Translating biased agonists from molecules to medications: Serotonin 5-HT


Journal

Pharmacology & therapeutics
ISSN: 1879-016X
Titre abrégé: Pharmacol Ther
Pays: England
ID NLM: 7905840

Informations de publication

Date de publication:
01 2022
Historique:
received: 15 04 2021
revised: 01 06 2021
accepted: 17 06 2021
pubmed: 27 6 2021
medline: 19 3 2022
entrez: 26 6 2021
Statut: ppublish

Résumé

Biased agonism (or "functional selectivity") at G-protein-coupled receptors has attracted rapidly increasing interest as a means to improve discovery of more efficacious and safer pharmacotherapeutics. However, most studies are limited to in vitro tests of cellular signaling and few biased agonists have progressed to in vivo testing. As concerns 5-HT

Identifiants

pubmed: 34174274
pii: S0163-7258(21)00139-X
doi: 10.1016/j.pharmthera.2021.107937
pii:
doi:

Substances chimiques

Serotonin 5-HT1 Receptor Agonists 0
Serotonin Receptor Agonists 0
Receptor, Serotonin, 5-HT1A 112692-38-3
Serotonin 333DO1RDJY

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

107937

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Adrian Newman-Tancredi (A)

Neurolixis, Castres, France. Electronic address: anewmantancredi@neurolixis.com.

Ronan Y Depoortère (RY)

Neurolixis, Castres, France.

Mark S Kleven (MS)

Neurolixis, Castres, France.

Marcin Kołaczkowski (M)

Jagiellonian University, Krakow, Poland.

Luc Zimmer (L)

Université Claude Bernard Lyon1, Lyon, France; Hospices Civils de Lyon, Lyon, France; Lyon Neuroscience Research Center, CNRS-INSERM, France.

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Classifications MeSH