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Integrated Chemoinformatics-Molecular Docking Approach to Drug Discovery Against Viruses.

Authors
  • Anwar, Muhammad Faraz1
  • Khalid, Ramsha2
  • Hasanain, Alina3
  • Naeem, Sadaf2
  • Zarina, Shamshad1
  • Abidi, Syed Hani4
  • Ali, Syed5
  • 1 National Center for Proteomics, University of Karachi, Karachi. Pakistan. , (Pakistan)
  • 2 Department of Biochemistry, University of Karachi, Karachi. Pakistan. , (Pakistan)
  • 3 Medical College, Aga Khan University, Karachi. Pakistan. , (Pakistan)
  • 4 Department of Biological and Biomedical Sciences, Aga Khan University, Karachi. Pakistan. , (Pakistan)
  • 5 Department of Biomedical Sciences, Nazarbayev University School of Medicine, Nazarbayev University, Astana. Kazakhstan. , (Kazakhstan)
Type
Published Article
Journal
Infectious disorders drug targets
Publication Date
Oct 19, 2018
Identifiers
DOI: 10.2174/1871526518666181019162359
PMID: 30345931
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

In the current study, we have used an integrated in silico approach that combines chemoinformatics and molecular docking to screen and test potential therapeutic compounds against viruses in a computer-simulated environment. Fluoroquinolones have been shown to inhibit HCV replication by targeting the helicase activity of HCV NS3. Based on this observation, we hypothesized that natural analogs of fluoroquinolones will have similar or superior inhibitory potential, while having potentially fewer adverse effects. To screen for natural analogs of fluoroquinolones, we devised an integrated in silico Chemoinformatics-Molecular Docking approach. Using the structural features of 17 fluoroquinolones as bait reference, we screened large databases of natural analogs. 10399 natural compounds and their derivatives were retrieved from the databases. From these compounds, molecules bearing physicochemical similarities with fluoroquinolones were screened using a chemoinformatics approach. Twenty compounds were picked up in this screening. These compounds were then docked on the structure of HCV NS3 helicase to analyze mutual interactions of the two molecules. Results from the molecular docking analysis showed 32 amino acids in the HCV NS3 active site that were most frequently targeted by fluoroquinolones as well as by their natural analogues, indicating a functional similarity between the two groups of compounds. This study describes a speedy and inexpensive approach to complement drug discovery and design. The in silico analyses we used here can be employed to short-list promising compounds prior to their testing in wet-lab. This will tremendously economize on time and money spent on the screening of putative drugs. Copyright© Bentham Science Publishers; For any queries, please email at [email protected]

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