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Current Medicinal Chemistry


ISSN (Print): 0929-8673
ISSN (Online): 1875-533X

General Review Article

Recent Advances on Type-2 Cannabinoid (CB2) Receptor Agonists and their Therapeutic Potential

Author(s): Valeria Gasperi*, Tatiana Guzzo*, Alessandra Topai, Nicola Gambacorta, Fulvio Ciriaco, Orazio Nicolotti and Mauro Maccarrone

Volume 30, Issue 12, 2023

Published on: 27 October, 2022

Page: [1420 - 1457] Pages: 38

DOI: 10.2174/0929867329666220825161603

Price: $65


In the last decade, selective modulators of type-2 cannabinoid receptor (CB2) have become a major focus to target endocannabinoid signaling in humans. Indeed, heterogeneously expressed within our body, CB2 actively regulates several physio-pathological processes, thus representing a promising target for developing specific and safe therapeutic drugs. If CB2 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 CB2 agonists in the last five years.

Against this background, here we discuss the most recent evidence of the protective effects of CB2 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 CB2 agonists, focusing on the correlation between different chemical classes and diverse therapeutic applications. Data mining includes a review of the CB2 ligands disclosed in patents also released in the last five years. Finally, we discuss how the recent elucidation of CB2 tertiary structure has provided new details for the rational design of novel and more selective CB2 agonists, thus supporting innovative strategies to develop effective therapeutics.

Our overview of the current knowledge on CB2 agonists provides pivotal information on the structure and function of different classes of molecules and opens possible avenues for future research.

Keywords: Biased signaling, drug design, endocannabinoid, human disease, signal transduction, therapy, type-2 cannabinoid receptor.

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