Design, synthesis and evaluation of novel 1,2,4-triazole derivatives as promising anticancer agents

被引:17
作者
Emami, Leila [1 ]
Sadeghian, Sara [2 ]
Mojaddami, Ayyub [3 ,4 ]
Khabnadideh, Soghra [1 ,2 ]
Sakhteman, Amirhossein [2 ]
Sadeghpour, Hossein [2 ]
Faghih, Zeinab [1 ]
Fereidoonnezhad, Masood [3 ]
Rezaei, Zahra [1 ,2 ]
机构
[1] Shiraz Univ Med Sci, Pharmaceut Sci Res Ctr, Sch Pharm, POB 71345-1798, Shiraz, Iran
[2] Shiraz Univ Med Sci, Sch Pharm, Dept Med Chem, Shiraz, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Sch Pharm, Dept Med Chem, Ahvaz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Toxicol Res Ctr, Med Basic Sci Res Inst, Ahvaz, Iran
关键词
1; 2; 4-Triazole; Anticancer; MTT assay; Molecular docking; ADME; BIOLOGICAL EVALUATION; MOLECULAR DOCKING; TRIAZOLE DERIVATIVES; AROMATASE INHIBITORS; 1,2,3-TRIAZOLES; COMPLEXES;
D O I
10.1186/s13065-022-00887-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we reported the synthesis of nineteen novel 1,2,4-triazole derivatives including 1,3-diphenyl-2-(1H-1,2,4-triazol-1-yl) propan-1-ones (7a-e), 1-(1,3-diphenylpropan-2-yl)-1H-1,2,4-triazole (8a-c) and 1,4-diphenyl-2-(1H-1,2,4-triazol-1-yl) butane-1,4-diones (10a-k). The structures of these derivatives were confirmed by spectroscopic techniques like IR, H-1-NMR, Mass spectroscopy and Elemental analysis. The cytotoxic activities of the synthesized compounds were evaluated against three human cancer cell lines including MCF-7, Hela and A549 using MTT assay. Compounds 7d, 7e, 10a and 10d showed a promising cytotoxic activity lower than 12 mu M against Hela cell line. The safety of these compounds was also, evaluated on MRC-5 as a normal cell line and relieved that most of the synthesized compounds have proper selectivity against normal and cytotoxic cancerous cell lines. Finally, molecular docking studies were also, done to understand the mechanism and binding modes of these derivatives in the binding pocket of aromatase enzyme as a possible target.
引用
收藏
页数:18
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