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. 2014 Sep 26;19(10):15361–15373. doi: 10.3390/molecules191015361

Table 2.

In vitro growth inhibition of selected tumor cell lines by some benzimidazole-4,7-diones.

Compounds IC50 [μM] Differential Cytotoxicity O/H
Normoxia (O) Hypoxia (H)
1a A549 30.2 ± 1.2 36.1 ± 1.2 0.83
WM 115 26.4 ± 1.6 32.5 ± 1.2 0.81
1b A549 100.0 ± 1.8 47.4 ± 1.1 2.13
WM 115 101.0 ± 1.2 45.8 ± 1.8 2.20
1c A549 80.9 ± 1.9 51.2 ± 1.5 1.58
WM 115 77.9 ± 1.3 48.5 ± 1.3 1.60
1d A549 479.5 ± 3.6 232.4 ± 1.4 2.06
WM 115 399.5 ± 2.2 229.2 ± 0.4 1.74
2a A549 115.7 ± 1.9 35.0 ± 1.6 3.28
WM 115 105.0 ± 0.7 33.0 ± 1.9 3.18
2b A549 500.6 ± 1.2 116.0 ± 0.8 4.31
WM 115 490.6 ± 1.9 115.0 ± 1.2 4.26
2c A549 79.5 ± 1.9 44.0 ± 2.5 1.80
WM 115 65.5 ± 1.3 40.0 ± 2.0 1.63
2d A549 252 ± 2.5 96.8 ± 1.9 2.59
WM 115 189 ± 1.5 95.2 ± 2.1 1.98
T A549 166.2 ± 1.6 36.0 ± 1.2 4.61
WM 115 156.2 ± 1.6 34.0 ± 1.2 4.59

WST-1 assay was used to determine the inhibition of the cell growth. After a 48 h incubation with the tested compounds. IC50 values (concentration of the tested compounds causing. 50% inhibition of the cell growth compared to control cells) were calculated and expressed as the mean ± SD, n = 3.