotoluenesCHEMONTID:0003964Organic aromatic compounds containing a benzene that carries a single methyl group and one amino group.
Fluorotelomer alcoholsCHEMONTID:0003967Fluorocarbon-based oligomers linked to an alcohol chain.
DinitroanilinesCHEMONTID:0003968Organic compounds containing an aniline moiety, which is substituted at 2 positions by a nitro group.
NitrotoluenesCHEMONTID:0004108Organic aromatic compounds containing a benzene that carries a single methyl group and at least 1 nitro group.
PolyhalopyridinesCHEMONTID:0003971Organic compounds containing a pyridine ring substituted at two or more positions by a halogen atom.
CarbonylnitrenesCHEMONTID:0003974Organic compounds containing a nitrene to which a carbonyl group is attached.
SulfonylnitrenesCHEMONTID:0003975Organic compounds containing a nitrene to which a sulfonyl group is attached.
Alkyldimethylbenzylammonium chloridesCHEMONTID:0003977Organic compounds consisting of a quaternary ammonium group substituted with a benzyl group, two methyl groups as well as an alkyl chain. These compounds also contain a chlorine ion and have the general structure R1[N+](CH3)(CH3)R2.[Cl-], where R1 = benzyl group and R2 = alkyl chain.
Benzyl bromidesCHEMONTID:0003979Organic compounds containing a benzene skeleton substituted with a bromomethyl group.
Benzyl chloridesCHEMONTID:0003980Organic compounds containing a benzene skeleton substituted with a chloromethyl group.
Benzyl fluoridesCHEMONTID:0003982Organic compounds containing a benzene skeleton substituted with a fluoromethyl group.
Toluene diisocyanatesCHEMONTID:0003983Organic compounds containing a benzene ring, which is substituted by a methyl group and two isocyanate groups.
ArsinesCHEMONTID:0003984AsH3 and compounds derived from it by substituting one, two or three hydrogen atoms by hydrocarbyl groups: R3As, RAsH2, R2AsH, R3As (R is not H) are called primary, secondary and tertiary arsines, respectively.
Oxygen-containing organoarsenic compoundsCHEMONTID:0004280Organoarsenic compounds that containing an oxygen atom.
Arsine imidesCHEMONTID:0003987Hydrocarbyl derivatives of H3As=N.
Arsine sulfidesCHEMONTID:0003988Hydrocarbyl derivatives of H3As=S.
Organosulfonic anhydridesCHEMONTID:0003990Organic compounds having the structure RS(=O)2OS(=O)2R', where R = organyl group and R' = H or organyl group.
Organic cobalt saltsCHEMONTID:0003995Organic salt compounds containing a cobalt atom in its ionic form.
MethoxyanilinesCHEMONTID:0003999Organic compound containing an aniline group substituted at one or more positions by a methoxy group.
2-aminothiophenesCHEMONTID:0004004Organic compounds containing an amino group conjugated to a thiophene ring at the 2-position.
ChloroquinolinesCHEMONTID:0004008Compounds containing a quinoline moiety, which carries one or more chlorine atoms.
Organic copper saltsCHEMONTID:0004018Organic salt compounds containing a copper atom in its ionic form.
Alkyl lead compoundsCHEMONTID:0004027Organolead compounds containing one or more alkyl chains attached to the lead atom.
Organic tin saltsCHEMONTID:0004038Organic salt compounds containing a tin atom in its ionic form.
Organic aluminium saltsCHEMONTID:0004041Organic salt compounds containing a tin atom in its ionic form.
Alkyl mercury compoundsCHEMONTID:0004042Organometallic compounds containing an alkyl group attached to a mercury atom.
Aryl mercury compoundsCHEMONTID:0004043Organometallic compounds containing an aryl group attached to a mercury atom.
Perfluoroalkanesulfonyl fluoridesCHEMONTID:0004050Organic compounds containing an alkyl chain attached to the sulfur of an organosulfonyl fluoride group, where all hydrogens of the alkyl chain are replaced by fluorine atoms.
Organic lead saltsCHEMONTID:0004051Organic salts containing a lead ion.
Trivalent organic arsenic compoundsCHEMONTID:0004055Organoarsenic compounds in which a carbon is linked to a trivalent arsenic atom.
Pentavalent organic arsenic compoundsCHEMONTID:0004056Organoarsenic compounds in which a carbon is linked to a pentavalent arsenic atom.
Organic silver saltsCHEMONTID:0004063Organic salt compounds containing a copper atom either in its ionic form or bonded to another atom.
Transition metal cyanide saltsCHEMONTID:0004064Organic compounds containing a transition metal and a cyanide ion [C-]#N.
