Chromanol derivatives--a novel class of CETP inhibitors

Bioorg Med Chem Lett. 2011 Jan 1;21(1):488-91. doi: 10.1016/j.bmcl.2010.10.110. Epub 2010 Oct 26.

Abstract

Based on our former development candidate BAY 38-1315, optimization efforts led to the discovery of a novel chemical class of orally active cholesteryl ester transfer protein (CETP) inhibitors. The chromanol derivative 19b is a highly potent CETP inhibitor with favorable pharmacokinetic properties suitable for clinical studies. Chemical process optimization furnished a robust synthesis for a kilogram-scale process.

MeSH terms

  • Administration, Oral
  • Animals
  • Benzopyrans / chemical synthesis
  • Benzopyrans / chemistry*
  • Benzopyrans / pharmacokinetics
  • Cholesterol Ester Transfer Proteins / antagonists & inhibitors*
  • Cholesterol Ester Transfer Proteins / metabolism
  • Cholesterol, HDL / metabolism
  • Chromans / chemical synthesis
  • Chromans / chemistry*
  • Chromans / pharmacokinetics
  • Dogs
  • Humans
  • Mice
  • Mice, Transgenic
  • Rats
  • Spiro Compounds / chemical synthesis
  • Spiro Compounds / chemistry*
  • Spiro Compounds / pharmacokinetics
  • Structure-Activity Relationship

Substances

  • Benzopyrans
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Chromans
  • Spiro Compounds
  • 2,2,5,7,8-pentamethyl-1-hydroxychroman