Structure Information
Structure

Compound Identification

SMILES

COC1=NC=NC2=C1N=CN2[C@@H]1C[C@H](CO)[C@@H]2C[C@H]12

InChIKey

InChIKey=LRZCATIJDBONEC-XFWSIPNHSA-N

Formula

C13H16N4O2

Mass

260.297

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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 - Hypoxanthine - Imidazopyrimidine - Purine - Alkyl aryl ether - Pyrimidine - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Primary alcohol - Organonitrogen compound - Organooxygen compound - 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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