Triorganolead compoundsCHEMONTID:0004065Compounds containing a lead compound bonded to three carbon atoms.
Triorganotin compoundsCHEMONTID:0004066Compounds containing a tin compound bonded to exactly three carbon atoms.
TrialkylstibanesCHEMONTID:0004069Organoantimony compounds containing a trivalent antimony atom linked to exactly three alkyl chains.
MonoalkyltinsCHEMONTID:0004070Triorganotin compounds where the tin atom is linked to exactly one alkyl groups.
DialkyltinsCHEMONTID:0004071Triorganotin compounds where the tin atom is linked to exactly two alkyl groups.
Organic cadmium saltsCHEMONTID:0004075Organic salts of cadmium. They usually contain cadmium in its ionic form.
Organic antimony saltsCHEMONTID:0004078Organic salts of antimony. They usually contain antimony in its ionic form.
N-vinylaziridinesCHEMONTID:0004080Compounds containing an aziridine ring where the nitrogen atom is substituted by a vinyl group.
Iridoid O-glycosidesCHEMONTID:0004081Iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.
Acyl nitratesCHEMONTID:0004087Organic compounds containing a nitrate that is O-linked to an acyl group.
Peroxyacyl nitratesCHEMONTID:0004088Organic compounds containing a peroxide group linked to an acyl group and a nitrate group.
Alkyl nitratesCHEMONTID:0004091Organic compounds containing a nitrate that is O-linked to an alkyl group.
Acyl nitritesCHEMONTID:0004092Organic compounds containing an acyl group linked to a nitrite group.
Alkyl nitritesCHEMONTID:0004093Organic compounds containing an alkyl group linked to a nitrite group.
Alkyl perchloratesCHEMONTID:0004094Organic compounds containing perchlorate group attached to an alkyl group.
Imidazo[1,5-a][1,4]benzodiazepinesCHEMONTID:0004098Compounds containing an imidazole ring and a 1,4-benzodiazepine ring system, both sharing one nitrogen atom.
1-benzoylpiperidinesCHEMONTID:0004110Compounds containing a piperidine ring substituted at the 1-position with a benzoyl group.
DimethoxybenzenesCHEMONTID:0004111Organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups.
Alpha-imino acidsCHEMONTID:0004114Organic acids containing an imino group attached to a carbon, which in turn is immediately linked to a carboxyl group. They have the generic structure RN=CC(=O)OH or RN=CC(=O)[O-] (salt form), where R is any atom.
C-nitro compoundsCHEMONTID:0004117Compounds having the nitro group, -NO2 (free valence on nitrogen), which is attached to carbon.
Alpha-imino acid estersCHEMONTID:0004133Ester derivatives of alpha-imino acids. They have the general structure RN=CC(=O)OR', where R = H, organyl group and R' = organyl group.
S-alkyl-thiohydroximatesCHEMONTID:0004138Organosulfur compounds with the general structure RC(S)=NOH, where R =alkyl group.
PhenylpyridazinesCHEMONTID:0004147Organic compounds containing a pyridazine ring substituted by a phenyl group.
Cladiellane diterpenoidsCHEMONTID:0004153Diterpenoids containing a cladiellane skeleton. Cladiellane is a tricyclic ring system derived from eunicellane.
Steroidal alkaloid glycosidesCHEMONTID:0004156Compounds made up of a steroidal alkaloid moiety which is glycosylated, usually at the C-3 or C-28 position.
1-hydroxysteroidsCHEMONTID:0004158Steroids carrying a hydroxyl group at the 1-position of the steroid backbone.
18-hydroxysteroidsCHEMONTID:0004159Steroids carrying a hydroxyl group at the 18-position of the steroid backbone.
TrihalomethanesCHEMONTID:0004160Organic compounds in which exactly three of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
HydroxypyrimidinesCHEMONTID:0004161Organic compounds containing a hydroxyl group attached to a pyrimidine ring. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
ThiopyrimidinesCHEMONTID:0004173Aromatic heterocyclic compounds containing a pyrimidine ring that has one or more carbon atoms involved in a C=S bond.
S-alkylsulfenatesCHEMONTID:0004175Organosulfur compounds containing a sulfenic acid, where the sulfur atom is linked to an alkyl group. They have the general formula RSOH, where R is an alkyl group.
Ethylene bisdithiocarbamatesCHEMONTID:0004177Dithiocarbamic acids (or derivatives) resulting from the formal addition of a molecule of carbon disulfide to each amino group of ethylenediamine. In addition, compounds containing a 1,2-ethanediyl carbamodithioate moiety are also members of this class.
