The inhibitor of cyclin-dependent kinases, olomoucine II, exhibits potent antiviral properties

Antivir Chem Chemother. 2010 Jan 5;20(3):133-42. doi: 10.3851/IMP1460.

Abstract

Background: Olomoucine II, the most recent derivative of roscovitine, is an exceptionally potent pharmacological inhibitor of cyclin-dependent kinase activities. Here, we report that olomoucine II is also an effective antiviral agent.

Methods: Antiviral activities of olomoucine II were tested on a range of human viruses in in vitro assays that evaluated viral growth and replication.

Results: Olomoucine II inhibited replication of a broad range of wild-type human viruses, including herpes simplex virus, human adenovirus type-4 and human cytomegalovirus. Olomoucine II also inhibited replication of vaccinia virus and herpes simplex virus mutants resistant to conventional acyclovir treatment. This report is the first demonstration of a poxvirus being sensitive to a cyclin-dependent kinase inhibitor. The antiviral effects of olomoucine II could be observed at lower concentrations than with roscovitine, although both were short-term. A remarkable observation was that olomoucine II, when used in combination with the DNA polymerase inhibitor cidofovir, was able to almost completely eliminate the spread of infectious adenovirus type-4 progeny from infected cells.

Conclusions: Our results show that when targeting two complementary antiviral mechanisms, strongly additive effects could be observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / pharmacology*
  • Cyclin-Dependent Kinases / antagonists & inhibitors*
  • Humans
  • Inhibitory Concentration 50
  • Protein Kinase Inhibitors / pharmacology*
  • Purines / pharmacology*
  • Virus Physiological Phenomena / drug effects
  • Virus Replication / drug effects
  • Viruses / enzymology*
  • Viruses / growth & development

Substances

  • Antiviral Agents
  • Protein Kinase Inhibitors
  • Purines
  • olomoucine II
  • Cyclin-Dependent Kinases