Structure Information
Structure

Compound Identification

SMILES

CC(=O)N(C1=NC2=C(N=C(N)N=C2OC(=O)OCC2C3=CC=CC=C3C3=CC=CC=C23)N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C1=CC2=C(C=C1)C1=CC=CC=C1C2

InChIKey

InChIKey=OWDLNAGVFKJPKK-SPBWOXKUSA-N

Formula

C40H34N6O8

Mass

726.746

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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 - Fluorene - Glycosyl compound - N-glycosyl compound - Hypoxanthine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Carbonic acid diester - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Acetamide - Tertiary carboxylic acid amide - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Carbonic acid derivative - Amino acid or derivatives - Carboxamide group - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Primary amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Alcohol - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Primary alcohol - 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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