Structure Information
Structure

Compound Identification

SMILES

OC1C(COC(=S)NC2CCCC2OCC2=CC=CC=C2)OC(C1O)N1C=NC2=C1N=CN=C2NC1CCOC1

InChIKey

InChIKey=AUCDFDZQUDBEOK-UHFFFAOYSA-N

Formula

C27H34N6O6S

Mass

570.67

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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 - 6-alkylaminopurine - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Benzylether - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Monocyclic benzene moiety - Imidolactam - Benzenoid - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Oxolane - Thiocarbamic acid ester - 1,2-diol - Thiocarbamic acid derivative - Secondary alcohol - Oxacycle - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organopnictogen compound - Organosulfur compound - 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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