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Elkaeed, Eslam B.; Taghour, Mohammed S.; Mahdy, Hazem A.; Eldehna, Wagdy M.; El-Deeb, Nehal M.; Kenawy, Ahmed M.; A. Alsfouk, Bshra; Dahab, Mohammed A.; Metwaly, Ahmed M.; Eissa, Ibrahim H.; El-Zahabi, Mohamed A.
Journal of enzyme inhibition and medicinal chemistry, 12/2022, Volume: 37, Issue: 1Journal Article
New quinoline and isatin derivatives having the main characteristics of VEGFR-2 inhibitors was synthesised. The antiproliferative effects of these compounds were estimated against A549, Caco-2, HepG2, and MDA-MB-231. Compounds 13 and 14 showed comparable activities with doxorubicin against the Caco-2 cells. These compounds strongly inhibited VEGFR-2 kinase activity. The cytotoxic activities were evaluated against Vero cells. Compound 7 showed the highest value of safety and selectivity. Cell migration assay displayed the ability of compound 7 to prevent healing and migration abilities in the cancer cells. Furthermore, compound 7 induced apoptosis in Caco-2 through the expressive down-regulation of the apoptotic genes, Bcl2, Bcl-xl, and Survivin, and the upregulation of the TGF gene. Molecular docking against VEGFR-2 emerged the interactions of the synthesised compounds in a similar way to sorafenib. Additionally, seven molecular dynamics simulations studies were applied and confirmed the stability of compound 13 in the active pocket of VEGFR-2 over 100 ns.
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