Novel analogues of bradykinin conformationally restricted in the C-terminal part of the molecule

✍ Scribed by Małgorzata Śleszyńska; Tomasz H. Wierzba; Krzysztof Malinowski; Lenka Borovičková; Izabela Małuch; Dariusz Sobolewski; Bernard Lammek; Jiřina Slaninová; Adam Prahl

• Book ID: 105359978
• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 138 KB
• Volume: 17
• Category: Article
• ISSN: 1075-2617
• DOI: 10.1002/psc.1351

✦ Synopsis

Abstract

In the present work, achiral non‐coded amino acids, N‐(Bzl)‐Gly, X~1~ or X~2~, were substituted at position 7 of the model B~2~ receptor antagonist [D‐Arg^0^, Hyp^3^, Thi^5, 8^, D‐Phe^7^]‐BK. The N‐terminal amino group of the analogues was either free or acylated with 1‐Aca or Aaa. Biological activity of the compounds was assessed in the in vitro rat uterus test and the in vivo rat blood pressure test. The X~1~^7^ substitution resulted in a decrease in antagonistic potency of the new peptide in both assays. The X~2~^7^ and N‐(Bzl)‐Gly^7^ substituted analogues showed weak agonistic properties in the rat uterus test. Interestingly, the latter compound exhibited dual activity in the pressor test, i.e. intrinsic vasodepressor action and at the same time a weak antagonistic effect. Acylation of the N‐terminus enhanced antagonistic properties of the resulting peptides in the rat blood pressure test in the case of compounds containing X~1~ or X~2~ modification. Our studies provide new information about structure–activity relationship of the BK antagonists which may be helpful for designing more potent B~2~ receptor blockers. Copyright © 2011 European Peptide Society and John Wiley & Sons, Ltd.