Structure Information
Structure

Compound Identification

SMILES

CN1C=C(C2=CC=CC=C12)C1=C(C(=O)NC1=O)C1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C2=CC=CC=C12

InChIKey

InChIKey=PMCKEKSLSVBFRE-VJUOEERUSA-N

Formula

C26H23N3O6

Mass

473.485

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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 - Maleimide - Monosaccharide - N-methylpyrrole - Substituted pyrrole - Benzenoid - Carboxylic acid imide - Dicarboximide - Heteroaromatic compound - Carboxylic acid imide, n-unsubstituted - Oxolane - Pyrrole - Pyrroline - 1,2-diol - Secondary alcohol - Azacycle - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Alcohol - Primary alcohol - Organic oxygen compound - Organic oxide - Organic nitrogen 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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