Structural factors contributing to the Abl/Lyn dual inhibitory activity of 3-substituted benzamide derivatives

Bioorg Med Chem Lett. 2007 May 15;17(10):2712-7. doi: 10.1016/j.bmcl.2007.03.002. Epub 2007 Mar 3.

Abstract

To investigate why 3-substituted benzamide derivatives show dual inhibition of Abl and Lyn protein tyrosine kinases, we determined their inhibitory activities against Abl and Lyn, carried out molecular modeling, and conducted a structure-activity relationship study with the aid of a newly determined X-ray structure of the Abl/Lyn dual inhibitor INNO-406 (formerly known as NS-187) bound to human Abl. We found that this series of compounds interacted with both kinases in very similar ways, so that they can inhibit both kinases effectively.

MeSH terms

  • Benzamides / chemistry
  • Benzamides / pharmacology*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Molecular Conformation
  • Proto-Oncogene Proteins c-abl / antagonists & inhibitors*
  • Pyrimidines / chemistry
  • Pyrimidines / pharmacology*
  • Structure-Activity Relationship
  • src-Family Kinases / antagonists & inhibitors*

Substances

  • Benzamides
  • Enzyme Inhibitors
  • Pyrimidines
  • benzamide
  • Proto-Oncogene Proteins c-abl
  • lyn protein-tyrosine kinase
  • src-Family Kinases
  • bafetinib