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新型1,2,4-三唑衍生物作为有前景的抗癌药物的设计、合成与评价

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

作者信息

Emami Leila, Sadeghian Sara, Mojaddami Ayyub, Khabnadideh Soghra, Sakhteman Amirhossein, Sadeghpour Hossein, Faghih Zeinab, Fereidoonnezhad Masood, Rezaei Zahra

机构信息

Pharmaceutical Sciences Research Center, School of Pharmacy, Shiraz University of Medical Sciences, P.O. Box: 71345-1798, Shiraz, Iran.

Department of Medicinal Chemistry, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

BMC Chem. 2022 Nov 12;16(1):91. doi: 10.1186/s13065-022-00887-x.

Abstract

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-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.

摘要

在此,我们报道了19种新型1,2,4-三唑衍生物的合成,包括1,3-二苯基-2-(1H-1,2,4-三唑-1-基)丙-1-酮(7a - e)、1-(1,3-二苯基丙-2-基)-1H-1,2,4-三唑(8a - c)和1,4-二苯基-2-(1H-1,2,4-三唑-1-基)丁烷-1,4-二酮(10a - k)。这些衍生物的结构通过红外光谱、氢核磁共振、质谱和元素分析等光谱技术得到证实。使用MTT法评估了合成化合物对三种人类癌细胞系(包括MCF-7、Hela和A549)的细胞毒性活性。化合物7d、7e、10a和10d对Hela细胞系表现出有前景的细胞毒性活性,其活性低于12μM。还以MRC-5作为正常细胞系评估了这些化合物的安全性,结果表明大多数合成化合物对正常细胞系和细胞毒性癌细胞系具有适当的选择性。最后,还进行了分子对接研究,以了解这些衍生物在作为可能靶点的芳香化酶结合口袋中的作用机制和结合模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1e/9652805/7e7667b276d9/13065_2022_887_Fig1_HTML.jpg

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