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• W3109057752 endingPage "104511" @default.
• W3109057752 startingPage "104511" @default.
• W3109057752 abstract "• Novel quinoline analogues bearing thiazolidinones were designed and synthesized. • 15i possessing potent inhibitory activity against multi-kinases was identified. • Antitumor activity on HT-29 of 15i was 14.5-fold more potent than that of Regorafenib. • The toxicity to FHC cells of 15i was much lower than that of Regorafenib. In this study, a novel series of 4,6,7-trisubstituted quinoline analogues bearing thiazolidinones were designed and synthesized based on our previous study. Among them, the most potent compound 15i , 4-((4-(4-(3-(2-(2,6-difluorophenyl)-4-oxothiazolidin-3-yl)ureido)-2-fluorophenoxy)-6-methoxyquinolin-7-yl)oxy)- N,N -diethylpiperidine-1-carboxamide was identified as a multi-kinase inhibitor. The results of MTT assay revealed in vitro antitumor activities against HT-29 cells of compound 15i with an IC 50 value of 0.19 μM which was 14.5-fold more potent than that of Regorafenib. In the cellular context, significant antiproliferation, cytotoxicity and induction of apoptosis on HT-29 cells in a dose- and time-dependent manner were confirmed by IncuCyte live-cell imaging assays. Moreover, compound 15i strongly induced apoptosis by arresting cell cycle into the G2/M phase. No antiproliferation and cytotoxicity against human normal colorectal mucosa epithelial cell FHC was observed at 10.0 μg/mL or lower concentrations which indicated that the toxicity to normal cells of compound 15i was much lower than that of Regorafenib. Based on the above findings, further structural modification will be conducted for the development of more potent kinase inhibitors as anticancer agents." @default.
• W3109057752 created "2020-12-07" @default.
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• W3109057752 date "2021-01-01" @default.
• W3109057752 modified "2023-10-17" @default.
• W3109057752 title "Discovery of 4-((4-(4-(3-(2-(2,6-difluorophenyl)-4-oxothiazolidin-3-yl)ureido)-2-fluorophenoxy)-6-methoxyquinolin-7-yl)oxy)-N,N-diethylpiperidine-1-carboxamide as kinase inhibitor for the treatment of colorectal cancer" @default.
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• W3109057752 doi "https://doi.org/10.1016/j.bioorg.2020.104511" @default.
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