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

InChIKey=MVAZAYVUDUJZAB-NEPJUHHUSA-N

C14H24N3O6P

361.335

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 Phosphonic acid esters Hydropyrimidines Vinylogous amides Heteroaromatic compounds Isoxazolidines Ureas Lactams Azacyclic compounds Oxacyclic compounds N-organohydroxylamines Organophosphorus compounds Hydrocarbon derivatives Organooxygen compounds Organic oxides Organopnictogen compounds

Aromatic heteromonocyclic compounds

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