The progress of small molecules against cannabinoid 2 receptor (CB2R)

被引:3
|
作者
Zhang, Qinying [1 ]
Zhao, Ying [1 ]
Wu, Jianan [1 ]
Zhong, Wanting [1 ]
Huang, Wenhai [1 ]
Pan, Youlu [1 ]
机构
[1] Hangzhou Med Coll, Hangzhou, Zhejiang, Peoples R China
关键词
CB; 2; R; Endogenous ligands; Natural compounds; Small molecules; NOLADIN ETHER ACTS; BINDING-AFFINITY; ENDOCANNABINOID SYSTEM; SELECTIVE LIGANDS; CB1; RECEPTORS; IN-VITRO; AGONISTS; DISCOVERY; POTENT; DERIVATIVES;
D O I
10.1016/j.bioorg.2023.107075
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The two subtypes of cannabinoid receptors (CBR), namely CB1R and CB2R, belong to the G protein-coupled receptor (GPCR) superfamily and are confirmed as potential therapeutic targets for a variety of diseases such as inflammation, neuropathic pain, and immune-related disorders. Since CB1R is mainly distributed in the central nervous system (CNS), it could produce severe psychiatric adverse reactions and addiction. In contrast, CB2R are predominantly distributed in the peripheral immune system with minimal CNS-related side effects. Therefore, more attention has been devoted to the discovery of CB2R ligands. In view of the favorable profile of CB2R, many high-binding affinity and selectivity CB2R ligands have been developed recently. This paper reviews recent research progress on CB2R ligands, including endogenous CB2R ligands, natural compounds, and novel small molecules, in order to provide a reference for subsequent CB2R ligand development.
引用
收藏
页数:39
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