Transient receptor potential ankyrin 1 (TRPA1) modulators: Recent update and future perspective

被引:12
|
作者
Hu, Zelin [1 ,2 ,3 ,4 ]
Zhang, Ya [1 ,2 ,3 ,4 ]
Yu, Wenhan [5 ]
Li, Junjie [1 ,2 ,3 ]
Yao, Jiaqi [1 ,2 ,3 ,4 ]
Zhang, Jifa [1 ,2 ,3 ]
Wang, Jiaxing [6 ]
Wang, Chengdi [1 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Resp Hlth, Frontiers Sci Ctr Dis Related Mol Network,Dept Pul, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Precis Med Key Lab Sichuan Prov, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Precis Med Res Ctr, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Univ, Coll Life Sci, Chengdu 610064, Peoples R China
[5] Univ Calif Berkeley, Coll Letters & Sci, Berkeley, CA 94720 USA
[6] Univ Tennessee Hlth Sci Ctr, Coll Pharm, Dept Pharmaceut Sci, Memphis, TN 38163 USA
关键词
TRPA1; Antagonists; Agonists; Ion channel; SENSITIVE AMINE OXIDASES; ION-CHANNEL TRPA1; NF-KAPPA-B; IN-VIVO; NEUROGENIC INFLAMMATION; BIOLOGICAL EVALUATION; MARINE SPONGE; ACTIVATION; LIGUSTILIDE; PAIN;
D O I
10.1016/j.ejmech.2023.115392
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The transient receptor potential ankyrin 1 (TRPA1) channel is a non-selective cation channel that senses irritant chemicals. Its activation is closely associated with pain, inflammation, and pruritus. TRPA1 antagonists are promising treatments for these diseases, and there has been a recent upsurge in their application to new areas such as cancer, asthma, and Alzheimer's disease. However, due to the generally disappointing performance of TRPA1 antagonists in clinical studies, scientists must pursue the development of antagonists with higher selectivity, metabolic stability, and solubility. Moreover, TRPA1 agonists provide a deeper understanding of activation mechanisms and aid in antagonist screening. Therefore, we summarize the TRPA1 antagonists and agonists developed in recent years, with a particular focus on structure-activity relationships (SARs) and phar-macological activity. In this perspective, we endeavor to keep abreast of cutting-edge ideas and provide inspi-ration for the development of more effective TRPA1-modulating drugs.
引用
收藏
页数:19
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