Synthesis of 3-ureido derivatives of coumarin and 2-quinolone as potent acyl-CoA: cholesterol acyltransferase inhibitors

Chem Pharm Bull (Tokyo). 1995 Apr;43(4):616-25. doi: 10.1248/cpb.43.616.

Abstract

Novel 3-ureido derivatives of 4-phenylcoumarin and 4-phenyl-2-quinolone were synthesized and evaluated for acyl-CoA: cholesterol acyltransferase (ACAT)-inhibitory activity. These derivatives inhibited rat intestinal ACAT with IC50 values at the 10(-8) to 10(-9) M level and were found to normalize plasma cholesterol levels in cholesterol-fed rats when administered as dietary admixtures.

MeSH terms

  • Animals
  • Coumarins / chemical synthesis*
  • Coumarins / chemistry
  • Coumarins / pharmacology
  • Hypolipidemic Agents / pharmacology
  • In Vitro Techniques
  • Magnetic Resonance Spectroscopy
  • Male
  • Quinolones / chemical synthesis*
  • Quinolones / chemistry
  • Quinolones / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Sterol O-Acyltransferase / antagonists & inhibitors*

Substances

  • 4-phenylquinolone
  • Coumarins
  • Hypolipidemic Agents
  • Quinolones
  • 4-phenylcoumarin
  • Sterol O-Acyltransferase