2,2′-Dihydroxychalcone is a potent apoptosis inducer primarily targeting glutathione S-transferase (GST) with an IC50 of 28.9 μM in human colon cancer cells. This flavonoid has been shown to induce cell cycle arrest and apoptosis specifically in prostate cancer cells, highlighting its potential in cancer therapeutics. Additionally, 2,2′-Dihydroxychalcone exhibits significant anticancer and anti-inflammatory properties, making it a valuable reagent for cancer research and inflammation studies.
2,2′-Dihydroxychalcone is a potent apoptosis inducer primarily targeting glutathione S-transferase (GST) with an IC50 of 28.9 μM in human colon cancer cells. This flavonoid has been shown to induce cell cycle arrest and apoptosis specifically in prostate cancer cells, highlighting its potential in cancer therapeutics. Additionally, 2,2′-Dihydroxychalcone exhibits significant anticancer and anti-inflammatory properties, making it a valuable reagent for cancer research and inflammation studies.
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