Design, synthesis and structure-activity relationships of a novel class of sulfonylpyridine inhibitors of Interleukin-2 inducible T-cell kinase (ITK)

Bioorg Med Chem Lett. 2014 Dec 15;24(24):5818-5823. doi: 10.1016/j.bmcl.2014.10.020. Epub 2014 Oct 12.

Abstract

Starting from benzylpyrimidine 2, molecular modeling and X-ray crystallography were used to design highly potent inhibitors of Interleukin-2 inducible T-cell kinase (ITK). Sulfonylpyridine 4i showed sub-nanomolar affinity against ITK, was selective versus Lck and its activity in the Jurkat cell-based assay was greatly improved over 2.

Keywords: ITK inhibitor; Sulfonylpyridine; T-cell receptor.

MeSH terms

  • Binding Sites
  • Crystallography, X-Ray
  • Drug Design*
  • Kinetics
  • Molecular Dynamics Simulation
  • Protein Binding
  • Protein Kinase Inhibitors / chemical synthesis*
  • Protein Kinase Inhibitors / chemistry
  • Protein Kinase Inhibitors / metabolism
  • Protein Structure, Tertiary
  • Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Protein-Tyrosine Kinases / metabolism
  • Pyrazoles / chemistry
  • Pyridines / chemical synthesis
  • Pyridines / chemistry*
  • Pyridines / metabolism
  • Structure-Activity Relationship
  • Sulfones / chemistry

Substances

  • Protein Kinase Inhibitors
  • Pyrazoles
  • Pyridines
  • Sulfones
  • pyrazole
  • Protein-Tyrosine Kinases
  • emt protein-tyrosine kinase
  • pyridine