Structure Information
Structure

Compound Identification

SMILES

OCC1CC(C(O)C1O)N1C=NC2=C1N=CN=C2Cl

InChIKey

InChIKey=GGJDZOWNXFYEEV-UHFFFAOYSA-N

Formula

C11H13ClN4O3

Mass

284.7

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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 - Purine - Imidazopyrimidine - Halopyrimidine - Pyrimidine - N-substituted imidazole - Cyclopentanol - Aryl halide - Aryl chloride - Heteroaromatic compound - Imidazole - Cyclic alcohol - Azole - Secondary alcohol - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - 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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