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. 2013 Dec 11;2013:524701. doi: 10.1155/2013/524701

Table 4.

IC50 (µm) valuesa of the ligands HTSC1–5, palladium(II) complexes [Pd(TSC1–5)2], and cisplatin against the different human tumor cell linesb.

Human tumor cell lines H460 DU145 MCF-7 M14 HT-29 K562
HTSC1 >250 >250 >250 >250 >250 70.86
HTSC2 >250 31.55 38.05 >250 >250 32.89
HTSC3 23.48 26.64 34.00 28.67 25.73 35.05
HTSC4 39.65 26.45 29.94 >250 >250 24.66
HTSC5 24.95 31.60 25.46 27.31 26.72 27.76
[Pd(TSC1)2] 9.40 8.27 6.95 9.87 8.20 9.43
[Pd(TSC2)2] 2.26 2.05 1.61 2.14 1.87 1.95
[Pd(TSC3)2] 0.23 0.01 0.13 0.05 0.05 0.02
[Pd(TSC4)2] 2.05 2.39 2.14 2.27 2.37 1.84
[Pd(TSC5)2] 0.68 0.84 0.78 1.06 1.04 0.65
cisplatin 2.85 6.50 7.20 2.95 7.60 3.20

aIC50 corresponds to the concentration required to inhibit 50% of the cell growth when the cells are exposed to the compounds during 48 h. Each value is the average of two independent experiments.

bLung large cell carcinoma (H460), prostate carcinoma (DU145), breast adenocarcinoma (MCF-7), amelanotic melanoma (M-14), colon adenocarcinoma (HT-29), and chronic myelogenous leukemia (K562).