Development of Novel N-hydroxypyridone Derivatives as Potential Anti-Ischemic Stroke Agents

被引:18
作者
Hu, Linghao [1 ,2 ]
Feng, Hongxuan [3 ,4 ]
Zhang, Hongguang [3 ]
Yu, Songda [5 ]
Zhao, Qinyuan [3 ,4 ]
Wang, Wei [3 ]
Bao, Fengxia [3 ]
Ding, Xun [3 ,4 ]
Hu, Jiajing [2 ]
Wang, Manjiong [1 ,2 ]
Xu, Yixiang [1 ,2 ]
Wu, Zengrui [2 ]
Li, Xiaokang [1 ,2 ]
Tang, Yun [2 ]
Mao, Fei [1 ,2 ]
Chen, Xiaoyan [5 ]
Zhang, Haiyan [3 ,4 ]
Li, Jian [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Sch Pharm, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[5] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
MECHANISMS; ANTIOXIDANT; INHIBITION; DISCOVERY; ISCHEMIA; NXY-059;
D O I
10.1021/acs.jmedchem.9b01338
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Our previous study had identified ciclopirox (CPX) as a promising lead compound for treatment of ischemic stroke. To find better neuroprotective agents, a series of N-hydroxypyridone derivatives based on CPX were designed, synthesized, and evaluated in this study. Among these derivatives, compound 11 exhibits significant neuroprotection against oxygen glucose deprivation and oxidative stress -induced injuries in neuronal cells. Moreover, compound 11 possesses good blood-brain barrier permeability and superior antioxidant capability. In addition, a complex of compound 11 with olamine-11.01a possesses good water solubility, negligible hERG inhibition, and superior metabolic stability. The in vivo experiment demonstrates that 11.01a significantly reduces brain infarction and alleviates neurological deficits in middle cerebral artery occlusion rats. Hence, compound 11.01a is identified in our research as a prospective prototype in the innovation of stroke treatment.
引用
收藏
页码:1051 / 1067
页数:17
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