中文关键词:流感病毒小分子抑制剂Nucleozin构效关系 英文关键词:influenza virussmall molecular inhibitorsNucleozinstructure-activity relationship 基金项目:

作者	单位	E-mail
燕子红	喀什大学化学与环境科学学院 喀什844006	172761175@qq.com
蔡岩	南开大学 化学学院元素有机化学国家重点实验室 天津300071
丁晓丽	a喀什大学化学与环境科学学院 喀什844006
苗志伟	南开大学化学学院

摘要点击次数:1439 全文下载次数:0 中文摘要: 小分子化合物Nucleozin作为靶向流感病毒核蛋白的抑制剂具有良好的抑制活性，本文围绕Nucleozin分子中与哌嗪环直接相连的芳环部分进行研究，通过钯催化偶联反应合成了一系列Nucleozin衍生物，通过检测所合成化合物对流感病毒H1N1的抑制活性，明确了Nucleozin分子中该部分的构效关系。利用甲基在药物分子设计中的作用，设计将分子中的氯原子替换为甲基，研究发现与原型分子Nucleozin相比其抑制活性有了明显的提高，对该类分子成药性的提高具有积极意义。 英文摘要: Nucleozin has good inhibitory activity as an inhibitor against influenza virus nucleoprotein. In this paper, we investigate the aromatic ring part which is connected directly with piperazine in the Nucleozin molecular structure. A series of Nucleozin derivatives has been synthesized by palladium catalyzed coupling reaction, and the structure-activity relationship of this part in Nucleozin molecule is clarified by detecting the inhibitory activities of the synthesized compounds on influenza virus H1N1. Furthermore, using the role of methyl group in the design of drug molecules, the design of the chlorine atom in the molecule was replaced by a methyl group. It was found that the inhibitory activity was significantly improved compared with the prototype molecule Nucleozin. This study has a significant meaning in the drug-like improvement of this kind of molecular. 查看全文查看/发表评论下载PDF阅读器 相关附件：附件1版权转让声明书 -->