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