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

被引:0
作者
Leila Emami
Sara Sadeghian
Ayyub Mojaddami
Soghra khabnadideh
Amirhossein Sakhteman
Hossein Sadeghpour
Zeinab Faghih
Masood Fereidoonnezhad
Zahra Rezaei
机构
[1] Shiraz University of Medical Sciences,Pharmaceutical Sciences Research Center, School of Pharmacy
[2] Shiraz University of Medical Sciences,Department of Medicinal Chemistry, School of Pharmacy
[3] Ahvaz Jundishapur University of Medical Sciences,Department of Medicinal Chemistry, School of Pharmacy
[4] Ahvaz Jundishapur University of Medical Sciences,Toxicology Research Center, Medical Basic Sciences Research Institute
来源
BMC Chemistry | / 16卷
关键词
1,2,4-Triazole; Anticancer; MTT assay; Molecular docking; ADME;
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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, 1H-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 μM 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.
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