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Structure Information
Structure

Compound Identification

SMILES

NC(=O)N\N=C\C1=C(Cl)N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C2=CC(Cl)=C(Cl)C=C12

InChIKey

InChIKey=ZIMFOVRECXJPIO-IMWZBCAKSA-N

Formula

C15H15Cl3N4O5

Mass

437.66

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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 - Pentose monosaccharide - N-alkylindole - Indole - Indole or derivatives - Aryl chloride - Aryl halide - Monosaccharide - Benzenoid - Substituted pyrrole - Semicarbazone - Oxolane - Heteroaromatic compound - Semicarbazide - Pyrrole - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Organohalogen compound - Primary alcohol - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - 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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