ACAT inhibitors derived from hetero-Diels-Alder cycloadducts of thioaldehydes

Bioorg Med Chem. 1996 Sep;4(9):1493-513. doi: 10.1016/0968-0896(96)00143-5.

Abstract

Acyl-CoA:cholesterol acyltransferase (ACAT) is the enzyme largely responsible for intracellular cholesterol esterification. A systemic inhibitor of ACAT is believed to be able to slow or even reverse the atherosclerotic process. Towards that goal, a series of cyclic sulfides, derived from the hetero-Diels-Alder reaction of thioaldehydes with 1,3-dienes, and bearing carboxamide substituents, were prepared and evaluated for in vitro (in several tissues and species) and ex vivo ACAT inhibition. Minor changes in subsequent structure were found to have a significant effect in optimization of the biological activity of this series of compounds.

MeSH terms

  • Aldehydes / chemistry*
  • Animals
  • Chemical Phenomena
  • Chemistry
  • Chromatography, High Pressure Liquid
  • Enzyme Inhibitors / chemistry*
  • Male
  • Microsomes, Liver / enzymology
  • Rats
  • Rats, Sprague-Dawley
  • Sterol O-Acyltransferase / antagonists & inhibitors*
  • Sulfhydryl Compounds / chemistry*

Substances

  • Aldehydes
  • Enzyme Inhibitors
  • Sulfhydryl Compounds
  • Sterol O-Acyltransferase