As one of the most lethal malignancies, lung cancer is considered to account for approximately one-fifth of all malignant tumours-related deaths worldwide. This study reports the synthesis and in vitro biological assessment of two sets of 3-methylbenzofurans (4a-d, 6a-c, 8a-c and 11) and 3-(morpholinomethyl)benzofurans (15a-c, 16a-b, 17a-b and 18) as potential anticancer agents towards non-small cell lung carcinoma A549 and NCI-H23 cell lines, with VEGFR-2 inhibitory activity. The target benzofuran-based derivatives efficiently inhibited the growth of both A549 and NCI-H23 cell lines with IC(50) spanning in ranges 1.48-47.02 and 0.49-68.9âµM, respectively. The three most active benzofurans (4b, 15a and 16a) were further investigated for their effects on the cell cycle progression and apoptosis in A549 (for 4b) and NCI-H23 (for 15a and 16a) cell lines. Furthermore, benzofurans 4b, 15a and 16a displayed good VEGFR-2 inhibitory activity with IC(50) equal 77.97, 132.5 and 45.4ânM, respectively.
Development of 3-methyl/3-(morpholinomethyl)benzofuran derivatives as novel antitumor agents towards non-small cell lung cancer cells.
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作者:Al-Sanea Mohammad M, Al-Ansary Ghada H, Elsayed Zainab M, Maklad Raed M, Elkaeed Eslam B, Abdelgawad Mohamed A, Bukhari Syed Nasir Abbas, Abdel-Aziz Marwa M, Suliman Howayda, Eldehna Wagdy M
| 期刊: | Journal of Enzyme Inhibition and Medicinal Chemistry | 影响因子: | 5.400 |
| 时间: | 2021 | 起止号: | 2021 Dec;36(1):987-999 |
| doi: | 10.1080/14756366.2021.1915302 | ||
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