Identification and biological activity of 6-alkyl-substituted 3-methyl-pyridine-2-carbonyl amino dimethyl-benzoic acid EP4 antagonists

Bioorg Med Chem Lett. 2016 May 1;26(9):2303-7. doi: 10.1016/j.bmcl.2016.03.041. Epub 2016 Mar 12.

Abstract

Continued SAR optimization of a series of 3-methylpyridine-2-carbonyl amino-2,4-dimethyl-benzoic acid led to the selection of compound 4f for clinical studies. Compound 4f showed an IC50 of 123nM for inhibition of PGE2-induced TNFα reduction in an ex vivo LPS-stimulated human whole blood assay (showing >10-fold increase over clinical compound CJ-023,423). Pharmacokinetic profile, selectivity and in vivo efficacy comparing 4f to NSAID diclofenac in the monoiodoacetic acid (MIA) pain model and adjuvant induced arthritis (AIA) inflammatory model are included.

Keywords: Clinical candidate; EP4 antagonist; Inflammation; Pain; Prostaglandin E2 (PGE2).

MeSH terms

  • Animals
  • Benzoates / chemistry
  • Benzoates / pharmacology*
  • Rats
  • Receptors, Prostaglandin E, EP4 Subtype / antagonists & inhibitors*
  • X-Ray Diffraction

Substances

  • Benzoates
  • Receptors, Prostaglandin E, EP4 Subtype