Design, Synthesis, and Biological Evaluation of New Benzimidazole-1,2,4-Triazole Derivatives as Potential Anticancer Agents

被引:0
作者
Kaya-Sezginer, Ecem [1 ]
Bedir, Beyza Ecem Oz [2 ,3 ]
Terzi, Emine [2 ,3 ]
Sanci, Tuba Ozdemir [3 ,4 ]
Maryam, Zahra [5 ]
Cevik, Ulviye Acar [5 ]
机构
[1] Ankara Univ, Fac Pharm, Dept Biochem, Ankara, Turkiye
[2] Ankara Yildirim Beyazit Univ, Fac Med, Dept Med Biol, Ankara, Turkiye
[3] Ankara Yildirim Beyazit Univ, Yenimahalle Training & Res Hosp, Ankara, Turkiye
[4] Ankara Yildirim Beyazit Univ, Fac Med, Dept Histol & Embryol, Ankara, Turkiye
[5] Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, Eskisehir, Turkiye
关键词
1,2,4-triazole; anticancer activity; apoptosis; benzimidazole; caspase; 3/7; activation; BENZIMIDAZOLE DERIVATIVES; CELL-CYCLE;
D O I
10.1111/cbdd.70033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
New series of benzimidazole-1,2,4-triazole derivatives were designed, synthesized, and characterized using 1H-NMR, 13C-NMR, and HRMS. These compounds were evaluated for anticancer activity toward HTB-9 bladder and HT-29 colorectal cancer cell lines. Compounds 7h and 7 & imath; were found to be the most active against HTB-9 cell line, with IC50 6.27 and 6.44 mu M, respectively, comparable to positive control cisplatin (IC50 = 11.40 mu M). Additionally, in HT-29 cell line, compounds 7a and 7 & imath; exhibited the lowest IC50 values (20.37 and 22.71 mu M, respectively), which was higher than those of cisplatin (19.79 mu M). All active compounds induced apoptosis and caspase 3/7 activity and reduced the migration ability in both cell lines. Particularly, HT-29 cells treated with compound 7 & imath; exerted a higher apoptotic index than cisplatin-treated cells. Furthermore, compounds 7h and 7 & imath; led to G1 cell cycle arrest of HTB-9, and compounds 7a and 7 & imath; against HT-29 induced S and G1 cell cycle arrest, respectively. In conclusion, the antiproliferative effect of active compounds is associated with the induction of apoptosis through caspase 3/7 activation and cell cycle arrest at different phases in HTB-9 and HT-29 cell lines.
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页数:13
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