Substituted oxazolidinones as novel NPC1L1 ligands for the inhibition of cholesterol absorption

Bioorg Med Chem Lett. 2008 Jan 15;18(2):546-53. doi: 10.1016/j.bmcl.2007.11.083. Epub 2007 Nov 28.

Abstract

Cholesterol absorption inhibition (CAI) represents an important treatment option for hypercholesterolemia. Herein, we report the design and evaluation of a series of substituted oxazolidinones as ligands for the Niemann Pick C1 Like 1 (NPC1L1) protein, a key mediator of cholesterol transport. Novel analogs were initially evaluated in a brush border membrane NPC1L1 binding assay; subsequently, promising compounds were evaluated in vivo for acute inhibition of cholesterol absorption. These studies identified analogs with low micromolar NPC1L1 binding affinity and acute in vivo efficacy of >50% absorption inhibition at 3mg/kg.

MeSH terms

  • Animals
  • Cholesterol / metabolism*
  • Intestinal Absorption / drug effects*
  • Ligands
  • Membrane Transport Proteins / metabolism*
  • Microvilli / metabolism
  • Oxazolidinones / chemistry
  • Oxazolidinones / metabolism
  • Oxazolidinones / pharmacokinetics
  • Oxazolidinones / pharmacology*
  • Rats
  • X-Ray Diffraction

Substances

  • Ligands
  • Membrane Transport Proteins
  • NPC1L1 protein, rat
  • Oxazolidinones
  • Cholesterol