OC(=O)CCC(O)=O.NC1=NC2=C(N=CN2[C@@H]2C[C@H](CO)C=C2)C(NC2CC2)=N1

InChIKey=BOONDNCXQPMXQT-SCYNACPDSA-N

C18H24N6O5

404.427

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 Secondary alkylarylamines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Dicarboxylic acids and derivatives Heteroaromatic compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives

Not available

1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Dicarboxylic acid or derivatives - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Secondary amine - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Alcohol - Organopnictogen compound - Organic nitrogen compound - 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