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- W2979049134 abstract "In this study, new chalcone compounds having the chemical structure of 6-(3-aryl-2-propenoyl)-2(3H)-benzoxazolones (1–8) were synthesised and were characterised by 1H-NMR, 13 C-NMR, and HRMS spectra. Cytotoxic and carbonic anhydrase (CA) inhibitory effects of the compounds were investigated. Cytotoxicity results pointed out that compound 4, 6-[3-(4-trifluoromethylphenyl)-2-propenoyl]-3H-benzoxazol-2-one, showed the highest cytotoxicity (CC50) and potency-selectivity expression (PSE) value, and thus can be considered as a lead compound of this study. According to the CA inhibitory results, IC50 values of the compounds 1–8 towards hCA I were in the range of 29.74–69.57 µM, while they were in the range of 18.14 – 48.46 µM towards hCA II isoenzyme. Ki values of the compounds 1–8 towards hCA I were in the range of 28.37 ± 6.63–70.58 ± 6.67 µM towards hCA I isoenzyme and they were in the range of 10.85 ± 2.14 – 37.96 ± 2.36 µM towards hCA II isoenzyme." @default.
- W2979049134 created "2019-10-10" @default.
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- W2979049134 date "2019-01-01" @default.
- W2979049134 modified "2023-10-18" @default.
- W2979049134 title "Synthesis, cytotoxicities, and carbonic anhydrase inhibition potential of 6-(3-aryl-2-propenoyl)-2(<i>3H</i>)-benzoxazolones" @default.
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- W2979049134 doi "https://doi.org/10.1080/14756366.2019.1670657" @default.
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