Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Grienke, Ulrike, Braun, Heike, Seidel, Nora, Kirchmair, Johannes, Richter, Martina, Krumbholz, Andi, von Grafenstein, Susanne, Liedl, Klaus R., Schmidtke, Michaela, Rollinger, Judith M.
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
_version_ 1782309516777357312
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
work_keys_str_mv AT grienkeulrike computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT braunheike computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT seidelnora computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT kirchmairjohannes computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT richtermartina computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT krumbholzandi computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT vongrafensteinsusanne computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT liedlklausr computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT schmidtkemichaela computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents
AT rollingerjudithm computerguidedapproachtoaccesstheantiinfluenzaactivityoflicoriceconstituents