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Pterocarpans and flavanones from Sophora flavescens displaying potent neuraminidase inhibition

Authors
Ryu, Young BaeCurtis-Long, Marcus J.Kim, Jin HyoJeong, Seong HunYang, Min SukLee, Keun WooLee, Woo SongPark, Ki Hun
Issue Date
1-Dec-2008
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Neuraminidase; Pterocarpan; Sophora flavescens
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.18, no.23, pp 6046 - 6049
Pages
4
Indexed
SCIE
SCOPUS
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume
18
Number
23
Start Page
6046
End Page
6049
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/27184
DOI
10.1016/j.bmcl.2008.10.033
ISSN
0960-894X
1464-3405
Abstract
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.
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