COC1=CC(=O)\C(=C\NC2=NC3=C(N=CN3[C@@H]3C[C@H](CO)C=C3)C(NC3CC3)=N2)C=C1

InChIKey=QMFZCGSLWDYOBZ-VRCKCISPSA-N

C22H24N6O3

420.473

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 O-quinomethanes Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Vinylogous esters Vinylogous amides Heteroaromatic compounds Enamines Azacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - O-quinomethane - Quinomethane - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Vinylogous ester - Vinylogous amide - Ketone - Cyclic ketone - Enamine - Azacycle - Organoheterocyclic compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - 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