Structure Information
Structure

Compound Identification

SMILES

CNC(=O)[C@@]12C[C@@H]1[C@H]([C@H](O)[C@@H]2O)N1C=NC2=C1N=C(Cl)N=C2NCC1=CC(Cl)=CC=C1

InChIKey

InChIKey=GAYWHRPOIWFKIF-DDDALXFXSA-N

Formula

C20H20Cl2N6O3

Mass

463.32

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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-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Benzylamine - Aminopyrimidine - 2-halopyrimidine - Chlorobenzene - Halobenzene - Halopyrimidine - Secondary aliphatic/aromatic amine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Cyclopropanecarboxylic acid or derivatives - N-substituted imidazole - Pyrimidine - Imidolactam - Benzenoid - Azole - Cyclic alcohol - Heteroaromatic compound - Imidazole - 1,2-diol - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Amino acid or derivatives - Azacycle - Secondary amine - Carboxylic acid derivative - Organoheterocyclic compound - Organochloride - Carbonyl group - Organopnictogen compound - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Organohalogen compound - Organic oxide - 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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