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. 2019 Jan 17;34(1):465–478. doi: 10.1080/14756366.2018.1555536

Table 2.

Cytotoxicity of the selected compounds against some human cancer cell lines.

graphic file with name IENZ_A_1555536_ILG0002.jpg

Cpd code R R’/Ar MW LogPa Cytotoxicity (IC50,b μM)/Cell linesc
SW620 PC3 NCI-H23
5b -H 2-Cl 340.76 1.52 3.14 ± 0.56 3.99 ± 0.15 4.49 ± 0.24
5l -H 2,4-(OH)2 338.32 0.63 9.43 ± 0.27 16.52 ± 0.24 18.97 ± 3.43
5n -H 2-OH-4-OCH3 352.34 1.19 6.10 ± 0.68 8.46 ± 1.28 9.85 ± 1.28
5t -Cl 4-OCH3 370.79 1.60 2.45 ± 0.03 3.10 ± 0.32 3.34 ± 0.32
5u -CH3 -H 320.35 1.42 3.52 ± 0.03 5.78 ± 0.06 9.77 ± 0.31
5x -CH3 4-OCH3 350.37 1.50 4.99 ± 0.37 4.22 ± 0.63 4.05 ± 0.31
5z -CH3 4-(NCH3)2 363.41 1.60 4.68 ± 0.30 4.60 ± 0.33 3.58 ± 0.11
7b -I -H 473.22 1.21 3.97 ± 0.32 3.25 ± 0.15 2.81 ± 0.17
5-FUd   130.08 −0.81 8.84 ± 1.92 13.61 ± 0.46 13.45 ± 3.92
PAC-1   392.49 3.43 5.82 ± 0.20 4.16 ± 0.52 5.32 ± 0.21

aCalculated by EPI 320 software; bThe concentration (µM) of compounds that produces a 50% reduction in enzyme activity or cell growth, the numbers represent the averaged results from triplicate experiments with deviation of less than 10%.; cCell lines: SW620, colon cancer; PC3, prostate cancer; NCI-H23, lung cancer; d5-FU: 5-Fluorouracil, a positive control.