Table 2. IC 50 values for the inhibitory effects of the test drugs (compounds and reference inhibitors) on the enzymatic activity of human MAO-B (rational assays selected by our modeling), human MAO-A (control assays not selected by the modeling) and human COX-1 (control assays not selected by the modeling).
DRUG | IC50 hMAO-B (μM) | IC50 hMAO-A (μM) | IC50 hCOX-1 (μM) |
---|---|---|---|
Piperlongumine | 65.07 ± 2.99 | ** | ** |
Frentizole | ** | ** | ** |
Ethoxzolamide | 24.57 ± 1.09 | ** | ** |
Selegiline (Reference inhibitor) | 0.019 ± 0.001 | ||
Iproniazide (Reference inhibitor) | 7.54 ± 0.36 | 6.56 ± 0.76 | |
Moclobemide (Reference inhibitor) | 0.36 ± 0.02 | ||
FR122047 (Reference inhibitor) | 0.094 ± 0.006 |
Each IC50 value is the mean ± S.E.M. from three experiments (n = 3). ** Inactive at 100 μM (highest concentration tested).