A new class of pyrimidine nucleosides: inhibitors of hepatitis B and C viruses

Bioorg Med Chem Lett. 2012 Oct 15;22(20):6475-80. doi: 10.1016/j.bmcl.2012.08.042. Epub 2012 Aug 21.

Abstract

Hepatitis B virus (HBV) and hepatitis C virus (HCV) infections are major health threats worldwide leading to liver cirrhosis, liver cancer and mortality. Herein, we report a new category of dideoxy pyrimidine nucleosides possessing a 4'-carboxyl (or carboxymethyl) function (7-9, 13, 16, 17), which are discovered as potential antiviral agents. For the first time, these nucleosides are recognized to be inhibitors of HBV and/or HCV replication. Among 4'-carboxy compounds, 3',4'-didehydrothymidine (16) was most effective against DHBV, HBV and HCV. Modification of the 4'-position in compound 7 from a carboxyl to carboxymethyl group (17) did not affect the anti-HBV activity but greatly increased the anti-HCV activity. Importantly, 17 yielded synergistic antiviral effect when combined with ribavirin without toxicity. The activity exhibited by a single agent towards both hepatitis viruses and no detectable in vitro cytotoxicity make this new class of compounds of interest.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / chemistry*
  • Antiviral Agents / pharmacology*
  • Cell Line, Tumor
  • Hepacivirus / drug effects*
  • Hepatitis B / drug therapy
  • Hepatitis B / virology
  • Hepatitis B virus / drug effects*
  • Hepatitis C / drug therapy
  • Hepatitis C / virology
  • Humans
  • Liver / virology
  • Pyrimidine Nucleosides / chemistry*
  • Pyrimidine Nucleosides / pharmacology*

Substances

  • Antiviral Agents
  • Pyrimidine Nucleosides