Molecules2016,Vol.21Issue(8) :21.DOI:10.3390/molecules21081012

Design, Synthesis and Biological Evaluation of Benzohydrazide Derivatives Containing Dihydropyrazoles as Potential EGFR Kinase Inhibitors

Wang, Hai-Chao Yan, Xiao-Qiang Yan, Tian-Long Li, Hong-Xia Wang, Zhong-Chang Zhu, Hai-Liang
Molecules2016,Vol.21Issue(8) :21.DOI:10.3390/molecules21081012

Design, Synthesis and Biological Evaluation of Benzohydrazide Derivatives Containing Dihydropyrazoles as Potential EGFR Kinase Inhibitors

Wang, Hai-Chao 1Yan, Xiao-Qiang 2Yan, Tian-Long 2Li, Hong-Xia 1Wang, Zhong-Chang 2Zhu, Hai-Liang2
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作者信息

  • 1. Suzhou Univ, Coll Biol & Food Engn, Suzhou 234000, Peoples R China
  • 2. Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
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Abstract

A series of novel benzohydrazide derivatives containing dihydropyrazoles have been synthesized as potential epidermal growth factor receptor (EGFR) kinase inhibitors and their biological activities as potential antiproliferative agents have been evaluated. Among these compounds, compound H20 exhibited the most potent antiproliferative activity against four cancer cell line variants (A549, MCF-7, HeLa, HepG2) with IC50 values of 0.46, 0.29, 0.15 and 0.21 mu M respectively, which showed the most potent EGFR inhibition activities (IC50 = 0.08 mu M for EGFR). Molecular modeling simulation studies were performed in order to predict the biological activity and activity relationship (SAR) of these benzohydrazide derivatives. These results suggested that compound H20 may be a promising anticancer agent.

Key words

benzohydrazide derivatives/EGFR inhibitor/antiproliferative activity/cytotoxicity/molecular docking

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出版年

2016
Molecules

Molecules

SCI
ISSN:1420-3049
被引量7
参考文献量33
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