| Literature DB >> 21211973 |
Sampath-Kumar Anandan1, Heather Kay Webb, Dawn Chen, Yi-Xin Jim Wang, Basker R Aavula, Sylvaine Cases, Ying Cheng, Zung N Do, Upasana Mehra, Vinh Tran, Jon Vincelette, Joanna Waszczuk, Kathy White, Kenneth R Wong, Le-Ning Zhang, Paul D Jones, Bruce D Hammock, Dinesh V Patel, Randall Whitcomb, D Euan MacIntyre, James Sabry, Richard Gless.
Abstract
1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea 14a (AR9281), a potent and selective soluble epoxide hydrolase inhibitor, was recently tested in a phase 2a clinical setting for its effectiveness in reducing blood pressure and improving insulin resistance in pre-diabetic patients. In a mouse model of diet induced obesity, AR9281 attenuated the enhanced glucose excursion following an intraperitoneal glucose tolerance test. AR9281 also attenuated the increase in blood pressure in angiotensin-II-induced hypertension in rats. These effects were dose-dependent and well correlated with inhibition of the sEH activity in whole blood, consistent with a role of sEH in the observed pharmacology in rodents.Entities:
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Year: 2010 PMID: 21211973 PMCID: PMC3529200 DOI: 10.1016/j.bmcl.2010.12.042
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823