NC1=NC=NC2=C1N=CN2C1CC(CO)C(O)C1N=[N+]=[N-]

InChIKey=PRAZYXWKEDCLBZ-UHFFFAOYSA-N

C11H14N8O2

290.287

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 Azo imides Azo compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Organic zwitterions Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Cyclopentanol - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Cyclic alcohol - Imidazole - Heteroaromatic compound - Secondary alcohol - Azo compound - Azo imide - Organoheterocyclic compound - Azacycle - Organic zwitterion - Hydrocarbon derivative - Amine - Organopnictogen compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organonitrogen 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