4.7 Article

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

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 64, Issue 1, Pages 184-215

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.0c01507

Keywords

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Funding

  1. National Natural Science Foundation of China [81930112, 81703769]
  2. National Key Research and Development Program of China [2018YFC1705900]
  3. Liaoning Provincial Key Research and Development Program [2019JH2/10300022]
  4. Dalian High Level Talents Innovation Support Plan [2019RD15]
  5. Revolutionizing Innovative, Visionary Environmental Health Research Program of the National Institute of Environmental Health Sciences [R35 ES030443]
  6. Superfund Basic Research Program of the National Institutes of Environmental Health Sciences [P42 ES04699]
  7. Liaoning Revitalization Talents Program
  8. Natural Science Foundation of Liaoning Province [2020-MS-256]
  9. Dalian Young Star of Science and Technology [2019RQ123]

Ask authors/readers for more resources

Soluble epoxide hydrolase (sEH) is a vital protein that plays a crucial role in cardiovascular, central nervous system, and metabolic diseases. Inhibiting sEH may offer potential solutions for the treatment of these diseases.
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.

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