Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CN2C=C(CCNC3=NC=NC4=C3N=CN4[C@@H]3O[C@@H]([C@@H](O)[C@H]3O)C(=O)NC3CC3)C3=CC=CC=C23)C=C1

InChIKey

InChIKey=GPGSUWUFGSVNLL-OVDFTCDZSA-N

Formula

C31H33N7O5

Mass

583.649

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - 3-alkylindole - N-alkylindole - Imidazopyrimidine - Purine - Indole or derivatives - Indole - Methoxybenzene - Phenoxy compound - Phenol ether - Anisole - Aminopyrimidine - Alkyl aryl ether - Substituted pyrrole - N-substituted imidazole - Pyrimidine - Benzenoid - Imidolactam - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Pyrrole - Oxolane - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Oxacycle - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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