Pyrroles and other heterocycles as inhibitors of p38 kinase

Bioorg Med Chem Lett. 1998 Oct 6;8(19):2689-94. doi: 10.1016/s0960-894x(98)00495-8.

Abstract

Investigation of furans, pyrroles and pyrazolones identified 3-pyridyl-2,5-diaryl-pyrroles as potent, orally bioavailable inhibitors of p38 kinase. 3-(4-pyridyl-2-(4-fluoro-phenyl)-5-(4-methylsulfinylphenyl)-pyrrol e (L-167307) reduces secondary paw swelling in the rat adjuvant arthritis model: ID50 = 7.4 mg/kg/b.i.d.

MeSH terms

  • Animals
  • Arthritis, Experimental / drug therapy
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors*
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / pharmacokinetics
  • Enzyme Inhibitors / pharmacology*
  • Furans / chemical synthesis
  • Furans / pharmacokinetics
  • Furans / pharmacology*
  • Humans
  • Mitogen-Activated Protein Kinases*
  • Pyrazoles / chemical synthesis
  • Pyrazoles / pharmacokinetics
  • Pyrazoles / pharmacology*
  • Pyrroles / chemical synthesis
  • Pyrroles / pharmacokinetics
  • Pyrroles / pharmacology*
  • Rats
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Enzyme Inhibitors
  • Furans
  • Pyrazoles
  • Pyrroles
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases