Ontology highlight
ABSTRACT:
SUBMITTER: Hwang SH
PROVIDER: S-EPMC2596069 | biostudies-literature | 2007 Aug
REPOSITORIES: biostudies-literature
Journal of medicinal chemistry 20070706 16
A series of N,N'-disubstituted ureas having a conformationally restricted cis- or trans-1,4-cyclohexane alpha to the urea were prepared and tested as soluble epoxide hydrolase (sEH) inhibitors. This series of compounds showed low nanomolar to picomolar activities against recombinant human sEH. Both isomers showed similar potencies, but the trans isomers were more metabolically stable in human hepatic microsomes. Furthermore, these new potent inhibitors show a greater metabolic stability in vivo ...[more]