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

InChIKey=CEEVPDLZRBSVGO-AVGNSLFASA-N

C15H25N2O7P

376.346

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Phosphonated cyclopentyl nucleosides

1,3-substituted phosphonated cyclopentyl nucleosides

1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides

Cyclopentyl nucleosides Pyrimidones Dialkyl alkylphosphonates Cyclopentanols Phosphonic acid esters Hydropyrimidines Vinylogous amides Heteroaromatic compounds Cyclic alcohols and derivatives Ureas Lactams Azacyclic compounds Organonitrogen compounds Organophosphorus compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides

Aromatic heteromonocyclic compounds

1,3-substituted phosphonated cyclopentyl pyrimidine nucleoside - Cyclopentyl nucleoside - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Cyclopentanol - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Cyclic alcohol - Organophosphonic acid derivative - Heteroaromatic compound - Vinylogous amide - Lactam - Secondary alcohol - Urea - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Alcohol - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 1,3-substituted phosphonated cyclopentyl pyrimidine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 3-position with either a pyrimidine base.

Not available