Design and synthesis of substituted pyridine derivatives as HIF-1alpha prolyl hydroxylase inhibitors

Bioorg Med Chem Lett. 2006 Nov 1;16(21):5616-20. doi: 10.1016/j.bmcl.2006.08.026.

Abstract

Structure-guided de novo drug design led to the identification of a novel series of substituted pyridine derivatives as HIF-1alpha prolyl hydroxylase inhibitors. Pyridine carboxyamide derivatives bearing a substituted aryl group at the 5-position of the pyridine ring show appreciable activity, while constraining the side chain by placing a pyrazole carboxylic acid generated a potent lead series with consistent activity against EGLN-1.

MeSH terms

  • Drug Design*
  • Humans
  • Hypoxia-Inducible Factor-Proline Dioxygenases
  • Procollagen-Proline Dioxygenase / antagonists & inhibitors*
  • Pyridines / chemical synthesis*
  • Pyridines / pharmacology*

Substances

  • Pyridines
  • EGLN1 protein, human
  • Procollagen-Proline Dioxygenase
  • Hypoxia-Inducible Factor-Proline Dioxygenases