Synthesis, structural characterization and anticancer activity of 3(3,5-dinitrobenzoyl)-1H-imidazolidine-2-thione

被引:0
作者
Genc, Murat [1 ]
Keskin, Ozlem [1 ]
Kumbicak, Zubeyde [2 ]
Vatan, Ozgur [3 ]
Huriyet, Huzeyfe [3 ]
Cavas, Tolga [3 ]
机构
[1] Adiyaman Univ, Fac Arts & Sci, Dept Chem, TR-02040 Adiyaman, Turkey
[2] Nevsehir Haci Bektas Veli Univ, Fac Arts & Sci, Dept Mol Biol & Genet, TR-50300 Nevsehir, Turkey
[3] Uludag Univ, Fac Arts & Sci, Dept Biol, TR-16059 Bursa, Turkey
来源
INDIAN JOURNAL OF CHEMISTRY | 2022年 / 61卷 / 02期
关键词
Imidazole; BRCA2; AutodockVina; cytotoxicity; anticancer; MCF-7; ANALOGS SYNTHESIS; BRCA2; DOCKING; INTERACTS; BINDING;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The present study describes the synthesis, characterization and in vitro anticancer potential evaluation of a novel 3-(3,5-dinitrobenzoyl)-1H-imidazolidine-2-thione compound. In the first step, structure analysis of the compound has been elucidated by NMR and FT-IR techniques. Theoretical NMR, FT-IR spectra, HOMO and LUMO orbital energies and MEP analyses have been used to determine the activity of the molecule by Gaussian 09 package program using DFT techniques. Furthermore, docking calculations have been performed for the BRCA2 (PDB Code: 3EU7) active side to foresee the possible mechanism of action of the synthesized compound. In the second step of the study, the synthesized compound has been screened for its potential in vitro anticancer activity against MCF-7 human breast cancer cell line using the cell proliferation (XTT), apoptosis, cell cycle arrest and intracellular ROS production assays. The results of XTT test revealed significant dereases in MCF-7 cell viability with the 24h IC50 value of 7.57 mu M. It has been also observed that treatment with the IC50 concentration of the compound can significantly induce apoptosis, intracellular ROS production and G2/M phase arrest in MCF-7 cells.
引用
收藏
页码:201 / 209
页数:9
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