1-(1Z-alkenyl),3-acylglycerophosphoethanolaminesCHEMONTID:0004178Glycerophosphoethanolamines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O3-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
3-sulfated flavonoidsCHEMONTID:0004181Flavonoids that are sulfated at the 3-ring position of the flavonoid skeleton.
Long-chain alkyl amine oxidesCHEMONTID:0004183Aminoxides that carry an alkyl chain ranging from C10 to C24.
Trialkyl amine oxidesCHEMONTID:0004184Hydrocarbyl derivatives of the aminoxide anion, with the general formula R3N+[O-] or R3N=O, where R is an alkyl group.
3-alkylindolesCHEMONTID:0004196Compounds containing an indole moiety that carries an alkyl chain at the 3-position.
1,3,5-dithiazinanesCHEMONTID:0004199Cyclic compounds that contain a dithiazinane ring, which is a saturated heterocycle that consisting of one nitrogen atom, two sulfur atoms at the 1-,3-, and 5- position, respectively.
HydroxyanilidesCHEMONTID:0004200Compounds that contain an anilide moiety, where the benzene ring carries a hydroxyl group.
1-sulfamoyl-1,2,3-triazolesCHEMONTID:0004202Compounds containing a 1,2,3-triazole that carries a sulfamoyl group at the 1-position.
PhenylbenzaminesCHEMONTID:0004204Aromatic compounds consisting of a benzyl group that is N-linked to a benzamine.
FurancarboxamidesCHEMONTID:0004205Compounds containing a furan ring that carries a carboxamide group.
m-XylenesCHEMONTID:0004209Aromatic compounds that contain a m-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 3-positions.
o-XylenesCHEMONTID:0004210Aromatic compounds that contain a o-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 2-positions.
p-XylenesCHEMONTID:0004211Aromatic compounds that contain a p-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 4-positions.
XylenolsCHEMONTID:0004212Aromatic compounds that contain a xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups, and at least one hydroxyl group.
AnilinopyrimidinesCHEMONTID:0004216Aromatic heterocyclic compounds containing an anilinopyrimidine skeleton, which consists of an aniline that is N-substituted by a pyrimidine.
AllylaminesCHEMONTID:0004218Organic compound containing an allyl group and an amine group, with the general structure R2C=C(H)N(R'2), where R-R'=H or organyl.
ToluamidesCHEMONTID:0004219Aromatic compounds containing a toluene, which carries a carboxamide group.
Tetraalkylammonium saltsCHEMONTID:0004225Organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
1,2,4-triazolo[4,3-a][1,4]benzodiazepinesCHEMONTID:0004226Aromatic compounds containing a 1,4-benzodiazepine fused to and sharing a nitrogen atom with a 1,2,4-triazole ring.
1-(1Z-alkenyl),3-acyl-glycerophosphatesCHEMONTID:0004227Glycerophosphates that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O3-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
1-(1Z-alkenyl),3-acyl-glycerol-2-phosphocholinesCHEMONTID:0004228Glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O3-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
Pyrrolo[2,1-c][1,4]benzodiazepinesCHEMONTID:0004230Heterocyclic aromatic compounds containing a 1,4-benzodiazepine ring system that is fused to, and shared a nitrogen atom with a pyrrole ring.
Benzenesulfonyl halidesCHEMONTID:0004308Aromatic compounds containing a benzenesulfonyl group, where the sulfonyl moiety is singly boned to an halogen atom.
Azetidino[1,2-d][1,4]benzodiazepinesCHEMONTID:0004235Aromatic heterocyclic compounds containing a 1,4-benzodiazepine ring system fused to and sharing a nitrogen atom with an azetidine.
Tetraorganoarsonium saltsCHEMONTID:0004238Organoarsenic compounds, where the arsenic atom is tetrasubstituted by organic groups. They have the general structure R4[As+]X-, X=any atom but H.
Sulfur-containing organoarsenic compoundsCHEMONTID:0004240Organoarsenic compounds that containing a sulfur atom.
OrganotetrahaloarsoranesCHEMONTID:0004243Organoarsenic compounds, having a pentavalent arsenic atom linked to four halogen atoms and a organic group.
Tetraorganostibonium saltsCHEMONTID:0004249Organoantimony compounds containing an antimony cation that is tetrasubstituted with four organic groups, and which interacts with an anion.
Pyridoxamine 5'-phosphatesCHEMONTID:0004259Heterocyclic aromatic compounds containing a pyridoxamine that carries a phosphate group at the 5'-position.
3-Acylpyruvic acidsCHEMONTID:0004268Compounds containing a pyruvic acid substituted at the 3-position by an acyl group.
