神经保护
渗透剂(生化)
化学
药代动力学
NMDA受体
药理学
缺血
血脑屏障
神经科学
缺血性中风
脑缺血
中枢神经系统
受体
生物化学
医学
心脏病学
心理学
有机化学
作者
Meiling Sun,Lin Wang,Qiaofeng Cao,Xuechun Wang,Ying Zhang,M. Guo,Jie Chen,Yuchen Ma,Le Niu,Yanping Zhang,Mengdie Hu,Mengli Gu,Zhihui Zhu,X. Y. Yao,Junchen Yao,Chen Zhao,Jin Wu,Xiuxiu Liu,Ying‐Mei Lu,Zhen Wang,Qiuping Xiang,Feng Han,Dongsheng Zhu
标识
DOI:10.1021/acs.jmedchem.4c02772
摘要
The death signaling complex comprising extrasynaptic NMDAR and TRPM4 plays a pivotal role in the pathogenesis of ischemic stroke. Targeting the protein-protein interactions between NMDAR and TRPM4 represents a promising therapeutic strategy for ischemic stroke. Herein, we describe the discovery of a novel series of NMDAR/TRPM4 interaction interface inhibitors aimed at enhancing neuroprotective efficacy and optimizing pharmacokinetic profiles. The representative compound
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