Synthesis of new 2'-beta-C-methyl related triciribine analogues as anti-HCV agents

Bioorg Med Chem Lett. 2004 Jul 5;14(13):3517-20. doi: 10.1016/j.bmcl.2004.04.067.

Abstract

Ten new beta-D-ribofuranosyl and 2'-beta-C-methyl-beta-D-ribofuranosyl triciribine derivatives 4-13 with various N4 and 6-N substituents on the tricyclic ring were synthesized from the corresponding toyocamycin and new 2'-beta-C-methyl toyocamycin derivatives. The inhibitory studies of these compounds in the HCV replicon assay reveal that some of them possess interesting anti-HCV properties with low cytotoxicity.

MeSH terms

  • Animals
  • Antiviral Agents / chemical synthesis*
  • Antiviral Agents / pharmacology
  • Cells, Cultured
  • Cytotoxicity Tests, Immunologic
  • Hepacivirus / drug effects*
  • Hepacivirus / enzymology
  • Hepacivirus / physiology
  • Molecular Structure
  • Ribonucleosides / chemical synthesis*
  • Ribonucleosides / pharmacology
  • Virus Replication / drug effects*

Substances

  • Antiviral Agents
  • Ribonucleosides
  • triciribine