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The progress of small molecules against cannabinoid 2 receptor (CB2R).
Zhang, Qinying; Zhao, Ying; Wu, Jianan; Zhong, Wanting; Huang, Wenhai; Pan, Youlu.
Afiliação
  • Zhang Q; Hangzhou Medical College, Hangzhou, Zhejiang, China.
  • Zhao Y; Hangzhou Medical College, Hangzhou, Zhejiang, China.
  • Wu J; Hangzhou Medical College, Hangzhou, Zhejiang, China.
  • Zhong W; Hangzhou Medical College, Hangzhou, Zhejiang, China.
  • Huang W; Hangzhou Medical College, Hangzhou, Zhejiang, China. Electronic address: hwh@hmc.edu.cn.
  • Pan Y; Hangzhou Medical College, Hangzhou, Zhejiang, China. Electronic address: panyl@hmc.edu.cn.
Bioorg Chem ; 144: 107075, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38218067
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canabinoides / Inflamação Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canabinoides / Inflamação Idioma: En Ano de publicação: 2024 Tipo de documento: Article