Structure−Activity Relationships of Cycloalkylamide Derivatives as Inhibitors of the Soluble Epoxide Hydrolase-Reference-Cited by-同舟云学术

Structure−Activity Relationships of Cycloalkylamide Derivatives as Inhibitors of the Soluble Epoxide Hydrolase

Published:2011-02-21 Issue:6 Volume:54 Page:1752-1761
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Kim In-Hae¹,Park Yong-Kyu²,Hammock Bruce D.³,Nishi Kosuke⁴

Affiliation:

1. Industry and Academic Cooperation Laboratory for Drug Development, Mokpo National University, Muan, Jeonnam 534-729, Republic of Korea

2. Department of Medicinal Chemistry, Hyundai Pharma, Suwon, Gyeonggi 443-270, Republic of Korea

3. Department of Entomology and University of California Davis Cancer Center, University of California, One Shields Avenue, Davis, California 95616, United States

4. Department of Applied Bioscience, Faculty of Agriculture, Ehime University, 3-5-7 Tarumi, Matsuyama, Ehime 790-8566, Japan

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm101431v

Reference33 articles.

1. Cytochrome P450 and arachidonic acid bioactivation: molecular and functional properties of the arachidonate monooxygenase

2. Soluble Epoxide Hydrolase Regulates Hydrolysis of Vasoactive Epoxyeicosatrienoic Acids

3. Soluble Epoxide Hydrolase Inhibition Lowers Arterial Blood Pressure in Angiotensin II Hypertension

4. Soluble Epoxide Hydrolase Is a Main Effector of Angiotensin II–Induced Hypertension

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