Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1369875 | Bioorganic & Medicinal Chemistry Letters | 2016 | 5 Pages |
Abstract
A series of novel fluoro-substituted chalcone derivatives have been synthesized. All synthesized compounds were characterized by 1H nuclear magnetic resonance (NMR), 13C NMR, and elemental analysis. Their anti-proliferative activities were evaluated against five cancer cells lines, namely, A549, A498, HeLa, A375, and HepG2 using the MTT method. Most of the compounds showed moderate to high activity with IC50 values in the range of 0.029–0.729 μM. Of all the synthesized compounds, 10 and 19 exhibited the most potent anti-proliferative activities against cancer cells, and 10 was identified as the most promising compound.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Serdar Burmaoglu, Oztekin Algul, Derya Aktas Anıl, Arzu Gobek, Gulay Gulbol Duran, Ronak Haj Ersan, Nizami Duran,