CCOP(=O)(CC1CC(ON1C)N1C=CC(N)NC1=O)OCC

InChIKey=UJYXZZQTMDYNSM-UHFFFAOYSA-N

C13H25N4O5P

348.34

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 Aminopyrimidines and derivatives Dialkyl alkylphosphonates Phosphonic acid esters Hydropyrimidines Isoxazolidines Ureas Oxacyclic compounds Azacyclic compounds N-organohydroxylamines Organophosphorus compounds Hydrocarbon derivatives Organopnictogen compounds Organic oxides Monoalkylamines Carbonyl compounds

Aliphatic heteromonocyclic compounds

Phosphonated 2'-oxa,3'-aza pyrimidine nucleoside - Aminopyrimidine - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Hydropyrimidine - 1,2,3,4-tetrahydropyrimidine - Phosphonic acid ester - Pyrimidine - Isoxazolidine - Organophosphonic acid derivative - Carbonic acid derivative - Urea - N-organohydroxylamine - Azacycle - Oxacycle - Organoheterocyclic compound - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Aliphatic 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