Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=NC2=C(N=CN2[C@@H]2O[C@H](COC3=CC=C(C)C=C3)[C@@H](OC3=CC=C(C)C=C3)[C@H]2OC2=CC=C(C)C=C2)C(OC(=O)N(C2=CC=CC=C2)C2=CC=CC=C2)=N1

InChIKey

InChIKey=AQVSFQBWYBZTGU-FOQJVDBMSA-N

Formula

C46H42N6O7

Mass

790.877

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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 - Glycosyl compound - N-glycosyl compound - Phenylcarbamic acid ester - Hypoxanthine - Pentose monosaccharide - N-acetylarylamine - Imidazopyrimidine - Purine - Phenoxy compound - N-arylamide - Phenol ether - Alkyl aryl ether - Toluene - Monocyclic benzene moiety - Monosaccharide - Benzenoid - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Acetamide - Carbamic acid ester - Oxolane - Carboxamide group - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Oxacycle - Ether - Carboxylic acid derivative - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen 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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