Biological evaluation of 4-aryl-1,4-dihydropyridines as VEGFR-2 kinase inhibitors
- 作者: Sun W.1, Ma Z.1, Yan H.1
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隶属关系:
- College of Life Science and Bioengineering
- 期: 卷 86, 编号 12 (2016)
- 页面: 2891-2899
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/217319
- DOI: https://doi.org/10.1134/S1070363216120574
- ID: 217319
如何引用文章
详细
Vascular endothelial growth factor-2 receptor (VEGFR-2) kinase is a promising target for the development of novel anticancer drugs. Molecular docking modeling was performed on a series of 4-aryl-1,4-dihydropyridines derivatives to evaluate the structural basis for VEGFR-2 inhibitory activity. Some 4-aryl-1,4-dihydropyridines were synthesized in the reaction of aromatic aldehydes and ethyl propiolate with anilines in acetic acid. The biological activities were evaluated against the cells A549, A431 and Hep-G2. The results indicated that 4-aryl-1,4-dihydropyridines could be the promising potential VEGFR-2 inhibitors.
作者简介
W. Sun
College of Life Science and Bioengineering
Email: hongyan@bjut.edu.cn
中国, Pingleyuan no. 100 of Chaoyang District, Beijing, 100124
Z. Ma
College of Life Science and Bioengineering
Email: hongyan@bjut.edu.cn
中国, Pingleyuan no. 100 of Chaoyang District, 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, Pingleyuan no. 100 of Chaoyang District, Beijing, 100124