Synthesis, Antitumor Activity, and Docking Study of 1,3-Disubstituted Imidazolium Derivatives
- 作者: Fan Q.1, Zhong Q.1, Yan H.1
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隶属关系:
- College of Life Science and Bioengineering
- 期: 卷 87, 编号 12 (2017)
- 页面: 3023-3028
- 栏目: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/221838
- DOI: https://doi.org/10.1134/S1070363217120489
- ID: 221838
如何引用文章
详细
A series of 1,3-disubstituted imidazolium salts were synthesized through a convenient synthetic approach based on the reaction of 1,4-diazabuta-1,3-dienes with HClO4. Their antitumor activity was evaluated in vitro against a number of human cancer cells. 1,3-Bis[(3,5-bis(trifluoromethyl)phenyl]imidazolium perchlorate turned out to be the most active against A549 and MCF-7 cancer cell lines with IC50 values of 5.24 and 4.21 μM, respectively. The results of structure–activity relationship study indicated that substituents on the imidazole derivatives play an important role in their cytotoxic activities. Finally, molecular docking of some tested compounds was carried out in order to investigate their binding pattern with the CDK2.
作者简介
Q. Fan
College of Life Science and Bioengineering
Email: hongyan@bjut.edu.cn
中国, Beijing, 100124
Q. Zhong
College of Life Science and Bioengineering
Email: hongyan@bjut.edu.cn
中国, Beijing, 100124
H. Yan
College of Life Science and Bioengineering
编辑信件的主要联系方式.
Email: hongyan@bjut.edu.cn
中国, Beijing, 100124