Aziridine-Functionalized 1,3,5-Triazine Derivatives as Promising Anticancer Agents: Synthesis, DFT Study, DNA Binding Investigations and In Vitro Cytotoxic Activity

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC
Aleksandra V. Protas, Olga V. Mikolaichuk, Еlena А. Popova, Kirill V. Timoshchuk, Ilya V. Kornyakov, Dmitrii N. Maistrenko, Oleg E. Molchanov, Vladimir V. Sharoyko, Konstantin N. Semenov
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引用次数: 0

Abstract

Herein, we report a synthesis and characterization of aziridine-functionalized 1,3,5-triazine derivatives. Electronic structure and the most preferable geometry of substances were calculated by DFT method. DNA binding investigations were conducted as part of the biomedicinal research as well as the cytotoxic activity of these compounds was evaluated using in vitro assays toward Huh-7 and A549 cancer cell lines and HEK-293 normal cell line. The results demonstrate that some of the synthesized compounds exhibit potent cytotoxic activity ([5-[[4,6-bis(aziridin-1-yl)-1,3,5-triazin-2-yl]amino]-2,2-dimethyl-1,3-dioxan-5-yl]methanol (1) and 4,6-di(aziridine-1-yl)-N-(2,2,5-trimethyl-1,3-dioxane-5-yl)-1,3,5-triazine-2-amine (9)), making them potential candidates for further development as anticancer agents.

氮丙啶官能化 1,3,5-三嗪衍生物作为有前途的抗癌剂:合成、DFT 研究、DNA 结合研究和体外细胞毒性活性
在此,我们报告了氮丙啶功能化 1,3,5 三嗪衍生物的合成和表征。通过 DFT 方法计算了这些物质的电子结构和最理想的几何形状。作为生物医学研究的一部分,我们对这些化合物进行了 DNA 结合研究,并通过体外实验评估了它们对 Huh-7 和 A549 癌细胞系以及 HEK-293 正常细胞系的细胞毒性活性。结果表明,合成的一些化合物具有很强的细胞毒性([5-[[4,6-双(氮丙啶-1-基)-1,3,5-三嗪-2-基]氨基]-2,2-二甲基-1、3-二恶烷-5-基]甲醇 (1) 和 4,6-二(氮丙啶-1-基)-N-(2,2,5-三甲基-1,3-二恶烷-5-基)-1,3,5-三嗪-2-胺 (9)),使它们成为进一步开发抗癌剂的潜在候选物质。
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来源期刊
Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
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