E
Eunhee Kim
Researcher at Chosun University
Publications - 13
Citations - 310
Eunhee Kim is an academic researcher from Chosun University. The author has contributed to research in topics: Neuraminidase & Neuraminidase inhibitor. The author has an hindex of 5, co-authored 13 publications receiving 264 citations. Previous affiliations of Eunhee Kim include Chungnam National University.
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Chalcones as novel influenza A (H1N1) neuraminidase inhibitors from Glycyrrhiza inflata.
TL;DR: Evidence of synergistic effect makes this inhibitor to have a potential possibility for control of pandemic infection by oseltamivir-resistant influenza virus.
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C-Methylated Flavonoids from Cleistocalyx operculatus and Their Inhibitory Effects on Novel Influenza A (H1N1) Neuraminidase
Trong Tuan Dao,Bui-Thanh Tung,Phi Hung Nguyen,Phuong Thien Thuong,Sung-Sik Yoo,Eunhee Kim,Sang Kyum Kim,Won Keun Oh +7 more
TL;DR: Results indicate that C-methylated flavonoids from C. operculatus have the potential to be developed as neuraminidase inhibitors for novel influenza H1N1.
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Xanthones from Polygala karensium inhibit neuraminidases from influenza A viruses.
TL;DR: The results suggest that xanthones from P. karensium may be useful in the prevention and treatment of disease by influenza viruses.
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Influenza A (H1N1) neuraminidase inhibitors from Vitis amurensis
Thi Ngoc Anh Nguyen,Trong Tuan Dao,Bui Thanh Tung,Hwan-won Choi,Eunhee Kim,Junsoo Park,Seong Il Lim,Won Keun Oh +7 more
TL;DR: Eight oligostilbenes isolated as active principles from the methanol extract of Vitis amurensis showed synergistic effect of a combination of these non-competitive inhibitors with oseltamivir makes them a potential possibility for the control of influenza infections.
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Three new coumarins from Saposhnikovia divaricata and their porcine epidemic diarrhea virus (PEDV) inhibitory activity.
TL;DR: Quantitative real-time PCR data showed inhibitory effect of 5 on genes responsible for synthesis of PEDV vital structural proteins (GP6 nucleocapsid, GP2 spike, and GP5 membrane) in a dose-dependent manner, which represents a new class of chemical entities for developing anti-PEDV agents.