Developing the Cannabinoid Receptor 2 (CB2) pharmacopoeia: past, present, and future.


Journal

Trends in pharmacological sciences
ISSN: 1873-3735
Titre abrégé: Trends Pharmacol Sci
Pays: England
ID NLM: 7906158

Informations de publication

Date de publication:
09 2022
Historique:
received: 02 02 2022
revised: 23 06 2022
accepted: 27 06 2022
pubmed: 30 7 2022
medline: 17 8 2022
entrez: 29 7 2022
Statut: ppublish

Résumé

Cannabinoid Receptor 2 (CB2) is a G protein-coupled receptor (GPCR) with considerable, though as yet unrealised, therapeutic potential. Promising preclinical data supports the applicability of CB2 activation in autoimmune and inflammatory diseases, pain, neurodegeneration, and osteoporosis. A diverse pharmacopoeia of cannabinoid ligands is available, which has led to considerable advancements in the understanding of CB2 function and extensive preclinical evaluation. However, until recently, most CB2 ligands were highly lipophilic and as such not optimal for clinical application due to unfavourable physicochemical properties. A number of strategies have been applied to develop CB2 ligands to achieve closer to 'drug-like' properties and a few such compounds have now undergone clinical trial. We review the current state of CB2 ligand development and progress in optimising physicochemical properties, understanding advanced molecular pharmacology such as functional selectivity, and clinical evaluation of CB2-targeting compounds.

Identifiants

pubmed: 35906103
pii: S0165-6147(22)00137-7
doi: 10.1016/j.tips.2022.06.010
pii:
doi:

Substances chimiques

Cannabinoids 0
Ligands 0
Receptor, Cannabinoid, CB1 0
Receptors, Cannabinoid 0
Receptors, G-Protein-Coupled 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

754-771

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

Zak M Whiting (ZM)

Department of Pharmacology and Clinical Pharmacology, School of Medical Sciences, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand; Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.

Jiazhen Yin (J)

Department of Chemistry, Division of Sciences, University of Otago, Dunedin, New Zealand.

Sara M de la Harpe (SM)

Department of Chemistry, Division of Sciences, University of Otago, Dunedin, New Zealand.

Andrea J Vernall (AJ)

Department of Chemistry, Division of Sciences, University of Otago, Dunedin, New Zealand; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand.

Natasha L Grimsey (NL)

Department of Pharmacology and Clinical Pharmacology, School of Medical Sciences, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand; Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand; Maurice Wilkins Centre for Molecular Biodiscovery, Auckland, New Zealand. Electronic address: n.grimsey@auckland.ac.nz.

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Classifications MeSH