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Computer-Guided Approach to Access the Anti-influenza Activity of Licorice Constituents

  • Ulrike Grienke
  • , Heike Braun
  • , Nora Seidel
  • , Johannes Kirchmair
  • , Martina Richter
  • , Andi Krumbholz
  • , Susanne von Grafenstein
  • , Klaus R. Liedl
  • , Michaela Schmidtke
  • , Judith M. Rollinger

Publications: Contribution to journalArticlePeer Reviewed

Abstract

Neuraminidase (NA), a key enzyme in viral replication, is the first-line drug target to combat influenza. On the basis of a shape-focused virtual screening, the roots of Glycyrrhiza glabra (licorice) were identified as plant species with an accumulation of constituents that show 3D similarities to known influenza NA inhibitors (NAIs). Phytochemical investigation revealed 12 constituents identified as (E)-1-[2,4-dihydroxy-3-(3-methyl-2-butenyl)phenyl]-3- (8-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-2-propen-1-one (1), 3,4-dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b′]dipyran-3-ol (2), biochanin B (3), glabrol (4), glabrone (5), hispaglabridin B (6), licoflavone B (7), licorice glycoside B (8), licorice glycoside E (9), liquiritigenin (10), liquiritin (11), and prunin (12). Eleven of these constituents showed significant influenza virus NA inhibition in a chemiluminescence (CL)-based assay. Additional tests, including (i) a cell-based cytopathic effect inhibition assay (general antiviral activity), (ii) the evaluation of cytotoxicity, (iii) the inhibition of the NA of Clostridium perfringens (CL- and fluorescence (FL)-based assay), and (iv) the determination of self-fluorescence and quenching, provided further perspective on their anti-influenza virus potential, revealing possible assay interference problems and false-positive results. Compounds 1, 3, 5, and 6 showed antiviral activity, most likely caused by the inhibition of NA. Of these, compounds 1, 3, and 6 were highly ranked in shape-focused virtual screening.

Original languageEnglish
Pages (from-to)563-570
Number of pages8
JournalJournal of Natural Products
Volume77
Issue number3
DOIs
Publication statusPublished - Mar 2014
Externally publishedYes

Funding

The authors thank E. P. Ellmerer (Institute of Organic Chemistry, University of Innsbruck) for NMR measurements, B. Jahn (Department of Virology and Antiviral Therapy, Jena University Hospital) for technical assistance, K. M. Getzner and M. E. Koch (Institute of Pharmacy/Pharmacognosy, Center for Molecular Biosciences Innsbruck, University of Innsbruck) for assistance in phytochemical processing, and J. E. Fuchs (Institute of General, Inorganic and Theoretical Chemistry, Center for Molecular Biosciences Innsbruck) for discussion of computational aspects. This work was supported by the Austrian Science Fund (FWF: P24587 and P23051) and the European Social Fund (ESF and TMWAT Project 2011 FGR 0137).

Austrian Fields of Science 2012

  • 104013 Natural product chemistry

Keywords

  • INFLUENZA-VIRUS NEURAMINIDASE
  • CHEMICAL-ANALYSIS
  • HERBAL MEDICINE
  • DRUG DESIGN
  • IN-VITRO
  • A H1N1
  • FLAVONOIDS
  • IDENTIFICATION
  • RESISTANCE
  • INHIBITORS

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