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PMID: 15822179 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Epoxide hydrolases: mechanisms, inhibitor designs, and biological roles.

Annual review of pharmacology and toxicology ·Vol. 45 ·2005-00-00 ·Pages 311-33

Morisseau C, Hammock BD

Abstract

Organisms are exposed to epoxide-containing compounds from both exogenous and endogenous sources. In mammals, the hydration of these compounds by various epoxide hydrolases (EHs) can not only regulate their genotoxicity but also, for lipid-derived epoxides, their endogenous roles as chemical mediators. Recent findings suggest that the EHs as a family represent novel drug discovery targets for regulation of blood pressure, inflammation, cancer progression, and the onset of several other diseases. Knowledge of the EH mechanism provides a solid foundation for the rational design of inhibitors, and this review summarizes the current understanding of the catalytic mechanism of the EHs. Although the overall EH mechanism is now known, the molecular basis of substrate selectivity, possible allosteric regulation, and many fine details of the catalytic mechanism remain to be solved. Finally, recent development in the design of EH inhibitors and the EH biological role are discussed.

MeSH Terms
Animals Drug Design Epoxide Hydrolases/antagonists & inhibitors,chemistry,metabolism Humans Protease Inhibitors/chemistry,metabolism,pharmacology
Chemicals
Protease Inhibitors Epoxide Hydrolases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Morisseau Christophe
Department of Entomology and U.C. Davis Cancer Center, University of California, Davis, California 95616, USA.
Hammock Bruce D
Article Info
Journal
Annual review of pharmacology and toxicology
Abbr.
Annu Rev Pharmacol Toxicol
ISSN
0362-1642
Published
2005-00-00
Pages
311-33
Language
English
Region
United States
NLM ID
7607088
Subset
IM
Grants
NIEHS NIH HHS · P30 ES05707 · United States
NIEHS NIH HHS · P42 ES04699 · United States
NHLBI NIH HHS · R01 HL59699-06A1 · United States
NIEHS NIH HHS · R37 ES02710 · United States
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