Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2C2CC(CO)C=C2)C(SC2CCC2)=N1

InChIKey

InChIKey=QUBFSQRMGGMJDC-UHFFFAOYSA-N

Formula

C15H19N5OS

Mass

317.41

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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-thiopurine - Imidazopyrimidine - Purine - Aryl thioether - Aminopyrimidine - Alkylarylthioether - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Primary amine - Amine - 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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