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• W2949936212 abstract "A series of chalcone and flavonol derivatives were synthesized in good yield by an eco-friendly approach. A pharmacological evaluation was performed with the human colorectal carcinoma cell line HCT116 and revealed that the anticancer activity of flavonols was higher when compared with that of the respective chalcone precursors. The antiproliferative activity of halogenated derivatives increases as the substituent in the 3- or 4-positon of the B-ring goes from F to Cl and to Br. In addition, halogens in position 3 enhance anticancer activity in chalcones whereas for flavonol derivatives the best performance was registered for the 4-substituted derivatives. Flow cytometry analysis showed that compounds 3p and 4o induced cell cycle arrest and apoptosis as demonstrated by increased S, G2/M and sub-G1 phases. These data were corroborated by western blot and fluorescence microscopy analysis. In summary, halogenated chalcones and flavonols were successfully prepared and presented high anticancer activity as shown by their cell growth and cell cycle inhibitory potential against HCT116 cells, superior to that of quercetin, used as a positive control." @default.
• W2949936212 created "2019-06-27" @default.
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• W2949936212 date "2013-07-01" @default.
• W2949936212 modified "2023-09-25" @default.
• W2949936212 title "Superior anticancer activity of halogenated chalcones and flavonols over the natural flavonol quercetin" @default.
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• W2949936212 doi "https://doi.org/10.1016/j.ejmech.2013.04.064" @default.
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