[Cl-].[NH3+]C1=NC2=C(N=CN2[C@@H]2C[C@H](CO)C=C2)C(Cl)=N1

InChIKey=VZJFPECAPXUELG-HHQFNNIRSA-N

C11H13Cl2N5O

302.16

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

Purines and purine derivatives Halopyrimidines Aminopyrimidines and derivatives N-substituted imidazoles Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary alcohols Organochlorides Organic zwitterions Organic chloride salts Hydrocarbon derivatives Amines

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - Imidazopyrimidine - Purine - Aminopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic zwitterion - Organic salt - Amine - Organic chloride salt - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteropolycyclic compound

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.

Not available