MonohaloarsinesCHEMONTID:0004281Organoarsenic compounds with the general formula R[As](R')X, where R = Organyl group, R'=H atom or Organyl group, and X = halogen atom.
DihaloarsinesCHEMONTID:0004282Organoarsenic compounds with the general formula R[As](X)X, where R = Organyl group, and X = halogen atom.
Organotin selenidesCHEMONTID:0004285Organotin compounds containing a divalent selenium atom linked to two tin atoms, each linked to at least one organyl group.
Organotin sulfidesCHEMONTID:0004286Organotin compounds containing a divalent sulfur atom linked to two tin atoms, each linked to at least one organyl group.
Organotin telluridesCHEMONTID:0004287Organotin compounds containing a divalent tellurium atom linked to two tin atoms, each linked to at least one organyl group.
Organolead sulfidesCHEMONTID:0004288Organolead compounds containing a divalent selenium atom linked to two lead atoms, each linked to at least one organyl group.
Tetraorganolead compoundsCHEMONTID:0004289Compounds containing a lead compound bonded to four carbon atoms.
Primary stibinesCHEMONTID:0004290Organoantimony hydrides in which the antimony tom is bond to one carbon atom and two hydrogen atoms. They have the generic structure RAsH2.
Secondary stibinesCHEMONTID:0004291Organoantimony hydrides in which the antimony tom is bond to two carbon atoms and an hydrogen atom. They have the generic structure R2AsH.
1,2,4-benzothiadiazine-1,1-dioxidesCHEMONTID:0004292Aromatic heterocyclic compounds containing a 1,2,4-benzothiadiazine ring system with two S=O bonds at the 1-position.
4-HydrocarbylideneazlactonesCHEMONTID:0004303Heterocyclic compounds containing a substituted 1,3-oxazoline ring, and with the general structure RC(R')=C1N=C(R'')OC1=O. They are often referred to as 'unsaturated azlactones'.
Benzenesulfonate estersCHEMONTID:0004309Arenesulfonate esters that result from the formal condensation of the hydroxy group of an alcohol, enol, phenol or heteroarenol with benzenesulfonic acid.
2-nitrothiophenesCHEMONTID:0004337Aromatic heterocyclic compound containing a nitro group attached to a thiophene ring a the 2-position.
3-nitrothiophenesCHEMONTID:0004338Aromatic heterocyclic compound containing a nitro group attached to a thiophene ring a the 3-position.
NitrohalothiophenesCHEMONTID:0004339Aromatic heterocyclic compound containing a thiophene ring that carries a nitro group, as well as an halogen atom.
Phenyl-1,3-oxazolesCHEMONTID:0004342Aromatic heterocyclic compounds containing a 1,3-oxazole substituted at one or more positions by a phenyl group.
Tetraorganotin compoundsCHEMONTID:0004348Compounds containing a tin compound bonded to exactly four carbon atoms.
(3'->5')-cyclic dinucleotide bis(carbamate) analoguesCHEMONTID:0004352(3'->5')-cyclic dinucleotides in which the two phosphodiester bonds are replaced by two isosteric carbamate linkages.
Benzenecarbothioic S-acidsCHEMONTID:0004355Aromatic compounds containing a benzene ring that carries a carbothioic S-acid group.
Acylaminobenzoic acid and derivativesCHEMONTID:0004361Derivatives of amino benzoic acid derivatives where the amine group is N-acylated.
Organic chromium saltsCHEMONTID:0004369Organic salt compounds containing a chromium atom in its ionic form.
5-Benzylpyrimidine-2,4-diaminesCHEMONTID:0004386Aromatic heterocyclic compounds containing a 2,4-diaminopyrimidine moiety that is substituted at the 5-position by a benzyl group.
2'-AminoanilidesCHEMONTID:0004389Organic compounds containing an anilide moieties that carries an amino group at the 2-position of the benzene ring.
4-AnilinoquinazolinesCHEMONTID:0004391Organic heterocyclic compounds containing a quinazoline that is N-linked to an aniline.
6-Amino-4-phenyltetrahydroquinolinesCHEMONTID:0004393Aromatic heterocyclic compounds containing a tetrahydroquinoline ring system substituted at the 4- and the 6- positions with a phenyl group and an amine group, respectively.
3-arylsulfonyl-pyrazolo[1,5-a]pyrimidinesCHEMONTID:0004406Aromatic heteropolycyclic compounds that contain a pyrazolo[1,5-a]pyrimidine ring system, which is substituted at the 3-position by an arylsulfonyl group.
