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. 2009 Oct 19;14(10):4166–4179. doi: 10.3390/molecules14104166

Table 1.

The substituents of target compounds and their antiproliferative effects in K562 cells.

Compound R GI50 (μM) in K562a
12a H 2.01 ± 0.10
12b 2-F 0.67 ± 0.07
12c 2-Cl 0.10 ± 0.01
12d 2-Br 0.07 ± 0.01
12e 2-NO2 0.26 ± 0.02
12f 2-OCH3 0.83 ± 0.05
12g 2-OCH2CH3 1.55 ± 0.21
12h 4-F 1.83 ± 0.09
12i 4-Cl 1.26 ± 0.04
12j 4-Br 0.55 ± 0.05
12k 4-NO2 0.39 ± 0.04
12l 4-CH3 0.51 ± 0.02
12m 4-OCH3 1.05 ± 0.06
12n 4-OCH2Ph > 5
12o 2,3-di-OCH3 0.14 ± 0.01
12p 2,4-di-OCH3 1.26 ± 0.05
12q 2,3,4-tri-OCH3 0.78 ± 0.06
12r 3,4-di-OCH3 0.99 ± 0.17
12s 3-OCH3,4-OCH2CH3 > 5
12t 3-OCH2CH3,4-OCH3 0.48 ± 0.04
12u 3-OCH3,4-OCH2Ph > 5
12v 3-OCH2Ph,4-OCH3 > 5
12w 3,4(-OCH2O-) 0.57 ± 0.02
15 3.51 ± 0.33
STI-571 0.23 ± 0.01

a GI50 is the concentration that inhibits 50% of cell growth. Cells were seeded at 4.0 × 104 cells/mL and incubated with various concentrations of tested compounds for 72 h. The data shown are the mean ± SE of three independent experiments.