NC1=NC2=C(N=CN2C2CC(O)C(CO)C2)C(Cl)=N1

InChIKey=KMURQHWZQUUEGV-UHFFFAOYSA-N

C11H14ClN5O2

283.72

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 Cyclopentanols Aryl chlorides Heteroaromatic compounds Cyclic alcohols and derivatives Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Organochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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