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. 2021 May 12;60(11):7974–7990. doi: 10.1021/acs.inorgchem.1c00507

Table 5. Half-Maximum Inhibitory Concentrationsa (IC50, μM) of Compounds 1I2Me and 2I2 and their Chlorido Counterparts, Respectively [RuCl26-methyl benzoate)(dimethyl(1-pyrenyl)phosphane)] (1Cl2Me) and [RuCl26-p-cymene)(dimethyl(1-pyrenyl)phosphane)] (2Cl2),35 for A549 (Lung Adenocarcinoma), SW620 (Colorectal Adenocarcinoma) and MCF7 (Breast Carcinoma) Human Cells, after Incubation for 24 h.

compound A549 SW620 MCF7
1I2Me 2.6 ± 0.4 9 ± 2 6 ± 1
1Cl2Meb 5.0 ± 0.6 1.9 ± 0.1 5.1 ± 1.6
2I2Me 6.3 ± 0.4 16 ± 4 17 ± 6
2Cl2Meb 17.2 ± 0.5 6.5 ± 0.8 9.7 ± 0.1
a

The results are expressed as mean values ± SD out of three independent experiments.

b

Compounds described in ref (35).