Pterocarpans and flavanones from Sophora flavescens displaying potent neuraminidase inhibition

被引:102
作者
Ryu, Young Bae [1 ,2 ]
Curtis-Long, Marcus J.
Kim, Jin Hyo [2 ]
Jeong, Seong Hun [2 ]
Yang, Min Suk [2 ]
Lee, Keun Woo [2 ]
Lee, Woo Song [1 ]
Park, Ki Hun [2 ]
机构
[1] KRIBB, Bioind Res Ctr, Jeongeup 580185, South Korea
[2] Gyeongsang Natl Univ, Grad Sch, Inst Agr & Life Sci, Div Appl Life Sci,Program BK21,EB NCRC, Jinju 660701, South Korea
关键词
Neuraminidase; Pterocarpan; Sophora flavescens;
D O I
10.1016/j.bmcl.2008.10.033
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
Pterocarpans (1-3) and flavanones (4-10) were isolated from Sophora flavescens and screened for their ability to inhibit neuraminidase (an enzyme crucial in the proliferation of the influenza virus). The majority of inhibitors were shown to have IC50 values of 20 mu M or below. Interestingly, pterocarpan 1 emerged as the best inhibitor with an IC50 of 1.4 mu M. We were thus able to prove that the pterocarpan skeleton is a new class of lead structure for neuraminidase inhibitors. Our studies reveal that the IC50 has a marked dependence upon structure in the case of the pterocarpans but much less so for the flavanones. Kinetic analysis disclosed that all inhibitors are noncompetitive. Our molecular docking experiment resulted that the most potent pterocarpan-derived inhibitor 1 may bind to another binding pocket adjacent to the active site. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6046 / 6049
页数:4
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