Synthesis of 1H-pyridin-2-one derivatives as potent and selective farnesyltransferase inhibitors

Bioorg Med Chem Lett. 2004 Sep 20;14(18):4603-6. doi: 10.1016/j.bmcl.2004.07.004.

Abstract

Two novel series of potent and selective FTase inhibitors have been synthesized using structure-based design. Medicinal chemistry efforts led to the discovery of compound 4e with potent cellular activity and good oral bioavailability in dog. A synthetic route toward novel heterocycles 1,5-dimethyl-6-oxo-4-aryl-1,6-dihydro-pyridine-2-carbonitrile was established. The structure of compound 5c was confirmed by X-ray crystallography.

Publication types

  • Comparative Study

MeSH terms

  • Administration, Oral
  • Alkyl and Aryl Transferases / antagonists & inhibitors*
  • Alkyl and Aryl Transferases / chemistry
  • Animals
  • Crystallography, X-Ray
  • Dogs
  • Farnesyltranstransferase
  • Pyridines / chemical synthesis*
  • Pyridines / chemistry
  • Structure-Activity Relationship

Substances

  • Pyridines
  • Alkyl and Aryl Transferases
  • Farnesyltranstransferase