Pyridinylimidazole based p38 MAP kinase inhibitors

Curr Top Med Chem. 2002 Sep;2(9):1011-20. doi: 10.2174/1568026023393372.

Abstract

The p38 MAP kinase is thought to be involved in a variety of inflammatory and immunological disorders such as rheumatoid arthritis. The pyridinylimidazole class of compounds was the first to potently inhibit this kinase. Since the original reports of their efficacy, they have become the most widely studied series of inhibitors of this kinase. This framework has served as a starting point for further synthetic work and several compounds have entered clinical trials. These compounds have also been utilized to elucidate the role of p38 kinase in the immune system, and more recently have been used to examine the role of this kinase in central nervous system disorders.

Publication types

  • Review

MeSH terms

  • Animals
  • Antirheumatic Agents / chemistry
  • Antirheumatic Agents / pharmacology
  • Arthritis, Experimental / drug therapy
  • Drug Design
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Imidazoles / chemistry*
  • Imidazoles / pharmacology*
  • Indoles / chemistry
  • Indoles / pharmacology
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors*
  • Mitogen-Activated Protein Kinases / immunology
  • Mitogen-Activated Protein Kinases / metabolism
  • Oxazoles / chemistry
  • Oxazoles / pharmacology
  • Pyridines / chemistry*
  • Pyridines / pharmacology*
  • Structure-Activity Relationship
  • Thiazoles / chemistry
  • Thiazoles / pharmacology
  • Tumor Cells, Cultured / drug effects
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Antirheumatic Agents
  • Enzyme Inhibitors
  • Imidazoles
  • Indoles
  • Oxazoles
  • Pyridines
  • Thiazoles
  • indole
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases