炎症体
化学
体内
体外
砜
先天免疫系统
药理学
组合化学
生物化学
生物
有机化学
受体
生物技术
作者
Xiangna Zhang,Ana Xu,Yingying Ran,Chao Wei,Fei Xie,Jingde Wu
标识
DOI:10.1016/j.bioorg.2022.106010
摘要
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 IC50 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.
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