Cl.NC1=NC=NC2=C1N=CN2[C@@H]1C[C@H](NO)[C@@H](O)[C@H]1O

InChIKey=OWEFVASYSWZFDS-RDSGXXSDSA-N

C10H15ClN6O3

302.72

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Cyclopentanols Heteroaromatic compounds Cyclic alcohols and derivatives 1,2-diols N-organohydroxylamines Azacyclic compounds Primary amines Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Cyclopentanol - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Cyclic alcohol - Secondary alcohol - 1,2-diol - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrochloride - Hydrocarbon derivative - Organopnictogen compound - Amine - Alcohol - Organic oxygen 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