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Cited 198 time in webofscience Cited 227 time in scopus
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Geranylated flavonoids displaying SARS-CoV papain-like protease inhibition from the fruits of Paulownia tomentosaopen access

Authors
Cho, Jung KeunCurtis-Long, Marcus J.Lee, Kon HoKim, Dae WookRyu, Hyung WonYuk, Heung JooPark, Ki Hun
Issue Date
1-Jun-2013
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
SARS-CoV PLpro; Paulownia tomentosa; Geranylated flavonoids; PLpro inhibitor
Citation
BIOORGANIC & MEDICINAL CHEMISTRY, v.21, no.11, pp 3051 - 3057
Pages
7
Indexed
SCI
SCIE
SCOPUS
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY
Volume
21
Number
11
Start Page
3051
End Page
3057
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/20625
DOI
10.1016/j.bmc.2013.03.027
ISSN
0968-0896
1464-3391
Abstract
SARS-CoV papain-like protease (PLpro) is an important antiviral target due to its key roles in SARS virus replication. The MeOH extracts of the fruits of the Paulownia tree yielded many small molecules capable of targeting PLpro. Five of these compounds were new geranylated flavonoids, tomentin A, tomentin B, tomentin C, tomentin D, tomentin E (1-5). Structure analysis of new compounds (1-5) by NMR showed that they all contain a 3,4-dihydro-2H-pyran moiety. This chemotype is very rare and is derived from cyclization of a geranyl group with a phenol functionality. Most compounds (1-12) inhibited PLpro in a dose dependent manner with IC50's raging between 5.0 and 14.4 mu M. All new compounds having the dihydro-2H-pyran group showed better inhibition than their parent compounds (1 vs 11, 2 vs 9, 4 vs 12, 5 vs 6). In kinetic studies, 1-12 emerged to be reversible, mixed inhibitors. (C) 2013 Elsevier Ltd. All rights reserved.
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