Discovery of Soluble Epoxide Hydrolase Inhibitors from Chemical Synthesis and Natural Products

被引:70
|
作者
Sun, Cheng-Peng [1 ]
Zhang, Xin-Yue [1 ]
Morisseau, Christophe [2 ]
Hwang, Sung Hee [2 ]
Zhang, Zhan-Jun [3 ]
Hammock, Bruce D. [2 ]
Ma, Xiao-Chi [1 ,4 ]
机构
[1] Dalian Med Univ, Coll Pharm, Coll Inst Integrat Med, Dalian Key Lab Metab Target Characterizat & Tradi, Dalian 116044, Peoples R China
[2] Univ Calif Davis, UC Davis Comprehens Canc Ctr, Dept Entomol & Nematol, Davis, CA 95616 USA
[3] Beijing Normal Univ, State Key Lab Cognit Neurosci & Learning, Beijing 100875, Peoples R China
[4] Hangzhou Normal Univ, Coll Pharm, Sch Med, Hangzhou 311121, Peoples R China
基金
中国国家自然科学基金;
关键词
AMIDE-BASED INHIBITORS; ENCODED LIBRARY TECHNOLOGY; NON-UREA INHIBITORS; EPOXYEICOSATRIENOIC ACIDS; ARACHIDONIC-ACID; 11,12-EPOXYEICOSATRIENOIC ACID; CIMICIFUGA-DAHURICA; ALZHEIMERS-DISEASE; THERAPEUTIC TARGET; BLOOD-PRESSURE;
D O I
10.1021/acs.jmedchem.0c01507
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Soluble epoxide hydrolase (sEH) is an alpha/beta hydrolase fold protein and widely distributed in numerous organs including the liver, kidney, and brain. The inhibition of sEH can effectively maintain endogenous epoxyeicosatrienoic acids (EETs) levels and reduce dihydroxyeicosatrienoic acids (DHETs) levels, resulting in therapeutic potentials for cardiovascular, central nervous system, and metabolic diseases. Therefore, since the beginning of this century, the development of sEH inhibitors is a hot research topic. A variety of potent sEH inhibitors have been developed by chemical synthesis or isolated from natural sources. In this review, we mainly summarized the interconnected aspects of sEH with cardiovascular, central nervous system, and metabolic diseases and then focus on representative inhibitors, which would provide some useful guidance for the future development of potential sEH inhibitors.
引用
收藏
页码:184 / 215
页数:32
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