Synthesis and biological evaluation of tricyclic anilinopyrimidines as IKKbeta inhibitors

Bioorg Med Chem Lett. 2010 Jun 15;20(12):3821-5. doi: 10.1016/j.bmcl.2010.04.022. Epub 2010 Apr 18.

Abstract

A series of tricyclic anilinopyrimidines were synthesized and evaluated as IKKbeta inhibitors. Several analogues, including tricyclic phenyl (10, 18a, 18c, 18d, and 18j) and thienyl (26 and 28) derivatives were shown to have good in vitro enzyme potency and excellent cellular activity. Pharmaceutical profiling of a select group of tricyclic compounds compared to the non-tricyclic analogues suggested that in some cases, the improved cellular activity may be due to increased clog P and permeability.

MeSH terms

  • Animals
  • Cell Line
  • Cell Membrane Permeability
  • Cell Proliferation / drug effects
  • Humans
  • I-kappa B Kinase / antagonists & inhibitors*
  • Inhibitory Concentration 50
  • Pyrimidines / chemical synthesis*
  • Pyrimidines / pharmacology*
  • Structure-Activity Relationship

Substances

  • Pyrimidines
  • I-kappa B Kinase