Structure Information
Structure

Compound Identification

SMILES

CN(C)CCOC(=O)C1=CC=C(OCC(O)CSC2=NC3=C(N=CN=C3N)N2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C=C1

InChIKey

InChIKey=MOYFNFWRLXGKPN-SEQHXNGFSA-N

Formula

C24H32N6O8S

Mass

564.61

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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 - 6-aminopurine - Benzoate ester - Pentose monosaccharide - Benzoic acid or derivatives - Imidazopyrimidine - Purine - Phenoxy compound - Aryl thioether - Benzoyl - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Alkylarylthioether - Monocyclic benzene moiety - Imidolactam - Monosaccharide - N-substituted imidazole - Benzenoid - Pyrimidine - Oxolane - Azole - Heteroaromatic compound - Imidazole - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Tertiary aliphatic amine - Carboxylic acid ester - Sulfenyl compound - Thioether - Oxacycle - Carboxylic acid derivative - Ether - Azacycle - Organoheterocyclic compound - Organic oxide - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Amine - Organosulfur compound - Primary amine - Organic oxygen compound - 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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