<i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches

Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can result in severe damage to the respiratory system. With no specific treatment to date, it is crucial to identify potent inhibitors of SARS-CoV-2 Chymotrypsin-like protease (3CLpro) that could also modulate the enz...

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Main Authors: Ana-Maria Udrea, Maria Mernea, Cătălin Buiu, Speranța Avram
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Processes
Subjects:
Online Access:https://www.mdpi.com/2227-9717/8/11/1468
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spelling doaj-da90106b400a44168f35a9564ba84e5e2020-11-25T04:11:11ZengMDPI AGProcesses2227-97172020-11-0181468146810.3390/pr8111468<i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology ApproachesAna-Maria Udrea0Maria Mernea1Cătălin Buiu2Speranța Avram3Department of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 91–95 Splaiul Independenţei, 050095 Bucharest, RomaniaDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 91–95 Splaiul Independenţei, 050095 Bucharest, RomaniaDepartment of Automatic Control and Systems Engineering, Politehnica University of Bucharest, 313 Splaiul Independenţei, 060042 Bucharest, RomaniaDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 91–95 Splaiul Independenţei, 050095 Bucharest, RomaniaBackground: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can result in severe damage to the respiratory system. With no specific treatment to date, it is crucial to identify potent inhibitors of SARS-CoV-2 Chymotrypsin-like protease (3CLpro) that could also modulate the enzymes involved in the respiratory damage that accompanies SARS-CoV-2 infection. Here, flavones isolated from <i>Scutellaria baicalensis</i> (baicalein, baicalin, wogonin, norwogonin, and oroxylin A) were studied as possible compounds in the treatment of SARS-CoV-2 and SARS-CoV-2-induced acute lung injuries. Methods: We used structural bioinformatics and cheminformatics to (i) identify the critical molecular features of flavones for their binding activity at human and SARS-CoV-2 enzymes; (ii) predict their drug-likeness and leader-likeness features; (iii) calculate their pharmacokinetic profile, with an emphasis on toxicology; (iv) predict their pharmacodynamic profiles, with the identification of their human body targets involved in the respiratory system injuries; and (v) dock the ligands to SARS-CoV-2 3CLpro. Results: All flavones presented appropriate drug-like and kinetics features, except for baicalin. Flavones could bind to SARS-CoV-2 3CLpro at a similar site, but interact slightly differently with the protease. Flavones’ pharmacodynamic profiles predict that (i) wogonin strongly binds at the cyclooxygenase2 and nitric oxide synthase; (ii) baicalein and norwogonin could modulate lysine-specific demethylase 4D-like and arachidonate 15-lipoxygenase; and (iii) baicalein, wogonin, norwogonin, and oroxylin A bind to SARS-CoV-2 3CLpro. Conclusions: Our results propose these flavones as possible potent drugs against respiratory damage that occurs during SARS-CoV-2 infections, with a strong recommendation for baicalein.https://www.mdpi.com/2227-9717/8/11/1468infectionsantiviralflavonoidspharmacokineticspharmacodynamicSARS-CoV-2
collection DOAJ
language English
format Article
sources DOAJ
author Ana-Maria Udrea
Maria Mernea
Cătălin Buiu
Speranța Avram
spellingShingle Ana-Maria Udrea
Maria Mernea
Cătălin Buiu
Speranța Avram
<i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches
Processes
infections
antiviral
flavonoids
pharmacokinetics
pharmacodynamic
SARS-CoV-2
author_facet Ana-Maria Udrea
Maria Mernea
Cătălin Buiu
Speranța Avram
author_sort Ana-Maria Udrea
title <i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches
title_short <i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches
title_full <i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches
title_fullStr <i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches
title_full_unstemmed <i>Scutellaria baicalensis</i> Flavones as Potent Drugs against Acute Respiratory Injury during SARS-CoV-2 Infection: Structural Biology Approaches
title_sort <i>scutellaria baicalensis</i> flavones as potent drugs against acute respiratory injury during sars-cov-2 infection: structural biology approaches
publisher MDPI AG
series Processes
issn 2227-9717
publishDate 2020-11-01
description Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can result in severe damage to the respiratory system. With no specific treatment to date, it is crucial to identify potent inhibitors of SARS-CoV-2 Chymotrypsin-like protease (3CLpro) that could also modulate the enzymes involved in the respiratory damage that accompanies SARS-CoV-2 infection. Here, flavones isolated from <i>Scutellaria baicalensis</i> (baicalein, baicalin, wogonin, norwogonin, and oroxylin A) were studied as possible compounds in the treatment of SARS-CoV-2 and SARS-CoV-2-induced acute lung injuries. Methods: We used structural bioinformatics and cheminformatics to (i) identify the critical molecular features of flavones for their binding activity at human and SARS-CoV-2 enzymes; (ii) predict their drug-likeness and leader-likeness features; (iii) calculate their pharmacokinetic profile, with an emphasis on toxicology; (iv) predict their pharmacodynamic profiles, with the identification of their human body targets involved in the respiratory system injuries; and (v) dock the ligands to SARS-CoV-2 3CLpro. Results: All flavones presented appropriate drug-like and kinetics features, except for baicalin. Flavones could bind to SARS-CoV-2 3CLpro at a similar site, but interact slightly differently with the protease. Flavones’ pharmacodynamic profiles predict that (i) wogonin strongly binds at the cyclooxygenase2 and nitric oxide synthase; (ii) baicalein and norwogonin could modulate lysine-specific demethylase 4D-like and arachidonate 15-lipoxygenase; and (iii) baicalein, wogonin, norwogonin, and oroxylin A bind to SARS-CoV-2 3CLpro. Conclusions: Our results propose these flavones as possible potent drugs against respiratory damage that occurs during SARS-CoV-2 infections, with a strong recommendation for baicalein.
topic infections
antiviral
flavonoids
pharmacokinetics
pharmacodynamic
SARS-CoV-2
url https://www.mdpi.com/2227-9717/8/11/1468
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