BenzoylpyrazolesCHEMONTID:0004704Aromatic compounds containing a benzoyl group substituted with a pyrazole ring.
2-amino-pyrido[2,3-d]pyrimidinesCHEMONTID:0004420Compounds containing the pyrido[2,3-d]pyrimidine ring system, which carries an amine at the 2-position. Pyrido[2,3-d]pyrimidine is a pyridopyrimidine isomer with three ring nitrogen atoms at the 1-, 3-, and 8- position.
Benzo[f]quinolin-3-onesCHEMONTID:0004423Aromatic organonitrogen heterocyclic compounds that contain a benzo[f]quinoline ring system carrying an oxo group at the 3-position.
Pyrrolo[3,2-c]quinolinesCHEMONTID:0004424Aromatic organonitrogen heterocyclic compounds containing a pyrrolo[3,2-c]quinoline, a pyrroloquinoline isomer that posseses two ring nitrogen atoms at the 1- and 5-positions.
Thiocarbamate saltsCHEMONTID:0004428Salts of thiocarbamic acids.
AlkylchloroformatesCHEMONTID:0004431Compounds containing a chloroformic acid group that is esterified with an alkyl group.
OrganoheterosilanesCHEMONTID:0004445Organosilicon compounds where the tetravalent silicon atom is linked to one or more heteroatoms.
Metal carbonate saltsCHEMONTID:0004449Organic salts that results from the interaction of a metal ion with a negatively charged oxygen atom of the carbonate ion.
Acrylic acidsCHEMONTID:0004451Organic compounds containing acrylic acid CH2=CHCO2H.
Acrylic acid estersCHEMONTID:0004452Organic compounds containing and ester acrylic acid (CH2=CHC(=O)OH).
Alkyl azidesCHEMONTID:0004465Compounds bearing the group N3, viz. -N=N+=N- attached to an alkyl group.
Aryl azidesCHEMONTID:0004466Compounds bearing the group N3, viz. -N=N+=N- attached to an aryl group.
Alkenyl azidesCHEMONTID:0004473Compounds bearing the group N3, viz. -N=N+=N- attached to an alkenyl group.
Trimethylsilyl estersCHEMONTID:0004481Organoheterosilanes, bearing a silicon atom that is linked to three methyl groups and is O-esterified.
Dialkyl alkylphosphonatesCHEMONTID:0004482Compounds containing a phosphonic acid that is diesterified with alkyl groups, and the phosphorus atom is also directly attached to an alkyl group.
O-alkylpyrimidinesCHEMONTID:0004486Compounds containing a pyrimidine , which is O-alkylated at one or more ring positions.
Organic lithium saltsCHEMONTID:0004488Organic compounds containing a lithium ion.
14-hydroxysteroidsCHEMONTID:0004495Steroids carrying a hydroxyl group at the 14-position of the steroid backbone.
DinitrophenolsCHEMONTID:0004505Organic aromatic compounds containing a benzene that carries a single phenol group and exactly two nitro groups.
N-acetylarylaminesCHEMONTID:0004506Acetamides where one or more amide hydrogens is substituted by an aryl group.
1,2,3-thiadiazolopyridinesCHEMONTID:0004509Aromatic heterocyclic compounds containing a pyridine fused to a 1,2,3-thiadiazole ring.
AlkylhydrazinesCHEMONTID:0004511Organonitrogen compounds that containing a hydrazine group to which an alkyl group is attached.
N-sulfenyl-N'-sulfonyl-ureasCHEMONTID:0004514Urea derivatives that carry a sulfonyl group at one nitrogen atom of the urea backbone, and a sulfenyl group at the other nitrogen atom.
Brominated dibenzofuransCHEMONTID:0004520Organic compounds containing a bromine atom attached to a dibenzofuran moiety.
ChlorofluorocarbonsCHEMONTID:0004521Alkyhalide compounds that are composed only of chlorine, fluorine, and carbon atoms.
HydrofluorocarbonsCHEMONTID:0004522Alkyhalide compounds that are composed only of hydrogen, fluorine, and carbon atoms.
ChlorophenoxyacetatesCHEMONTID:0004525Compounds containing a phenoxyacetate that carries one or more chlorine atoms on the benzene ring.
ChloroanilinesCHEMONTID:0004526Aromatic compounds containing an aniline moiety substituted at one or more positions with a chlorine atom.
HalotoluenesCHEMONTID:0004528Aromatic compounds containing a toluene that is substituted at one or more ring positions with a halogen atom.
2-halopyridinesCHEMONTID:0004532Organic compounds containing a pyridine ring substituted at the 2-position by a halogen atom.
