Synthesis and in vitro anti-hepatitis B and C virus activities of ring-expanded ('fat') nucleobase analogues containing the imidazo[4,5-e][1,3]diazepine-4,8-dione ring system

Bioorg Med Chem Lett. 2005 Dec 15;15(24):5397-401. doi: 10.1016/j.bmcl.2005.09.015. Epub 2005 Oct 5.

Abstract

As part of our structure-activity relationship studies, we report here the synthesis and in vitro anti-HBV and anti-HCV activities of a number of ring-expanded ('fat') nucleobases containing the imidazo[4,5-e][1,3]diazepine-4,8-dione ring system. One of the compounds, ZP-88, exhibited a good activity/toxicity profile against HBV by inhibition of the synthesis of extracellular virion release (EC(50)=1.7microM, CC(50)=286microM, SI=168) and intracellular HBV replication intermediates (EC(50)=8.4microM, CC(50)=286microM, SI=34) in cultured human hepatoblastoma 2.2.15 cells. By contrast, most of the compounds tested against HCV had only marginal activity/toxicity profile, although that was still better than that of the reference compound ribavirin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / pharmacology*
  • Benzazepines / chemical synthesis*
  • Benzazepines / pharmacology*
  • Hepacivirus / drug effects*
  • Hepatitis B / drug therapy
  • Hepatitis B virus / drug effects*
  • Hepatitis C / drug therapy
  • Humans
  • Imidazoles / chemical synthesis
  • Imidazoles / pharmacology
  • Nucleosides / chemical synthesis
  • Nucleosides / pharmacology*
  • Virion / drug effects

Substances

  • Antiviral Agents
  • Benzazepines
  • Imidazoles
  • Nucleosides