Bradykinin receptors in GtoPdb v.2023.1

Authors

  • Joseph Coulson University of Edinburgh
  • Réjean Couture Université de Montréal
  • Alexander Faussner Ludwig-Maximilians-Universität
  • Fernand Gobeil Jr Université de Sherbrooke
  • Fredrik Leeb-Lundberg Lunds Universitet
  • Francois Marceau Université Laval
  • Werner Muller-Esterl Johann Wolfgang Goethe-University
  • Doug Pettibone Merck Research Laboratories
  • Bruce Zuraw University of California San Diego

DOI:

https://doi.org/10.2218/gtopdb/F10/2023.1

Abstract

Bradykinin (or kinin) receptors (nomenclature as agreed by the NC-IUPHAR subcommittee on Bradykinin (kinin) Receptors [92]) are activated by the endogenous peptides bradykinin (BK), [des-Arg9]bradykinin, Lys-BK (kallidin), [des-Arg10]kallidin, [Phospho-Ser6]-Bradykinin, T-kinin (Ile-Ser-BK), [Hyp3]bradykinin and Lys-[Hyp3]-bradykinin. Variation in pharmacology and activity of B1 and B2 receptor antagonists at species orthologs has been documented. icatibant (Hoe140, Firazir) is approved in North America and Europe for the treatment of acute attacks of hereditary angioedema. Inhibition of bradykinin with icatibant in COVID-19 infection is under clinical evaluation, with trial NCT05407597 expected to complete in mid 2023.

Published

26-Apr-2023

How to Cite

Coulson, J. (2023) “Bradykinin receptors in GtoPdb v.2023.1”, IUPHAR/BPS Guide to Pharmacology CITE, 2023(1). doi: 10.2218/gtopdb/F10/2023.1.

Issue

Section

Summaries