Structure Information
Structure

Compound Identification

SMILES

CC(C)(C)[C@@H](O)C(=O)NS(=O)(=O)OC[C@H]1C[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=YNANAXTWCZNKNG-RPLXWKFWSA-N

Formula

C17H26N6O7S

Mass

458.49

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Cyclopentyl nucleosides

Intermediate Tree Nodes

1,3-substituted cyclopentyl nucleosides

Direct Parent

1,3-substituted cyclopentyl purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Cyclopentanol - Pyrimidine - Imidolactam - Organic sulfuric acid or derivatives - Azole - Cyclic alcohol - Imidazole - Heteroaromatic compound - Secondary alcohol - Amino acid or derivatives - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine base.

External Descriptors

Not available

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