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A threefold approach including quantum chemical, molecular docking and molecular dynamic studies to explore the natural compounds from Centaurea jacea as the potential inhibitors for COVID-19.
Muhammad, S; Maqbool, M F; Al-Sehemi, A G; Iqbal, A; Khan, M; Ullah, S; Khan, M T.
  • Muhammad S; King Khalid University, College of Science, Department of Physics, Abha, Saudi Arabia.
  • Maqbool MF; University of the Punjab, Department of Zoology, Quaid-e-Azam Campus, Lahore, Pakistan.
  • Al-Sehemi AG; King Khalid University, College of Science, Department of Chemistry, Abha, Saudi Arabia.
  • Iqbal A; King Khalid University, Research Center for Advanced Material Science - RCAMS, Abha, Saudi Arabia.
  • Khan M; University of Veterinary and Animal Sciences, Department of Wildlife and Ecology, Lahore, Pakistan.
  • Ullah S; University of the Punjab, Department of Zoology, Quaid-e-Azam Campus, Lahore, Pakistan.
  • Khan MT; King Khalid University, College of Science, Department of Chemistry, Abha, Saudi Arabia.
Braz J Biol ; 83: e247604, 2021.
Article in English | MEDLINE | ID: covidwho-2243538
ABSTRACT
In the current report, we studied the possible inhibitors of COVID-19 from bioactive constituents of Centaurea jacea using a threefold approach consisting of quantum chemical, molecular docking and molecular dynamic techniques. Centaurea jacea is a perennial herb often used in folk medicines of dermatological complaints and fever. Moreover, anticancer, antioxidant, antibacterial and antiviral properties of its bioactive compounds are also reported. The Mpro (Main proteases) was docked with different compounds of Centaurea jacea through molecular docking. All the studied compounds including apigenin, axillarin, Centaureidin, Cirsiliol, Eupatorin and Isokaempferide, show suitable binding affinities to the binding site of SARS-CoV-2 main protease with their binding energies -6.7 kcal/mol, -7.4 kcal/mol, -7.0 kcal/mol, -5.8 kcal/mol, -6.2 kcal/mol and -6.8 kcal/mol, respectively. Among all studied compounds, axillarin was found to have maximum inhibitor efficiency followed by Centaureidin, Isokaempferide, Apigenin, Eupatorin and Cirsiliol. Our results suggested that axillarin binds with the most crucial catalytic residues CYS145 and HIS41 of the Mpro, moreover axillarin shows 5 hydrogen bond interactions and 5 hydrophobic interactions with various residues of Mpro. Furthermore, the molecular dynamic calculations over 60 ns (6×106 femtosecond) time scale also shown significant insights into the binding effects of axillarin with Mpro of SARS-CoV-2 by imitating protein like aqueous environment. From molecular dynamic calculations, the RMSD and RMSF computations indicate the stability and dynamics of the best docked complex in aqueous environment. The ADME properties and toxicity prediction analysis of axillarin also recommended it as safe drug candidate. Further, in vivo and in vitro investigations are essential to ensure the anti SARS-CoV-2 activity of all bioactive compounds particularly axillarin to encourage preventive use of Centaurea jacea against COVID-19 infections.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pharmaceutical Preparations / Centaurea / COVID-19 Type of study: Prognostic study Topics: Traditional medicine Limits: Humans Language: English Journal: Braz J Biol Journal subject: Biology Year: 2021 Document Type: Article Affiliation country: 1519-6984.247604

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pharmaceutical Preparations / Centaurea / COVID-19 Type of study: Prognostic study Topics: Traditional medicine Limits: Humans Language: English Journal: Braz J Biol Journal subject: Biology Year: 2021 Document Type: Article Affiliation country: 1519-6984.247604