Synthesis of a new class of druglike angiotensin II C-terminal mimics with affinity for the AT2 receptor

J Med Chem. 2007 Apr 5;50(7):1711-5. doi: 10.1021/jm0613469. Epub 2007 Mar 15.

Abstract

Four tripeptides corresponding to the C-terminal region of angiotensin II were synthesized. One of these peptides (Ac-His-Pro-Ile) showed moderate binding affinity for the AT2 receptor. Two aromatic histidine-related scaffolds were synthesized and introduced in the tripeptides to give eight new peptidomimetic structures. Three of the new peptide-derived druglike molecules exhibited selective, nanomolar affinity for the AT2 receptor. These ligands may become lead compounds in the future development of novel classes of selective AT2 receptor agonists.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II / chemistry*
  • Animals
  • Female
  • In Vitro Techniques
  • Ligands
  • Liver / metabolism
  • Models, Molecular
  • Molecular Mimicry
  • Myometrium / metabolism
  • Oligopeptides / chemical synthesis*
  • Oligopeptides / chemistry
  • Oligopeptides / pharmacology
  • Radioligand Assay
  • Rats
  • Receptor, Angiotensin, Type 2 / agonists*
  • Structure-Activity Relationship
  • Swine

Substances

  • Ligands
  • Oligopeptides
  • Receptor, Angiotensin, Type 2
  • Angiotensin II