Novel benzothiophene H1-antihistamines for the treatment of insomnia

Bioorg Med Chem Lett. 2010 Apr 1;20(7):2316-20. doi: 10.1016/j.bmcl.2010.01.134. Epub 2010 Feb 2.

Abstract

SAR of lead benzothiophene H(1)-antihistamine 2 was explored to identify backup candidates with suitable pharmacokinetic profiles for an insomnia program. Several potent and selective H(1)-antihistamines with a range of projected half-lives in humans were identified. Compound 16d had a suitable human half-life as demonstrated in a human microdose study, but variability in pharmacokinetic profile, attributed to metabolic clearance, prevented further development of this compound. Compound 28b demonstrated lower predicted clearance in preclinical studies, and may represent a more suitable backup compound.

MeSH terms

  • Histamine H1 Antagonists / chemistry
  • Histamine H1 Antagonists / pharmacokinetics*
  • Histamine H1 Antagonists / pharmacology*
  • Histamine H1 Antagonists / therapeutic use
  • Humans
  • Receptors, Histamine H1 / metabolism
  • Sleep Initiation and Maintenance Disorders / drug therapy*
  • Structure-Activity Relationship
  • Thiophenes / chemistry
  • Thiophenes / pharmacokinetics*
  • Thiophenes / pharmacology*
  • Thiophenes / therapeutic use

Substances

  • Histamine H1 Antagonists
  • Receptors, Histamine H1
  • Thiophenes
  • benzothiophene