CCOP(=O)(C[C@H]1C[C@H](ON1C)N1C=C(F)C(=O)NC1=O)OCC

InChIKey=IWHHYNDGPSCCFM-KOLCDFICSA-N

C13H21FN3O6P

365.298

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Phosphonated 2'-oxa,3'-aza pyrimidine nucleosides

Not available

Phosphonated 2'-oxa,3'-aza pyrimidine nucleosides

Pyrimidones Dialkyl alkylphosphonates Halopyrimidines Phosphonic acid esters Aryl fluorides Hydropyrimidines Vinylogous amides Heteroaromatic compounds Isoxazolidines Ureas Lactams Oxacyclic compounds Azacyclic compounds N-organohydroxylamines Hydrocarbon derivatives Organic oxides Organofluorides Organooxygen compounds Organophosphorus compounds Organopnictogen compounds

Aromatic heteromonocyclic compounds

Phosphonated 2'-oxa,3'-aza pyrimidine nucleoside - Halopyrimidine - Dialkyl alkylphosphonate - Phosphonic acid diester - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Isoxazolidine - Heteroaromatic compound - Organophosphonic acid derivative - Vinylogous amide - Lactam - Urea - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organonitrogen compound - Organofluoride - Organic nitrogen compound - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organophosphorus compound - Organic oxygen compound - Organopnictogen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as phosphonated 2'-oxa,3'-aza pyrimidine nucleosides. These are nucleoside and nucleotide analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-aza derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides. Moreover, a phosphonate group s attached to the C4-atom of the resulting 1.3-oxazolidine.

Not available