Inhibitory properties of human DNA topoisomerase IIα for the tested piperidinecarboxamides, Methotrexate and Combretastatin.
Entry | Compound | IC50 (μM ± SD)a |
---|---|---|
1 | 27 | 33.64 ± 1.30 |
2 | 29 | 28.97 ± 1.39 |
3 | 30 | 41.79 ± 2.42 |
4 | 34 | 30.69 ± 1.32 |
5 | 35 | 26.39 ± 1.61 |
6 | 36 | 23.04 ± 1.37 |
7 | 37 | 27.23 ± 1.72 |
8 | 38 | 35.01 ± 2.08 |
9 | 39 | 41.30 ± 1.60 |
10 | 40 | 40.35 ± 1.56 |
11 | 41 | 50.17 ± 1.94 |
12 | 42 | 31.49 ± 1.22 |
13 | 43 | 28.30 ± 1.09 |
14 | 44 | 46.18 ± 1.79 |
15 | 45 | 39.31 ± 1.52 |
16 | 46 | 56.23 ± 2.18 |
17 | 47 | 33.01 ± 1.28 |
18 | Methotrexate (Met) | 23.25 ± 1.31 |
19 | Combretastatin A-4 (CA-4) | 22.02 ± 0.85 |
IC50 is the concentration producing 50% inhibition of the tested enzyme, SD is the standard division.