O[C@@H]1[C@@H](COC2=CC(F)=CC=C2)OC([C@@H]1O)N1C=NC2=C1N=CN=C2NC1CCOC1

InChIKey=DMXJNVKAUIRESA-YPCFTJQESA-N

C20H22FN5O5

431.424

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-alkylaminopurines Glycosylamines Phenoxy compounds Phenol ethers Secondary alkylarylamines Alkyl aryl ethers Fluorobenzenes Aminopyrimidines and derivatives N-substituted imidazoles Monosaccharides Imidolactams Aryl fluorides Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organofluorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - N-glycosyl compound - Glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Phenoxy compound - Phenol ether - Halobenzene - Alkyl aryl ether - Aminopyrimidine - Fluorobenzene - Secondary aliphatic/aromatic amine - Monosaccharide - N-substituted imidazole - Aryl fluoride - Aryl halide - Imidolactam - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Heteroaromatic compound - Oxolane - Azole - Imidazole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Secondary amine - Dialkyl ether - Ether - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organooxygen compound - Amine - Organic nitrogen compound - Organonitrogen compound - Organofluoride - Organohalogen 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