[Design, synthesis and evaluation of a novel MEK protein inhibitors].

药学学报 Pub Date : 2017-03-01
Bin-bin Song, Zi-kuo Zhang, Qing-feng Zhu, Gu He, Ju-zheng Fan
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引用次数: 0

Abstract

This study was conducted to design and synthetize highly efficient, specific, non-resistant small MEK inhibitors. Based on active small molecules which have been reported, we studied the action mode with MEK protein using Autodock 4.2, generated innovative and feasible design method, designed novel small MEK protein inhibitors with a reference to molecular modeling and docking. The anti-tumor activities of four kinds of cells including MCF-7, PANC-1, SY5Y, A549 were tested with MTT method in vitro. The structure of 10 new small molecules has been determined with 1H NMR and 13C NMR. The compounds 4, 6, 7, 8, 10 had high antitumor activities, the compounds 1, 3, 5 also showed good activity, and the compounds 2, 9 showed cell selectivity in killing tumor.

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一种新型MEK蛋白抑制剂的设计、合成和评价
本研究旨在设计和合成高效、特异性、非耐药的小MEK抑制剂。基于已有报道的活性小分子,利用Autodock 4.2研究其与MEK蛋白的作用模式,生成创新可行的设计方法,参考分子建模与对接设计出新型的MEK蛋白小分子抑制剂。采用MTT法检测MCF-7、PANC-1、SY5Y、A549四种细胞的体外抗肿瘤活性。用1H NMR和13C NMR测定了10个新小分子的结构。化合物4、6、7、8、10具有较高的抗肿瘤活性,化合物1、3、5也具有较好的抗肿瘤活性,化合物2、9具有细胞选择性杀伤肿瘤。
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来源期刊
药学学报
药学学报 Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.20
自引率
0.00%
发文量
0
期刊介绍: Acta Pharmaceutica Sinica B (APSB) is a bimonthly English peer-reviewed online journal in ScienceDirect, which publishes significant original research articles, communications and high quality reviews of recent advances. APSB encourages submissions from all areas of pharmaceutical sciences, including pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis and pharmacokinetics. APSB is a part of the series Acta Pharmaceutica Sinica, which was founded in 1953. The journal is co-published by Elsevier B.V., in association with the Institute of MateriaMedica, Chinese Academy of Medical Sciences and Chinese Pharmaceutical Association.
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