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ID: ALA1137287

Journal: Bioorg Med Chem Lett

Title: Peptidyl-urea based inhibitors of soluble epoxide hydrolases.

Authors: Morisseau C, Newman JW, Tsai HJ, Baecker PA, Hammock BD.

Abstract: We prepared a series of amino acid derived cyclohexyl and adamantyl ureas and tested them as inhibitors of the human soluble epoxide hydrolase, and obtained very potent compounds (K(I)=15nM) that are >10-fold more soluble than previously described sEH inhibitors. While our lead compound 2 showed low apparent bioavailability in dogs and rats, this series of compounds revealed that sEH inhibitor structures could accept large groups that could lead to better orally available drugs.

CiteXplore: 16908134

DOI: 10.1016/j.bmcl.2006.07.073