Skip to main content
. Author manuscript; available in PMC: 2009 Aug 3.
Published in final edited form as: Bioorg Med Chem. 2007 Nov 26;16(4):2114–2130. doi: 10.1016/j.bmc.2007.10.081

Figure 3.

Figure 3

Effect of alkyl chain length and sulfur oxidation state upon inhibitor potency for A) porcine esterase and B) fatty acid amide hydrolase, FAAH. IC50 values were measured following either 5 or 15 min incubation of enzyme and inhibitor. Results are shown as the average ± standard deviation of 3 replicates (error bars are not viewable due to the logarithmic scale, average RSD = 5.4% for esterase and 8% for FAAH). Linear regression values (r2) for the FAAH curves for R = 6, 8, 10 and 12 carbons were: 5 min 0.94, 0.64, 0.46 and 0.41, respectively; 15 min 0.72, 0.45, 0.47 and 0.48, respectively. If an exponential fit was used, the 15 min values were: 0.99, 0.82, 0.69 and 0.62, respectively. The general inhibitor scaffolding is shown in the insert of graph B, with X being thioether, sulfoxide or sulfone as shown in Figure 1. The graph symbols are: Inline graphic Sulfone 5 min, Inline graphic Sulfone 15 min, Inline graphic Sulfoxide 5 min, Inline graphic Sulfoxide 15 min, Inline graphic Thioether 5 min, Inline graphic Thioether 15 min