Discovery and optimization of 2-phenyloxazole derivatives as diacylglycerol acyltransferase-1 inhibitors

Bioorg Med Chem Lett. 2011 Dec 1;21(23):7205-9. doi: 10.1016/j.bmcl.2011.09.039. Epub 2011 Sep 22.

Abstract

In a discovery effort to find safe and effective DGAT-1 inhibitors, we have identified 2-phenyloxazole 4-carboxamide 1 as a conformationally constrained analog of a hydrazide hit, which was previously identified from high-throughput screening. Further optimization of this series has led to chemically more stable 2-phenyloxazole-based DGAT-1 inhibitor 25 with improved solubility, cell-based activity, and pharmacokinetic properties. Compound 25 also demonstrated in vivo efficacy in a diet-induced obesity (DIO) rat model.

MeSH terms

  • Administration, Oral
  • Animals
  • Body Weight
  • Diacylglycerol O-Acyltransferase / antagonists & inhibitors*
  • Diacylglycerol O-Acyltransferase / chemistry
  • Disease Models, Animal
  • Drug Discovery*
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors* / chemistry
  • Enzyme Inhibitors* / pharmacology
  • Enzyme Inhibitors* / therapeutic use
  • Humans
  • Inhibitory Concentration 50
  • Mice
  • Molecular Structure
  • Obesity / drug therapy
  • Oxazoles / chemistry*
  • Oxazoles / pharmacology*
  • Oxazoles / therapeutic use
  • Rats
  • Solubility
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • Oxazoles
  • Diacylglycerol O-Acyltransferase