Volume 25, Issue 3 (Autumn 2021)                   2021, 25(3): 161-168 | Back to browse issues page

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Piri H, Hajialilo E, Hashemi Ghermezi S N, Taghi Goodarzi M, Salemi-Bazargani S, Eghdami A. Quantitative Structure-Activity Relationships and Molecular Docking Simulation of Allicin Compounds as Inhibitors of COVID-19 Protease Enzyme. Journal of Inflammatory Diseases. 2021; 25 (3) :161-168
URL: http://journal.qums.ac.ir/article-1-3257-en.html
1- Department of Biochemistry & Genetics, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
2- Department of Parasitology and Mycology, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
3- Department of Industrial Engineering, Faculty of Engineering, Saveh Branch, Islamic Azad University, Saveh, Iran.
4- Department of Biochemistry, Islamic Azad University, Shahrood Branch, Shahrood, Iran.
5- Student Research Committee, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
6- Department of Biochemistry, School of Medicine, Saveh Branch, Islamic Azad University, Saveh, Iran. , eghdami49@gmail.com
Abstract:   (538 Views)
Background: Coronavirus (CoV) is a group of viruses that cause disease in humans and animals. These viruses contain crown-shaped spike glycoproteins on their surface.
Objective: We conducted a quantitative structure-activity relationship (QSAR) study on a series of 36 compounds of allicin to assess their antiviral activities against the main protease of COVID-19.
Methods: In the present descriptive-analytic study, the information on the structure of compounds, the COVID-19 protease enzyme, and the Allicin derivatives was obtained from the databases such as the Research Collaboratory for Structural Bioinformatics’ Protein Data Bank (PDB) and PubChem. The QSAR method, analysis of correlations and multiple linear regressions were carried out. Six molecular descriptors such as constitutional and molecular topology descriptors were selected for the model. Finally, molecular docking was performed in iGEMDOCK 2.1 software.
Results: The obtained multi-parametric model reported a correlation coefficient of about 0.89, indicating that the model was able to satisfactory predict the antiviral activity of allicin compounds.
Conclusion: The findings obtained can be valuable in designing, synthesizing, and developing novel antiviral agents with allicin-based scaffold.
Article number: 4
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Type of Study: Research | Subject: Biochemistry

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