CCO[P+]([O-])(C[C@@H]1C[C@@H](ON1C)N1C=C(C)C(=O)NC1=O)OCC

InChIKey=MVAZAYVUDUJZAB-NWDGAFQWSA-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 Organooxygen compounds Hydrocarbon derivatives Organic zwitterions Organic oxides Organophosphorus 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 - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Organic zwitterion - 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