4-aminoquinolinesCHEMONTID:0004537Organic compounds containing an amino group attached to the 4-position of a quinoline ring system.
HalonitrobenzenesCHEMONTID:0004541Compounds containing a nitrobenzene moiety, where the benzene ring carries an halogen atom.
N-methylpyridinium compoundsCHEMONTID:0004543Methylpyridines that carry a methyl group at the 1-position.
Indazole-3-carboxamidesCHEMONTID:0004552Aromatic compounds containing an indazole ring system that is substituted at the 3-position with a carboxamide group.
NitriminesCHEMONTID:0004554Compounds having the structure O2NN=CR2 (also called N-nitroimines).
Cyanate estersCHEMONTID:0004560Esters of cyanic acid, with the general formula R-OC#N (R = organyl group).
N-cinnamoylanthranilic acidsCHEMONTID:0004561Aromatic compounds containing a cinnamic acid conjugated to an anthranilic acid.
Metal cyanatesCHEMONTID:0004562Compounds containing a metal atom and a cyanate. The metal cyanate group can be in neutral or ionic form (involving a cationic metal and the anionic cyanate).
Ethoxyethynyl alcoholsCHEMONTID:0004564Organic compounds containing an ethoxyethynyl group substituted with an alcohol group.
Alkylaluminium and derivativesCHEMONTID:0004568Organoaluminium compounds where the aluminium atom is linked to an alkyl group.
AlkylboranesCHEMONTID:0004570Organoboron compounds where the boron atom is substituted by one or more alkyl groups.
Diacyl peroxidesCHEMONTID:0004579Organooxygen compounds containing a peroxide disubstituted with acyl groups.
Trialkylantimony halidesCHEMONTID:0004583Organoantimony compounds where the tetravalent or pentavalent antimony atom is substituted by an halogen atom and exactly three alkyl groups.
ArenediazoatesCHEMONTID:0004587Diazoethers which are N-substituted with an aryl group through a CN bond.
DialkylzincsCHEMONTID:0004593Organozinc compounds containing a zinc atom that is disubstituted with alkyl groups. They have the general formula RZnR', where R and R' are alkyl groups.
Organomagnesium halidesCHEMONTID:0004594Organomagnesium compounds with the formula RMgX, where R=organyl group, and X = halogen atom.
DialkylmagnesiumsCHEMONTID:0004597Organomagnesium compounds where the magnesium atom is substituted with two alkyl groups. They have the general formula RMgR', where R and R' are alkyl groups.
Aromatic 3-cyanotriazenesCHEMONTID:0004600Organonitrogen compounds containing a 3-cyanotriazene moiety which is substituted at the terminal amine with an aromatic group.
Diazonium perchloratesCHEMONTID:0004602Organic perchlorate compounds with the general structure RN+2 ClO4-, where R is an organyl group.
Diazonium tetrahaloboratesCHEMONTID:0004605Organic compounds containing a tetrahaloborate ion and a diazonium ion.
1,1-dinitrodifluoraminesCHEMONTID:0004608Difluoroamino compounds contaning two nitro groups and with the general structure RC(NO2)2NF2.
Metal p-nitrophenoxidesCHEMONTID:0004610Para-nitrophenoxide derivatives that are linked to a metal atom.
NitrobenzaldehydesCHEMONTID:0004613Nitrobenzenes that carry an aldehyde group at any position of the benzene ring.
Aryl phosphatesCHEMONTID:0004616Organophosphorus compounds having a phosphate group substituted by one or more aryl groups.
Branched alkanesCHEMONTID:0004620Acyclic branched hydrocarbons having the general formula CnH2n+2.
Branched cycloalkanesCHEMONTID:0004621Acyclic unbranched hydrocarbons having the general formula CnH2n+2.
Aryl thiophosphatesCHEMONTID:0004623Organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where at least one R-group is an aryl group.
Benzyl alkyl sulfoxidesCHEMONTID:0004630Organosulfur compounds that contain a sulfoxide group substituted by a benzyl group, and an alkyl group. They have the general structure RS(=O)R' ( R=benzyl, R'=alkyl).
1,2-allenyl phenyl sulfoxidesCHEMONTID:0004633Organosulfur compounds containing a sulfoxide group substituted with a phenyl group and a 1,2-allenyl group.
Phenyl sulfidesCHEMONTID:0004634Organosulfur compounds containing a thioether group that is substituted by a phenyl group.
Dibenzothiophene-5-oxidesCHEMONTID:0004635Organic aromatic compounds containing a dibenzothiophene disubstituted at the 5-position with a dioxide group.
