4.7 Article

Geranylated flavonoids displaying SARS-CoV papain-like protease inhibition from the fruits of Paulownia tomentosa

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 21, Issue 11, Pages 3051-3057

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2013.03.027

Keywords

SARS-CoV PLpro; Paulownia tomentosa; Geranylated flavonoids; PLpro inhibitor

Funding

  1. Bio & Medical Technology Development Program of the National Research Foundation (NRF)
  2. government (MEST) [20110002235]
  3. BK21 program
  4. Howard Hughes Medical Institute International Predoctoral Fellowship
  5. National Research Foundation of Korea [2013M3A9A6003180] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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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