Structural insights into IKKbeta inhibition by natural products staurosporine and quercetin

Bioorg Med Chem Lett. 2009 Dec 15;19(24):6907-10. doi: 10.1016/j.bmcl.2009.10.076. Epub 2009 Oct 22.

Abstract

This Letter describes the results of two combined approaches: homology modeling and molecular docking studies, in order to propose the molecular basis of IKKbeta inhibition by staurosporine and quercetin as ATP-competitive inhibitors. The results provides a rationale and structural frameworks for designing potent ATP binding-site inhibitors of IKKbeta, which is an attractive drug target for inflammatory diseases and has been found to be responsible for some of the already observed pharmacological effects for marketed drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemistry*
  • Biological Products / pharmacology
  • Drug Design
  • I-kappa B Kinase / antagonists & inhibitors*
  • Quercetin / chemistry*
  • Quercetin / pharmacology
  • Staurosporine / chemistry*
  • Staurosporine / pharmacology
  • Structure-Activity Relationship

Substances

  • Biological Products
  • Quercetin
  • I-kappa B Kinase
  • Staurosporine