A new class of 5-HT2B antagonists possesses favorable potency, selectivity, and rat pharmacokinetic properties

Bioorg Med Chem Lett. 2009 Apr 15;19(8):2206-10. doi: 10.1016/j.bmcl.2009.02.126. Epub 2009 Mar 9.

Abstract

We have been exploring the potential of 5-HT(2B) antagonists as a therapy for chronic heart failure. To assess the potential of this therapeutic approach, we sought compounds possessing the following attributes: (a) potent and selective antagonism of the 5-HT(2B) receptor, (b) low impact of serum proteins on potency, and (c) desirable pharmacokinetic properties. This Letter describes our investigation of a biphenyl benzimidazole class of compounds that resulted in 5-HT(2B) antagonists possessing the above attributes. Improving potency in a human serum albumin shift assay proved to be the most significant SAR discovery.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Binding Sites
  • Male
  • Quantitative Structure-Activity Relationship
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Receptor, Serotonin, 5-HT2B / chemistry
  • Receptor, Serotonin, 5-HT2B / metabolism*
  • Serotonin 5-HT2 Receptor Antagonists*
  • Serotonin Antagonists / chemistry*
  • Serotonin Antagonists / classification
  • Serotonin Antagonists / pharmacokinetics*

Substances

  • Receptor, Serotonin, 5-HT2B
  • Serotonin 5-HT2 Receptor Antagonists
  • Serotonin Antagonists