Synthesis and biological activity of 2-alkylbenzimidazoles bearing a N-phenylpyrrole moiety as novel angiotensin II AT1 receptor antagonists

Bioorg Med Chem Lett. 2007 May 15;17(10):2921-6. doi: 10.1016/j.bmcl.2007.02.042. Epub 2007 Feb 20.

Abstract

A series of 2-alkylbenzimidazoles bearing a N-phenylpyrrole moiety were synthesized and evaluated as a novel class of AT(1) receptor antagonists. Among them, compounds 10a and 10g inhibited [(125)I] AngII-binding affinity to AT(1) receptor at nanomolar level and potently inhibited the Ang II-induced pressor response by oral administration. Moreover, evaluation in spontaneously hypertensive rats showed that 10a is an orally active AT(1) receptor antagonist.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Angiotensin II Type 1 Receptor Blockers / chemical synthesis*
  • Angiotensin II Type 1 Receptor Blockers / pharmacology*
  • Animals
  • Models, Molecular
  • Molecular Structure
  • Rats
  • Rats, Inbred SHR
  • Structure-Activity Relationship

Substances

  • Angiotensin II Type 1 Receptor Blockers