7-(Disubstituted thiazolyl)-3,5-dihydroxy-6-heptenoic/heptanoic acid derivatives as HMG-CoA reductase inhibitors

Bioorg Med Chem. 1994 Aug;2(8):799-806. doi: 10.1016/s0968-0896(00)82180-x.

Abstract

A series of disubstituted thiazoles, functionalized with the essential 3,5-dihydroxy-6-heptenoic or heptanoic chain, were prepared and evaluated for their ability to inhibit the enzyme HMG-CoA reductase in vitro. All the synthesized compounds 46-61 showed a moderate inhibitory potency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors*
  • In Vitro Techniques
  • Liver / enzymology
  • Molecular Structure
  • Rats
  • Structure-Activity Relationship
  • Thiazoles / chemical synthesis
  • Thiazoles / chemistry
  • Thiazoles / pharmacology*

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Thiazoles