Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)C(=O)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1OC1(C2=CC=CC=C2)C2=CC=CC=C2OC2=CC=CC=C12

InChIKey

InChIKey=SRLJSLYWCOWDBX-BEGXHNNXSA-N

Formula

C37H31N5O7

Mass

657.683

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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 - Dibenzopyran - Xanthene - N-glycosyl compound - Glycosyl compound - Diaryl ether - Benzopyran - 1-benzopyran - Imidazopyrimidine - Benzamide - Benzoic acid or derivatives - Purine - Benzylether - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Benzoyl - Alkyl aryl ether - Monocyclic benzene moiety - Monosaccharide - Pyrimidine - Imidolactam - N-substituted imidazole - Benzenoid - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Primary alcohol - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - 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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