Table 11.
Compound | IC50 luciferase refolding (µM) 1 | IC50 MCF7 proliferation (µM) 2 |
---|---|---|
Anthothecol | 12 ± 2 | 0.5 ± 0.06 |
Rottlerin | 63 ± 5 | 7 ± 3 |
Garcinol | 12 ± 5 | 4 ± 0.6 |
Piplartine | 80 ± 7 | 10 ± 3 |
1 Anthothecol, rottlerin, garcinol and piplartine were titrated into wells containing denatured luciferase and reticulocyte lysate. After a two-hour incubation period, assay buffer containing luciferin was added, and relative luminescence was measured. IC50 is the concentration of the compound that inhibited luciferase refolding by 50% compared to the DMSO control; 2 MCF-7 cells were treated in culture with anthothecol, rottlerin, garcinol and piplartine and DMSO as a control. Proliferation was assessed at 48 h using an MTS assay. Proliferation is defined as the colorimetric intensity difference between wells treated with DMSO and wells treated with the compounds.