Cells were plated at a density of 5000 cells in triplicates in a 96-well plate. On the next day, treatment of the cells was performed with the indicated compound/s at the specified concentrations in 100 μL media as a final volume. Cell viability was considered after 72 h using MTT solution (Promega, Madison, WI, USA) [28 (link)]. The reagent (20 μLs) was added to each well followed by incubation of the plate for 3 h and fluorescence was subsequently measured (570 nm) using a plate reader, then IC50 values were assessed using the GraphPad prism 7 [29 (link),30 (link)].
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