渗透剂(生化)
化学
药代动力学
药理学
血脑屏障
神经科学
中枢神经系统
医学
生物
有机化学
作者
Meiling Sun,Lin Wang,Qiaofeng Cao,Xuechun Wang,Ying Zhang,Manyu 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
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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