Dibenzothiophene-5,5-dioxidesCHEMONTID:0004636Organic aromatic compounds containing a dibenzothiophene disubstituted at the 5-position with two dioxide groups.
Alkyl-2-thio-S-triazinesCHEMONTID:0004637Aromatic compounds containing a 1,3,5-triazine ring that is substituted at the 2-position with a S-alkyl group.
Alkoxy-S-triazinesCHEMONTID:0004638Aromatic compounds containing a 1,3,5-triazine ring that is substituted at the 2-position with an alkoxy group.
Halo-S-triazinesCHEMONTID:0004639Aromatic compounds containing a 1,3,5-triazine ring that is substituted at the 2-position with a halogen atom.
2(hydroxyphenyl)acetic acidsCHEMONTID:0004644Phenylacetic acids that carry a hydroxyl group at the 2-position.
3(hydroxyphenyl)acetic acidsCHEMONTID:0004645Phenylacetic acids that carry a hydroxyl group at the 3-position.
o-AminophenolsCHEMONTID:0004654Phenols that are substituted with an amine group at the 2-position of the benzene ring.
m-AminophenolsCHEMONTID:0004655Phenols that are substituted with an amine group at the 3-position of the benzene ring.
p-AminophenolsCHEMONTID:0004656Phenols that are substituted with an amine group at the 4-position of the benzene ring.
Isoindole organothiophosphatesCHEMONTID:0004658Aromatic compounds containing an isoindole, which is N-substituted by an organothiophosphate group. Their general structure is R-CSP(=S)(OR')OR'', where R=isoindole, R',R\" = any atom.
Phosphorodithioic acid O-monoestersCHEMONTID:0004661Organooxygen compounds that contain a phosphorodithioic acid, which is O-monosubstituted by an organyl group.
Phosphorodithioic acid O,O-diestersCHEMONTID:0004662Organooxygen compounds that contain a phosphorodithioic acid, which is O,O-disubstituted by an organyl group.
NitroguanidinesCHEMONTID:0004667Organonitrogen compounds containing a nitro group, which is N-linked to a guanidine.
Nitrophenyl ethersCHEMONTID:0004671Aromatic compounds containing a nitrobenzene moiety that carries an ether group on the benzene ring.
Aryloxyphenoxypropionic acidsCHEMONTID:0004674Aromatic compounds containing a phenoxypropionic acid that is para-substituted with an aryl group.
Aryloxyphenoxypropionic acid estersCHEMONTID:0004675Aromatic compounds containing a phenoxypropionic acid ester that is para-substituted with an aryl group.
Alkyloxyphenoxypropionic acidsCHEMONTID:0004678Aromatic compounds containing a phenoxypropionic acid that is para-substituted with an alkyl group.
Alkyloxyphenoxypropionic acid estersCHEMONTID:0004679Aromatic compounds containing a phenoxypropionic acid ester that is para-substituted with an alkyl group.
HydroxybenzonitrilesCHEMONTID:0004680Aromatic containing a benzonitrile group moiety that carries an hydroxyl group on the benzene ring.
1,2,4-triazolopyrimidine-2-sulfonanilidesCHEMONTID:0004682Polycyclic aromatic compounds containing a 1,2,4-triazolo[1,5-a]pyrimidine ring system, which is substituted with a sulfonanilide at the 2-position.
Dioxoisoquinoline-4-carboxanilidesCHEMONTID:00046911,3-isoquinolinediones that are substituted at the ring 4-position with a carboxanilide.
1-benzothiophene-2-carboxanilidesCHEMONTID:0004692Aromatic heteropolycyclic compounds that contain a 1-benzothiophene ring system, which is substituted with an anilide at the 2-position.
S-alkylisothiosemicarbazonesCHEMONTID:0004694S-alkylated derivatives of isothiosemicarbazones.
4-halophenylacetic acidsCHEMONTID:0004697Aromatic compounds containing a phenylacetic acid, which is para-substituted with a halogen atom.
N-silyl compoundsCHEMONTID:0004698Organosilicon compounds containing at least one silicon-nitrogen bond.
Pyrimidinyl-2-sulfonylureasCHEMONTID:0004705Aromatic heterocyclic compounds containing a pyrimidine ring which is substituted with a sulfonylurea at the ring 2-position.
S-triazinyl-2-sulfonylureasCHEMONTID:0004706Aromatic heterocyclic compounds containing a s-triazine ring which is substituted with a urea at the ring 2-position.
6-substituted-2-pyridinylmethylaminesCHEMONTID:0004709Aromatic heterocyclic compounds contaning a pyridine ring which is substituted at the 2-position with a methylamine, and at the 6-position with any non-hydrogen atom.
