Table 2. Antiproliferative Activities of 3a–ja.
GI50 (μM) |
||||
---|---|---|---|---|
compd | A549 | MCF-7 | MDA-MB-231 | MDA-MB-468 |
3a | 0.29 ± 0.01 | 0.14 ± 0.03 | 0.37 ± 0.13 | 0.22 ± 0.07 |
3b | 0.95 ± 0.77 | 1.72 | 1.00 ± 0.58 | 1.62 ± 0.48 |
3c | 2.44 ± 0.40 | 2.30 ± 0.67 | 4.61 ± 2.20 | 1.82 ± 0.20 |
3d | 2.32 ± 0.35 | 2.66 ± 1.30 | 5.82 ± 4.61 | 2.32 ± 0.39 |
3e | >100 | >100 | >100 | 13.74 ± 3.98 |
3f | 0.26 ± 0.06 | 1.65 ± 0.44 | 0.26 ± 0.04 | 0.20 ± 0.02 |
3g | 39.15 ± 32.09 | 28.99 ± 10.27 | 82.67 ± 24.52 | 10.19 ± 1.47 |
3h | 1.16 ± 0.05 | 0.81 ± 0.78 | 1.21 ± 0.15 | 0.25 ± 0.01 |
3i | 0.47 ± 0.06 | 0.31 ± 0.10 | 0.073 ± 0.04 | 0.046 ± 0.04 |
3j | 2.17 ± 0.11 | 1.89 ± 0.60 | 2.71 ± 0.32 | 1.85 ± 0.23 |
GI50 is the concentration required to inhibit the cancer cell growth by 50% as evaluated by the MTT assay. The compounds were incubated with cells for 72 h. The GI50 was presented as mean ± SD of at least two independent experiments in duplicates or >100 in the cases where GI50 was not reached at the highest tested concentration (100 μM). When SD was not presented, only one experiment was performed in duplicate.