Aminopyridinecarboxamide-based inhibitors: Structure-activity relationship

Bioorg Med Chem. 2010 Jan 1;18(1):403-14. doi: 10.1016/j.bmc.2009.10.040. Epub 2009 Oct 27.

Abstract

Series of aminopyridinecarboxamide-based inhibitors were synthesized and tested against human recombinant IKK-2 and in IL-1beta stimulated synovial fibroblasts. The 2-amino-5-chloropyridine-4-carboxamides were identified as the most potent inhibitors with improved cellular activity.

MeSH terms

  • Amides / chemistry
  • Amides / pharmacology
  • Amino Acid Sequence
  • Aminopyrine / chemistry*
  • Aminopyrine / pharmacology*
  • Anti-Inflammatory Agents / chemistry*
  • Anti-Inflammatory Agents / pharmacology*
  • Arthritis, Rheumatoid / drug therapy
  • Fibroblasts / drug effects
  • Fibroblasts / immunology
  • Humans
  • I-kappa B Kinase / antagonists & inhibitors*
  • I-kappa B Kinase / metabolism
  • I-kappa B Proteins / chemistry
  • Interleukin-1beta / antagonists & inhibitors*
  • Interleukin-1beta / metabolism
  • Joint Capsule / cytology
  • Molecular Sequence Data
  • Structure-Activity Relationship

Substances

  • Amides
  • Anti-Inflammatory Agents
  • I kappa B beta protein
  • I-kappa B Proteins
  • Interleukin-1beta
  • Aminopyrine
  • I-kappa B Kinase