Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education), School of Pharmaceutical Sciences, Cheeloo College of Medicine, Shandong University, Jinan 250012, PR China.
Department of Pharmacy, Qilu Hospital of Shandong University, Jinan 250012, PR China.
Bioorg Chem. 2022 Nov;128:106010. doi: 10.1016/j.bioorg.2022.106010. Epub 2022 Jul 9.
As the vital component of innate immune system, the NLRP3 inflammasome is implicated in the onset and progression of a variety of inflammatory diseases and has emerged as an attractive drug target. Herein a series of novel phenyl vinyl sulfone based NLRP3 inflammasome inhibitors were designed, synthesized and biologically characterized. The most potent two hits 7a and 5b showed inhibition on the NLRP3 inflammasome with the IC of 1.83 ± 0.28 µM and 0.91 ± 0.06 µM, respectively. Further characterization confirmed their inhibition of NLRP3-mediated IL-1β release in vivo. Collectively, our findings encourage further research of more potent inhibitors based on this chemical scaffold.
作为先天免疫系统的重要组成部分,NLRP3 炎性小体与多种炎症性疾病的发生和发展有关,已成为有吸引力的药物靶点。本文设计、合成并对一系列基于苯基乙烯砜的新型 NLRP3 炎性小体抑制剂进行了生物学特征分析。两个活性最高的化合物 7a 和 5b 对 NLRP3 炎性小体的抑制作用分别为 IC50 值为 1.83±0.28μM 和 0.91±0.06μM。进一步的表征证实了它们在体内抑制 NLRP3 介导体外 IL-1β 释放的能力。总之,我们的研究结果鼓励进一步研究基于该化学骨架的更有效的抑制剂。