Cl.Cl.NC1=NC2=C(N=CN2C2CC(CO)C=C2)C(=N1)N1CCCCC1

InChIKey=QXFDZOLWEAMPLD-UHFFFAOYSA-N

C16H24Cl2N6O

387.31

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Cyclopentyl nucleosides

1,3-substituted cyclopentyl nucleosides

1,3-substituted cyclopentyl purine nucleosides

6-alkylaminopurines Dialkylarylamines Aminopyrimidines and derivatives Piperidines N-substituted imidazoles Imidolactams Heteroaromatic compounds Azacyclic compounds Primary amines Primary alcohols Hydrochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Pyrimidine - Piperidine - Azole - Heteroaromatic compound - Imidazole - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrochloride - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Primary amine - 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