Design, synthesis, and antiviral properties of 4'-substituted ribonucleosides as inhibitors of hepatitis C virus replication: the discovery of R1479

Bioorg Med Chem Lett. 2007 May 1;17(9):2570-6. doi: 10.1016/j.bmcl.2007.02.004. Epub 2007 Feb 4.

Abstract

A series of 4'-substituted ribonucleoside derivatives has been prepared and evaluated for inhibition of hepatitis C virus (HCV) RNA replication in cell culture. The most potent and non-cytotoxic derivative was compound 28 (4'-azidocytidine, R1479) with an IC(50) of 1.28 microM in the HCV replicon system. The triphosphate of compound 28 was prepared and shown to be an inhibitor of RNA synthesis mediated by NS5B (IC(50)=320 nM), the RNA polymerase encoded by HCV. Data on related analogues have been used to generate some preliminary requirements for activity within this series of nucleosides.

MeSH terms

  • Antiviral Agents / chemistry*
  • Chemistry, Pharmaceutical / methods*
  • Cytidine / analogs & derivatives*
  • Cytidine / pharmacology
  • Drug Design
  • Drug Evaluation, Preclinical
  • Hepacivirus / genetics*
  • Inhibitory Concentration 50
  • Models, Chemical
  • Molecular Conformation
  • Nucleosides / chemistry
  • RNA / chemistry
  • Ribonucleosides / chemistry*
  • Uridine
  • Virus Replication / drug effects*

Substances

  • Antiviral Agents
  • Nucleosides
  • Ribonucleosides
  • Cytidine
  • RNA
  • 4'-azidocytidine
  • Uridine