NC1=NC2=C(N(CC=C)C(=O)N2C2CCC(CO)C2)C(Cl)=N1

InChIKey=HWNYTERDUPJLRW-UHFFFAOYSA-N

C14H18ClN5O2

323.78

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

Purinones Halopyrimidines Aminopyrimidines and derivatives N-substituted imidazoles Aryl chlorides Heteroaromatic compounds Ureas Azacyclic compounds Primary amines Primary alcohols Organochlorides Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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