Aromatic anilidesCHEMONTID:0004712Aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.
Hydrazinecarboxylic acid estersCHEMONTID:0004715Ester derivatives of hydrazinecarboxylic acids.
N-acylcarbazolesCHEMONTID:0004720Aromatic heteropolycyclic compounds containing a carbazole moiety, which is N-acylated.
Cyclic dithiocarbamic acid estersCHEMONTID:0004722Organosulfur cyclic compounds with the general formula R3SC(=S)N(R1)R2; R1-R2 = H or organyl group, R3 = organyl. Here, the dithiocarbamyl group is part of a ring.
Cyclohexene oximesCHEMONTID:0004723Cyclic compounds containing a oxime group which is substituted with a cyclohexene ring.
CyclopropylisoxazolesCHEMONTID:0004724Aromatic heterocyclic compounds containing an isoxazole ring substituted at one or more positions with a cyclopropyl group.
FormamidinesCHEMONTID:0004729Amidines with the general structure Amidines with the general structure RN=CHN(R')R\", where R, R',and R\" are any atoms not part of an amide or a thioamide group.
4-methoxy-1,2,3-triazinesCHEMONTID:0004732Aromatic heterocyclic compounds containing a 1,2,3-triazine ring, which is substituted at the 4-position with a methoxy group.
1,3,5-triazine-2,4-diaminesCHEMONTID:0004734Aromatic compounds containing a 1,3,5-triazine ring which is 2,4-disusbtituted wit amine groups.
Methylthio-s-triazinesCHEMONTID:0004735Aromatic compounds containing a 1,3,5-triazine ring that is substituted at the 2-position with a methylthio group.
PhenylenediaminesCHEMONTID:0004744Aromatic compound containing a benzene ring which carries 2 amino groups.
Aldoxime carbamatesCHEMONTID:0004753Oxime ether derivatives with the general formula CC(R)=NOC(=O)N(R')R\", where R=H, and R',R\" = H or organyl.
Ketoxime carbamatesCHEMONTID:0004754Oxime ether derivatives with the general formula CC(R)=NOC(=O)N(R')R\", where R=organyl, and R',R\" = H or organyl.
Furan-3-carboxylic acid and derivativesCHEMONTID:0004759Aromatic heterocyclic compounds containing a furan ring, which carries a carboxyl group or a derivative thereof at the ring 3-position.
Phenyl phenylphosphonothioatesCHEMONTID:0004767Aromatic compounds containing a phenylphosphonothioate group, which is O-esterified with another phenyl group. They have the general structure OP(R)(=S)OR', where R,R'=phenyl groups.
Phenyl ethylphosphonothioatesCHEMONTID:0004769Aromatic compounds containing a phenylphosphonothioate group, which is O-esterified with an ethyl group. They have the general structure OP(R)(=S)OR', where R=phenyl group, R' = ethyl group.
1,3,4-thiadiazol-3-yl-organothiophosphatesCHEMONTID:0004770Aromatic heterocyclic compounds containing a 1,3,4-thiadiazole ring, which is substituted at the 2-position with an organothiophosphate group.
Organic O-nitroso compoundsCHEMONTID:0004778Organic compounds containing a n-nitroso group -ON=O.
TrialkylglycerolsCHEMONTID:0004782Triradylglycerols that carry three chains attached to the glycerol moiety through ether linkages.
EpisulfonesCHEMONTID:0004783Sulfone derivatives containing the thiirane-1, 1-dione moiety.
Thiuram monosulfidesCHEMONTID:0004790Organic disulfides that have the general structural formula RN(R')C(=S)SCC(=S)N(R\")R\"', where R-R\"'=alkyl groups.
1,3-oxazolobenzo-1,4-diazepinesCHEMONTID:0004798Aromatic heteropolycyclic compounds containing a 1,3-oxazole ring fused to the 1,-4-diazepine moiety of a 1,4-benzodiazepine ring system.
5'-S-alkylthio-5'-deoxyribonucleosidesCHEMONTID:0004800A 5'-deoxyribonucleoside where the 5'-hydroxy group of the sugar moiety is substituted by a methylsulfanyl group.
2-benzylaminopyridinesCHEMONTID:0004802Aromatic compounds containing pyridine ring substituted at the 2-position by a benzylamine group.
BenzotropolonesCHEMONTID:0004804Organic aromatic polycyclic compounds containing a benzene ring fused to a tropolone.
Furoic acid estersCHEMONTID:0004805Ester derivatives of furoic acid.
MethoxidesCHEMONTID:0004807Compounds containing a methoxide group with the formula H3CO-.
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