COC1=CC=C(C=NC2=NC(NC3CC3)=C3N=CN(C4CC(CO)C=C4)C3=N2)C=C1

InChIKey=DQIBFBKSAOABIR-UHFFFAOYSA-N

C22H24N6O2

404.474

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 Phenoxy compounds Methoxybenzenes Anisoles Aminopyrimidines and derivatives Alkyl aryl ethers N-substituted imidazoles Imidolactams Heteroaromatic compounds Shiff bases Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Amines

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Aminopyrimidine - Monocyclic benzene moiety - N-substituted imidazole - Imidolactam - Pyrimidine - Benzenoid - Heteroaromatic compound - Azole - Imidazole - Shiff base - Aldimine - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Azacycle - Ether - Primary alcohol - Organic nitrogen compound - Imine - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - 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