Novel coumarin-6-sulfonamides as apoptotic anti-proliferative agents: synthesis,in vitro biological evaluation,and QSAR studies |
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Authors: | Ahmed Sabt Omaima M. Abdelhafez Radwan S. El-Haggar Hassan M. F. Madkour Ezz El-Din A. M. El-Khrisy |
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Affiliation: | 1. Chemistry of Natural Compounds Department, National Research Centre, Dokki, Egypt;2. Pharmaceutical Chemistry Department, Faculty of Pharmacy, Helwan University, Cairo, Egypt;3. Chemistry Department, Faculty of Science, Ain-shams University, Cairo, Egypt |
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Abstract: | Herein, we report the synthesis of different novel sets of coumarin-6-sulfonamide derivatives bearing different functionalities (4a, b, 8a–d, 11a–d, 13a, b, and 15a–c), and in vitro evaluation of their growth inhibitory activity towards the proliferation of three cancer cell lines; HepG2 (hepatocellular carcinoma), MCF-7 (breast cancer), and Caco-2 (colon cancer). HepG2 cells were the most sensitive cells to the influence of the target coumarins. Compounds 13a and 15a emerged as the most active members against HepG2 cells (IC50?=?3.48?±?0.28 and 5.03?±?0.39?µM, respectively). Compounds 13a and 15a were able to induce apoptosis in HepG2 cells, as assured by the upregulation of the Bax and downregulation of the Bcl-2, besides boosting caspase-3 levels. Besides, compound 13a induced a significant increase in the percentage of cells at Pre-G1 by 6.4-folds, with concurrent significant arrest in the G2-M phase by 5.4-folds compared to control. Also, 13a displayed significant increase in the percentage of annexin V-FITC positive apoptotic cells from 1.75–13.76%. Moreover, QSAR models were established to explore the structural requirements controlling the anti-proliferative activities. |
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Keywords: | Anticancer Apoptosis Coumarin-6-sulfonamides 2D-QSAR Synthesis |
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