Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12722
Title: Several coumarin derivatives and their Pd(ii) complexes as potential inhibitors of the main protease of SARS-CoV-2, anin silicoapproach
Authors: Milenkovic, Dejan
Dimic, Dusan
Avdović, Edina
Marković, Zoran
Journal: RSC Advances
Issue Date: 23-Sep-2020
Abstract: © The Royal Society of Chemistry 2020. The global pandemic of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) caused many fatalities among people and significantly influenced the global economy. Since efficient treatment is not available, the computational methods in biology and chemistry are a promising starting point towards adequate medication. Three previously synthesized coumarin derivatives and their Pd(ii) complexes were examined for the binding affinity towards the Mproprotein of SARS-CoV-2 by molecular docking and compared to two Food and Drug Administration (FDA) drugs,cinanserinandchloroquine. All of the investigated compounds bind to the active position of the mentioned protein. Coumarin-Pd(ii) complexes showed higher binding affinities compared to the approved drugs. The bindings of the bis(3-(1-((3-chlorophenyl)amino)ethylidene)-chroman-2,4-dione) palladium(ii) complex, its corresponding ligand, andcinanserinto SARS-CoV-2 Mprowere further subjected to the molecular dynamics simulations. The binding free energies, computed by MM/PBSA approach were analyzed in detail and the importance of specific interactions outlined. These results showed that the molecules bearing structural similarity to the approved drugs and their complexes have the potential to inhibit the functional activity of SARS-CoV-2 protease and further experimental studies should be undertaken.
URI: https://scidar.kg.ac.rs/handle/123456789/12722
Type: Article
DOI: 10.1039/d0ra07062a
SCOPUS: 85092592073
Appears in Collections:Institute for Information Technologies, Kragujevac
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