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. 2016 Nov 18;21(11):1572. doi: 10.3390/molecules21111572

Table 2.

Structures and cytotoxicity of compounds 13al against HT-29, H-460, A-549, and MDA-MB-231 cells in vitro.

Compd. R1 IC50 (μM) a
HT-29 H-460 A549 MDA-MB-231
13a H 30.52 ± 2.56 28.64 ± 1.08 44.83 ± 2.42 32.16 ± 1.59
13b 2,4-diCH3 45.08 ± 1.37 NA NA NA
13c 2-Cl, 6-CH3 12.95 ± 0.68 24.66 ± 0.80 30.71 ± 1.73 25.42 ± 1.14
13d 2,6-diCH3 18.37 ± 0.45 24.62 ± 2.75 15.94 ± 0.95 28.12 ± 2.44
13e 2,6-diF 35.10 ± 2.81 ND NA 20.94 ± 1.63
13f 3-Cl, 4-F 6.33 ± 0.93 15.28 ± 1.19 10.49 ± 2.26 12.75 ± 2.97
13g 3-Cl 10.07 ± 0.32 5.86 ± 1.34 15.43 ± 1.02 21.95 ± 2.58
13h 3-CF3 ND ND ND ND
13i 4-OCF3 26.58 ± 1.27 23.46 ± 2.29 16.54 ± 0.70 30.65 ± 3.06
13j 4-F 17.95 ± 0.94 32.28 ± 2.87 ND NA
13k 3-F 30.50 ± 3.16 ND NA NA
13l 2-F 24.18 ± 1.35 32.29 ± 2.63 NA 35.56 ± 2.85
Sorafenib 3.27 ± 0.32 2.15 ± 0.43 4.47 ± 0.28 3.81 ± 0.50

a Results are expressed as means ± SD (standard deviation) of three independent experiments. NA: compound showing IC50 value > 50 μM. ND: Not determined.