Recent Advances on Type-2 Cannabinoid (CB 2 ) Receptor Agonists and their Therapeutic Potential.

Autor: Gasperi V; Department of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy., Guzzo T; C4T S.r.l Colosseum Combinatorial Chemistry Centre for Technology, Rome, Italy., Topai A; C4T S.r.l Colosseum Combinatorial Chemistry Centre for Technology, Rome, Italy., Gambacorta N; Department of Pharmacy-Pharmaceutical Sciences, University of Bari, Bari, Italy., Ciriaco F; Department of Chemistry, University of Bari, Bari, Italy., Nicolotti O; Department of Pharmacy-Pharmaceutical Sciences, University of Bari, Bari, Italy., Maccarrone M; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.; European Center for Brain Research/Santa Lucia Foundation IRCCS, Rome, Italy.
Jazyk: angličtina
Zdroj: Current medicinal chemistry [Curr Med Chem] 2023; Vol. 30 (12), pp. 1420-1457.
DOI: 10.2174/0929867329666220825161603
Abstrakt: In the last decade, selective modulators of type-2 cannabinoid receptor (CB 2 ) have become a major focus to target endocannabinoid signaling in humans. Indeed, heterogeneously expressed within our body, CB 2 actively regulates several physio-pathological processes, thus representing a promising target for developing specific and safe therapeutic drugs. If CB 2 modulation has been extensively studied since the very beginning for the treatment of pain and inflammation, the more recent involvement of this receptor in other pathological conditions has further strengthened the pursuit of novel CB 2 agonists in the last five years. Against this background, here we discuss the most recent evidence of the protective effects of CB 2 against pathological conditions, emphasizing central nervous system disorders, bone and synovial diseases, and cancer. We also summarize the most recent advances in the development of CB 2 agonists, focusing on the correlation between different chemical classes and diverse therapeutic applications. Data mining includes a review of the CB 2 ligands disclosed in patents also released in the last five years. Finally, we discuss how the recent elucidation of CB 2 tertiary structure has provided new details for the rational design of novel and more selective CB 2 agonists, thus supporting innovative strategies to develop effective therapeutics. Our overview of the current knowledge on CB 2 agonists provides pivotal information on the structure and function of different classes of molecules and opens possible avenues for future research.
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Databáze: MEDLINE