NC1=NC=NC2=C1N=CN2[C@@H]1C[C@@H](N=[N+]=[N-])[C@@H](O)[C@H]1O

InChIKey=UPIWCZFYODCBAS-APOSLCTFSA-N

C10H12N8O2

276.26

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 1,2-diols Azacyclic compounds Primary amines Organopnictogen compounds Organic zwitterions Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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