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. Author manuscript; available in PMC: 2013 Sep 15.
Published in final edited form as: Bioorg Med Chem Lett. 2012 Aug 2;22(18):5889–5892. doi: 10.1016/j.bmcl.2012.07.074

Table 2.

Inhibition of human sEH of 3-(3-adamantan-1-yl-ureido)-cyclohexylcarboxylic acid derivatives.

Compound Structure Human sEH IC50 (nM)a
10 graphic file with name nihms-398848-t0008.jpg 1160
11 graphic file with name nihms-398848-t0009.jpg 2
12 graphic file with name nihms-398848-t0010.jpg 3
13 graphic file with name nihms-398848-t0011.jpg 9
a

Human sEH (0.96 nM) was incubated with inhibitors for 5 min in 25 mM Bis-Tris/HCl buffer (200 μL; pH 7.0) at 30°C before fluorescent substrate introduction ([S] = 5 μM). Results are averages of three separate measurements. The fluorescent assay as performed here has a standard error between 10 and 20%, suggesting that differences of 2-fold or greater are significant.