CCOP(=O)(CO[C@H]1C[C@H](C=C1)N1C=C(C)C(=O)NC1=O)OCC

InChIKey=YZJVHQYHPCXQNO-QWHCGFSZSA-N

C15H23N2O6P

358.331

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

Pyrimidones Dialkyl alkylphosphonates Phosphonic acid esters Hydropyrimidines Vinylogous amides Heteroaromatic compounds Ureas Lactams Azacyclic compounds Organophosphorus compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

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