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Progress on the development of Class A GPCR‐biased ligands.

Authors :
Morales, Paula
Scharf, Magdalena M.
Bermudez, Marcel
Egyed, Attila
Franco, Rafael
Hansen, Olivia K.
Jagerovic, Nadine
Jakubík, Jan
Keserű, György M.
Kiss, Dóra Judit
Kozielewicz, Pawel
Larsen, Olav
Majellaro, Maria
Mallo‐Abreu, Ana
Navarro, Gemma
Prieto‐Díaz, Rubén
Rosenkilde, Mette M.
Sotelo, Eddy
Stark, Holger
Werner, Tobias
Source :
British Journal of Pharmacology. Sep2024, p1. 52p. 108 Illustrations.
Publication Year :
2024

Abstract

Class A G protein‐coupled receptors (GPCRs) continue to garner interest for their essential roles in cell signalling and their importance as drug targets. Although numerous drugs in the clinic target these receptors, over 60% GPCRs remain unexploited. Moreover, the adverse effects triggered by the available unbiased GPCR modulators, limit their use and therapeutic value. In this context, the elucidation of biased signalling has opened up new pharmacological avenues holding promise for safer therapeutics. Functionally selective ligands favour receptor conformations facilitating the recruitment of specific effectors and the modulation of the associated pathways. This review surveys the current drug discovery landscape of GPCR‐biased modulators with a focus on recent advances. Understanding the biological effects of this preferential coupling is at different stages depending on the Class A GPCR family. Therefore, with a focus on individual GPCR families, we present a compilation of the functionally selective modulators reported over the past few years. In doing so, we dissect their therapeutic relevance, molecular determinants and potential clinical applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00071188
Database :
Academic Search Index
Journal :
British Journal of Pharmacology
Publication Type :
Academic Journal
Accession number :
179588722
Full Text :
https://doi.org/10.1111/bph.17301