Recent Progress and Prospects of Small Molecules for NLRP3 Inflammasome Inhibition

被引:34
|
作者
Li, Na [1 ,2 ]
Zhang, Ruijia [1 ,2 ]
Tang, Minghai [1 ,2 ]
Zhao, Min [3 ]
Jiang, Xueqin [1 ,2 ]
Cai, Xiaoying [1 ,2 ]
Ye, Neng [1 ,2 ]
Su, Kaiyue [1 ,2 ]
Peng, Jing [1 ,2 ]
Zhang, Xinlu [1 ,2 ]
Wu, Wenshuang [4 ,5 ]
Ye, Haoyu [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Dept Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Frontiers Sci Ctr Dis Related Mol Network, Lab Metabol & Drug Induced Liver Injury, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, Dept Gen Surg, Div Thyroid Surg, Chengdu 610041, Peoples R China
[5] Sichuan Univ, West China Hosp, Frontiers Sci Ctr Dis Related Mol Network, Lab Thyroid & Parathyroid Dis, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
POTENTIAL TREATMENT; ACTIVATION; IDENTIFICATION; DAPANSUTRILE; PATHOGENESIS; DERIVATIVES; METABOLITE; ANAKINRA; COVID-19; DESIGN;
D O I
10.1021/acs.jmedchem.3c01370
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
NLRP3 inflammasome is a multiprotein complex involved in host immune response-which exerts various biological effects by mediating the maturation and secretion of IL-1 beta and IL-18-and pyroptosis. However, its aberrant activation could cause amplification of inflammatory effects, thereby triggering a range of ailments, including Alzheimer's disease, Parkinson's disease, rheumatoid arthritis, gout, type 2 diabetes mellitus, and cancer. For the past few years, as an attractive anti-inflammatory target, NLRP3-targeting small-molecule inhibitors have been widely reported by both the academic and the industrial communities. In order to deeply understand the advancement of NLRP3 inflammasome inhibitors, we provide comprehensive insights and commentary on drugs currently under clinical investigation, as well as other NLRP3 inflammasome inhibitors from a chemical structure point of view, with an aim to provide new insights for the further development of clinical drugs for NLRP3 inflammasome-mediated diseases.
引用
收藏
页码:14447 / 14473
页数:27
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