标题:Caffeic acid derivatives: A new type of influenza neuraminidase inhibitors
作者:Xie,Y.;Huang,B.;Yu,K.;Shi,F.;Liu,T.;Xu,W.
作者机构:[Xie, Y] Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Shandong University, 44 West Culture Road, Jinan, Shandong 250012, Chin 更多
通讯作者:Xu, WF
通讯作者地址:[Xu, WF]Shandong Univ, Sch Pharmaceut Sci, Dept Med Chem, 44 West Culture Rd, Jinan 250012, Shandong, Peoples R China.
来源:Bioorganic and Medicinal Chemistry Letters
出版年:2013
卷:23
期:12
页码:3556-3560
DOI:10.1016/j.bmcl.2013.04.033
关键词:Amino acid;Caffeic acid;Influenza;Neuraminidase
摘要:Recently, many natural products, especially some plant-derived polyphenols have been found to exert antiviral effects against influenza virus and show inhibitory activities on neuraminidases (NAs). In our research, we took caffeic acid which contained two phenolic hydroxyl groups as the basic fragment to build a small compound library with various structures. The enzyme inhibition result indicated that some compounds exhibited moderate activities against NA and compound 15d was the best with IC50 = 7.2 μM and 8.5 μM against N2 and N1 NAs, respectively. The 3,4-dihydroxyphenyl group from caffeic acid was important for the activity according to the docking analysis. Besides, compound 15d was found to be a non-competitive inhibitor with Ki = 11.5 ± 0.25 μM by the kinetic study and also presented anti-influenza virus activity in chicken embryo fibroblast cells. It seemed promising to discover more potent NA inhibitors from caffeic acid derivatives to cope with influenza virus.
收录类别:SCOPUS;SCIE
WOS核心被引频次:23
Scopus被引频次:24
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84878110144&doi=10.1016%2fj.bmcl.2013.04.033&partnerID=40&md5=f930884b3bc585eb709608c5bd61ec61
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