20 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
24035338	82	Discovery of 2,8-diazaspiro[4.5]decane-based trisubstituted urea derivatives as highly potent soluble epoxide hydrolase inhibitors and orally active drug candidates for treating hypertension.	Toray Industries
21354674	14	The many faces of the adamantyl group in drug design.	University of Sydney
19645482	245	Discovery of a highly potent, selective, and bioavailable soluble epoxide hydrolase inhibitor with excellent ex vivo target engagement.	Merck Research Laboratories
17616115	61	Orally bioavailable potent soluble epoxide hydrolase inhibitors.	University of California Davis
21211973	35	1-(1-acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia.	Ar£Te Therapeutics
20812725	103	1-Aryl-3-(1-acylpiperidin-4-yl)urea inhibitors of human and murine soluble epoxide hydrolase: structure-activity relationships, pharmacokinetics, and reduction of inflammatory pain.	Department of Entomology and University of California Davis Cancer Center
17046265	66	Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase.	Department of Entomology and University of California Davis Cancer Center
16908134	98	Peptidyl-urea based inhibitors of soluble epoxide hydrolases.	University of California
15887969	64	Optimization of amide-based inhibitors of soluble epoxide hydrolase with improved water solubility.	Department of Entomology and University of California Davis Cancer Center
15056008	72	Design, synthesis, and biological activity of 1,3-disubstituted ureas as potent inhibitors of the soluble epoxide hydrolase of increased water solubility.	University of California Davis
12620084	17	QSAR and classification of murine and human soluble epoxide hydrolase inhibition by urea-like compounds.	The Pennsylvania State University
31436984	54	Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase Domain.	Goethe-University Frankfurt
31488357	19	Exploring the size of the lipophilic unit of the soluble epoxide hydrolase inhibitors.	Universitat De Barcelona
8423594	39	Development of selective tight-binding inhibitors of leukotriene A4 hydrolase.	Scripps Research Institute
29366648	98	Identification and optimization of soluble epoxide hydrolase inhibitors with dual potency towards fatty acid amide hydrolase.	University of California Davis
29803731	68	Adamantyl thioureas as soluble epoxide hydrolase inhibitors.	University of California Davis