CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2F)C(=O)NC1=O.NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O

InChIKey=KFRDPGSGZWZXIK-ZIDZMDIJSA-N

C20H26FN7O9

527.466

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Pyrimidine 2'-deoxyribonucleosides Glycosylamines 6-aminopurines Aminopyrimidines and derivatives Pyrimidones Hydropyrimidines Imidolactams Monosaccharides N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Ureas Lactams Secondary alcohols Fluorohydrins Azacyclic compounds Oxacyclic compounds Primary alcohols Primary amines Hydrocarbon derivatives Alkyl fluorides Organic oxides Organofluorides

Not available

Purine nucleoside - Pyrimidine 2'-deoxyribonucleoside - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Pyrimidone - N-substituted imidazole - Hydropyrimidine - Pyrimidine - Monosaccharide - Imidolactam - Imidazole - Azole - Vinylogous amide - Heteroaromatic compound - Oxolane - Fluorohydrin - Halohydrin - Urea - Lactam - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Alkyl fluoride - Alkyl halide - Amine - Alcohol - Primary amine - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

Not available