Volume 23, Issue 3 (8-2021)                   yafte 2021, 23(3): 106-118 | Back to browse issues page

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Rafieyanbroujeni M, Rezaeinasab R. Molecular Docking of Some Quinazolinone Analogues as an EGFR Inhibitors. yafte. 2021; 23 (3) :106-118
URL: http://yafte.lums.ac.ir/article-1-3084-en.html
Department of Medicinal Chemistry, Faculty of Pharmacy, Lorestan, University of Medical Sciences, Khorramabad, Iran
Abstract:   (154 Views)
Background: Mutations that cause high expression of epidermal growth factor can lead to cancer. Therefore, this factor serves as a potential molecular target for cancer treatment, and inhibitors of this enzyme are of particular importance in the treatment of cancer. This study aimed to investigate the bioinformatics of inhibition of EGFR enzyme by a number of quinazolinone derivatives.
Materials and Methods: This study was conducted based on a descriptive-analytical method. To investigate how quinazolinone derivatives bind to the active site of the enzyme, the chemical structure of the compounds was first plotted using ChemBioDrawUltra software (version 14). It was then transferred to Hyperchem software for energy optimization. Docking studies were performed using AutoDock software (version 4.2), and in the final stage, the results were analyzed using three programs, including AutoDockTools, DS Visualizer, and Ligplot.
Results: Based on the results of docking studies, the most important bonds involved in drug-receptor binding are hydrophobic and hydrogen bonds. Among all the studied compounds, the best docking results are related to compound number 3. This compound with the most negative binding energy level (ΔGbind=-7.53 Kcal/mol) has a greater tendency to bind to key amino acids at the active site of the EGFR.
Conclusion: In the end, due to the high effectiveness and docking results, it can be conclude that compound number 3 can be considered an effective erlotinib EGFR inhibitor.
Full-Text [PDF 607 kb]   (56 Downloads)    
Type of Study: Research |
Received: 2020/09/22 | Accepted: 2021/04/18 | Published: 2021/09/5

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