NC1=NC2=C(N=CN2[C@@H]2C[C@H](CO)[C@H]3O[C@@H]23)C(Cl)=N1

InChIKey=USHJATVFQUWQAM-APOSLCTFSA-N

C11H12ClN5O2

281.7

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 Oxanes N-substituted imidazoles Aryl chlorides Heteroaromatic compounds Oxacyclic compounds Epoxides Dialkyl ethers Azacyclic compounds Primary amines Primary alcohols Organochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - Purine - Imidazopyrimidine - Aminopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Pyrimidine - N-substituted imidazole - Oxane - Heteroaromatic compound - Azole - Imidazole - Oxacycle - Dialkyl ether - Oxirane - Ether - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Amine - Alcohol - Primary amine - Primary alcohol - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - 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