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. Author manuscript; available in PMC: 2017 Jun 19.
Published in final edited form as: Bioorg Med Chem Lett. 2016 Apr 6;26(11):2691–2694. doi: 10.1016/j.bmcl.2016.04.006

Table 2.

In vitro cytotoxicity of compounds 3ap

Compound IC50a (μM)
HeLa MDA-MB-231 MiaPaca-2 MCF-7 MCF-10
3a 18.64 IAb IA IA IA
3b 28.31 IA 26.12 32.81 IA
3c 27.19 IA 28.47 32.81 IA
3d 29.00 IA IA IA IA
3e 29.00 IA IA IA IA
3f 28.01 IA 27.08 IA IA
3g 24.12 26.90 26.29 32.81 IA
3h 28.65 29.16 27.32 IA IA
3i 25.15 26.50 26.33 32.13 IA
3j 32.87 28.00 23.19 28.48 IA
3k 27.20 IA IA 31.49 IA
3l 25.79 31.21 26.38 32.19 IA
3m 27.36 28.54 27.44 32.29 IA
3n 25.60 30.71 27.10 31.10 IA
3o 29.12 IA 27.55 31.73 IA
3p IA IA IA IA IA
Shikonin 6.42 3.94 0.04 5.49 4.56
a

IC50 values were calculated from three independent experiments.

b

IA = inactivity. Inactivity is defined as having greater than 50% cell at the highest concentration (33.3 μM).