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Structure Information
Structure

Compound Identification

SMILES

OCC1OC(C(O)C1O)N1C(Cl)=C(C=O)C2=CC(Cl)=C(Cl)C=C12

InChIKey

InChIKey=QJLFDUROSXZMQK-UHFFFAOYSA-N

Formula

C14H12Cl3NO5

Mass

380.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Indole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Indole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-ribofuranosylindole - Glycosyl compound - N-glycosyl compound - N-alkylindole - Pentose monosaccharide - Indole - Indole or derivatives - Aryl-aldehyde - Aryl chloride - Aryl halide - Monosaccharide - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Oxolane - Pyrrole - Vinylogous amide - Vinylogous halide - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary alcohol - Aldehyde - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as indole ribonucleosides and ribonucleotides. These are compounds 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.

External Descriptors

Not available

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