Cells were seeded in 96-well plate (1 × 104 cells/well). Cells were treated with different concentrations of compounds or DMSO as a control for 24 h. Caspase 3/7 activity was assessed by the Caspase-Glo 3/7 Assay kit (Promega), following the manufacturer's protocol. Bioluminescence imaging was measured using the IVIS imager. Caspase activity was normalized to cell numbers and compared to those of the DMSO treatment control in each cell line. Data is reported as mean RLU + SEM (n = 3).

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