炎症体
化学
上睑下垂
体内
感染性休克
药理学
脂多糖
生物化学
免疫学
败血症
医学
受体
生物
生物技术
作者
Zhiyuan Fu,Yangqin Duan,Heying Pei,Yurong Zou,Minghai Tang,Yong Chen,Tao Yang,Ziyan Ma,Wei Yan,Kaiyue Su,Xiaoying Cai,Tao Guo,Yaxin Teng,Tao Jia,Lijuan Chen
标识
DOI:10.1021/acs.jmedchem.4c01341
摘要
The NLRP3 inflammasome is a multiprotein complex that is a component of the innate immune system, involved in the production of pro-inflammatory cytokines. Its abnormal activation is associated with many inflammatory diseases. In this study, we designed and synthesized a series of NLRP3 inflammasome inhibitors based on pyridazine scaffolds. Among them, P33 exhibited significant inhibitory effects against nigericin-induced IL-1β release in THP-1 cells, BMDMs, and PBMCs, with IC50 values of 2.7, 15.3, and 2.9 nM, respectively. Mechanism studies indicated that P33 directly binds to NLRP3 protein (KD = 17.5 nM), inhibiting NLRP3 inflammasome activation and pyroptosis by suppressing ASC oligomerization during NLRP3 assembly. Additionally, P33 displayed excellent pharmacokinetic properties, with an oral bioavailability of 62%. In vivo efficacy studies revealed that P33 significantly ameliorated LPS-induced septic shock and MSU crystal-induced peritonitis in mice. These results indicate that P33 has great potential for further development as a candidate for treating NLRP3 inflammasome-mediated diseases.
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