Inhibition of vertebrate squalene epoxidase by isoprenyl gallates and phenylalkyl gallates

Bioorg Med Chem Lett. 2000 Nov 20;10(22):2525-8. doi: 10.1016/s0960-894x(00)00526-6.

Abstract

Galloy esters with 'substrate-like' isoprenoid or phenylalkyl side chains were newly synthesized and tested for the enzyme inhibition activities toward recombinant rat squalene epoxidase. Isoprenyl gallates (4-6) showed good inhibition (IC50 = 1.5 5.1 microM), as potent as previously reported substrate analogues, while phenylalkyl gallates (7-10) were moderate inhibitors of the enzyme (IC50 = 12-61 microM).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Gallic Acid / analogs & derivatives
  • Gallic Acid / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry / methods
  • Oxygenases / antagonists & inhibitors*
  • Rats
  • Squalene Monooxygenase

Substances

  • Enzyme Inhibitors
  • Gallic Acid
  • Oxygenases
  • Squalene Monooxygenase