CC(C)C(=O)NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1OCCNC(=O)C(F)(F)F

InChIKey=KBRJYHZINRIIRT-ORXWAGORSA-N

C18H23F3N6O7

492.412

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Glycosylamines 6-oxopurines Hypoxanthines N-arylamides Pyrimidones Monosaccharides N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Secondary carboxylic acid amides Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organopnictogen compounds Organofluorides Organic oxides Alkyl fluorides Primary alcohols Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Purine - Imidazopyrimidine - N-arylamide - Pyrimidone - N-substituted imidazole - Monosaccharide - Pyrimidine - Heteroaromatic compound - Oxolane - Azole - Imidazole - Vinylogous amide - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Alkyl halide - Hydrocarbon derivative - Organic oxide - Alkyl fluoride - Alcohol - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organohalogen compound - Organofluoride - Organonitrogen 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