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Computer-Guided Approach to Access the Anti-influenza Activity of Licorice Constituents
[Image: see text] 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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society and American
Society of Pharmacognosy
2013
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971757/ https://www.ncbi.nlm.nih.gov/pubmed/24313801 http://dx.doi.org/10.1021/np400817j |
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author | Grienke, Ulrike Braun, Heike Seidel, Nora Kirchmair, Johannes Richter, Martina Krumbholz, Andi von Grafenstein, Susanne Liedl, Klaus R. Schmidtke, Michaela Rollinger, Judith M. |
author_facet | Grienke, Ulrike Braun, Heike Seidel, Nora Kirchmair, Johannes Richter, Martina Krumbholz, Andi von Grafenstein, Susanne Liedl, Klaus R. Schmidtke, Michaela Rollinger, Judith M. |
author_sort | Grienke, Ulrike |
collection | PubMed |
description | [Image: see text] 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. |
format | Online Article Text |
id | pubmed-3971757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American
Chemical
Society and American
Society of Pharmacognosy |
record_format | MEDLINE/PubMed |
spelling | pubmed-39717572014-04-01 Computer-Guided Approach to Access the Anti-influenza Activity of Licorice Constituents Grienke, Ulrike Braun, Heike Seidel, Nora Kirchmair, Johannes Richter, Martina Krumbholz, Andi von Grafenstein, Susanne Liedl, Klaus R. Schmidtke, Michaela Rollinger, Judith M. J Nat Prod [Image: see text] 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. American Chemical Society and American Society of Pharmacognosy 2013-12-06 2014-03-28 /pmc/articles/PMC3971757/ /pubmed/24313801 http://dx.doi.org/10.1021/np400817j Text en Copyright © 2013 American Chemical Society and American Society of Pharmacognosy Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Grienke, Ulrike Braun, Heike Seidel, Nora Kirchmair, Johannes Richter, Martina Krumbholz, Andi von Grafenstein, Susanne Liedl, Klaus R. Schmidtke, Michaela Rollinger, Judith M. Computer-Guided Approach to Access the Anti-influenza Activity of Licorice Constituents |
title | Computer-Guided
Approach to Access the Anti-influenza
Activity of Licorice Constituents |
title_full | Computer-Guided
Approach to Access the Anti-influenza
Activity of Licorice Constituents |
title_fullStr | Computer-Guided
Approach to Access the Anti-influenza
Activity of Licorice Constituents |
title_full_unstemmed | Computer-Guided
Approach to Access the Anti-influenza
Activity of Licorice Constituents |
title_short | Computer-Guided
Approach to Access the Anti-influenza
Activity of Licorice Constituents |
title_sort | computer-guided
approach to access the anti-influenza
activity of licorice constituents |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3971757/ https://www.ncbi.nlm.nih.gov/pubmed/24313801 http://dx.doi.org/10.1021/np400817j |
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