Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=CC=C(OCC(O)CSC2=NC3=C(NC=NC3=O)N2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=C1

InChIKey

InChIKey=OPMNXDIOWKLIPD-LUKQQSODSA-N

Formula

C22H26N4O9S

Mass

522.53

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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 - N-glycosyl compound - Glycosyl compound - 6-oxopurine - Pentose monosaccharide - Hypoxanthine - Benzoate ester - Purine - Imidazopyrimidine - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Aryl thioether - Benzoyl - Alkyl aryl ether - Alkylarylthioether - Pyrimidone - Benzenoid - Monosaccharide - N-substituted imidazole - Pyrimidine - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Vinylogous amide - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - Carboxylic acid ester - Thioether - Oxacycle - Carboxylic acid derivative - Sulfenyl compound - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary alcohol - Organic oxide - Alcohol - 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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