Ribavirin antagonizes the in vitro anti-hepatitis C virus activity of 2'-C-methylcytidine, the active component of valopicitabine

Antimicrob Agents Chemother. 2006 Oct;50(10):3444-6. doi: 10.1128/AAC.00372-06.

Abstract

Ribavirin antagonizes the in vitro anti-hepatitis C virus (HCV) activity of the pyrimidine nucleoside analogue 2'-C-methylcytidine, the active component of the experimental anti-HCV drug valopicitabine. In contrast, the combination of ribavirin with either the purine nucleoside analogue 2'-C-methyladenosine or the HCV protease inhibitor VX-950 resulted in an additive antiviral activity. These findings may have implications when planning clinical studies with valopicitabine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / antagonists & inhibitors*
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Cell Line, Tumor
  • Cytidine / analogs & derivatives*
  • Cytidine / antagonists & inhibitors
  • Drug Antagonism
  • Drug Therapy, Combination
  • Hepacivirus / drug effects*
  • Hepacivirus / physiology
  • Humans
  • Ribavirin / pharmacology*
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • 2'-C-methylcytidine
  • Ribavirin
  • Cytidine