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Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?

With the gradual increase in the COVID-19 mortality rate, there is an urgent need for an effective drug/vaccine. Several drugs like Remdesivir, Azithromycin, Favirapir, Ritonavir, Darunavir, etc., are put under evaluation in more than 300 clinical trials to treat COVID-19. On the other hand, several...

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Autores principales: Saha, Sovan, Halder, Anup Kumar, Bandyopadhyay, Soumyendu Sekhar, Chatterjee, Piyali, Nasipuri, Mita, Bose, Debdas, Basu, Subhadip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390099/
https://www.ncbi.nlm.nih.gov/pubmed/34455072
http://dx.doi.org/10.1016/j.ymeth.2021.08.007
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author Saha, Sovan
Halder, Anup Kumar
Bandyopadhyay, Soumyendu Sekhar
Chatterjee, Piyali
Nasipuri, Mita
Bose, Debdas
Basu, Subhadip
author_facet Saha, Sovan
Halder, Anup Kumar
Bandyopadhyay, Soumyendu Sekhar
Chatterjee, Piyali
Nasipuri, Mita
Bose, Debdas
Basu, Subhadip
author_sort Saha, Sovan
collection PubMed
description With the gradual increase in the COVID-19 mortality rate, there is an urgent need for an effective drug/vaccine. Several drugs like Remdesivir, Azithromycin, Favirapir, Ritonavir, Darunavir, etc., are put under evaluation in more than 300 clinical trials to treat COVID-19. On the other hand, several vaccines like Pfizer-BioNTech, Moderna, Johnson & Johnson’s Janssen, Sputnik V, Covishield, Covaxin, etc., also evolved from the research study. While few of them already gets approved, others show encouraging results and are still under assessment. In parallel, there are also significant developments in new drug development. But, since the approval of new molecules takes substantial time, drug repurposing studies have also gained considerable momentum. The primary agent of the disease progression of COVID-19 is SARS-CoV2/nCoV, which is believed to have ~89% genetic resemblance with SARS-CoV, a coronavirus responsible for the massive outbreak in 2003. With this hypothesis, Human-SARS-CoV protein interactions are used to develop an in-silico Human-nCoV network by identifying potential COVID-19 human spreader proteins by applying the SIS model and fuzzy thresholding by a possible COVID-19 FDA drugs target-based validation. At first, the complete list of FDA drugs is identified for the level-1 and level-2 spreader proteins in this network, followed by applying a drug consensus scoring strategy. The same consensus strategy is involved in the second analysis but on a curated overlapping set of key genes/proteins identified from COVID-19 symptoms. Validation using subsequent docking study has also been performed on COVID-19 potential drugs with the available major COVID-19 crystal structures whose PDB IDs are: 6LU7, 6M2Q, 6W9C, 6M0J, 6M71 and 6VXX. Our computational study and docking results suggest that Fostamatinib (R406 as its active promoiety) may also be considered as one of the potential candidates for further clinical trials in pursuit to counter the spread of COVID-19.
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spelling pubmed-83900992021-08-27 Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate? Saha, Sovan Halder, Anup Kumar Bandyopadhyay, Soumyendu Sekhar Chatterjee, Piyali Nasipuri, Mita Bose, Debdas Basu, Subhadip Methods Article With the gradual increase in the COVID-19 mortality rate, there is an urgent need for an effective drug/vaccine. Several drugs like Remdesivir, Azithromycin, Favirapir, Ritonavir, Darunavir, etc., are put under evaluation in more than 300 clinical trials to treat COVID-19. On the other hand, several vaccines like Pfizer-BioNTech, Moderna, Johnson & Johnson’s Janssen, Sputnik V, Covishield, Covaxin, etc., also evolved from the research study. While few of them already gets approved, others show encouraging results and are still under assessment. In parallel, there are also significant developments in new drug development. But, since the approval of new molecules takes substantial time, drug repurposing studies have also gained considerable momentum. The primary agent of the disease progression of COVID-19 is SARS-CoV2/nCoV, which is believed to have ~89% genetic resemblance with SARS-CoV, a coronavirus responsible for the massive outbreak in 2003. With this hypothesis, Human-SARS-CoV protein interactions are used to develop an in-silico Human-nCoV network by identifying potential COVID-19 human spreader proteins by applying the SIS model and fuzzy thresholding by a possible COVID-19 FDA drugs target-based validation. At first, the complete list of FDA drugs is identified for the level-1 and level-2 spreader proteins in this network, followed by applying a drug consensus scoring strategy. The same consensus strategy is involved in the second analysis but on a curated overlapping set of key genes/proteins identified from COVID-19 symptoms. Validation using subsequent docking study has also been performed on COVID-19 potential drugs with the available major COVID-19 crystal structures whose PDB IDs are: 6LU7, 6M2Q, 6W9C, 6M0J, 6M71 and 6VXX. Our computational study and docking results suggest that Fostamatinib (R406 as its active promoiety) may also be considered as one of the potential candidates for further clinical trials in pursuit to counter the spread of COVID-19. Elsevier Inc. 2022-07 2021-08-27 /pmc/articles/PMC8390099/ /pubmed/34455072 http://dx.doi.org/10.1016/j.ymeth.2021.08.007 Text en © 2021 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Saha, Sovan
Halder, Anup Kumar
Bandyopadhyay, Soumyendu Sekhar
Chatterjee, Piyali
Nasipuri, Mita
Bose, Debdas
Basu, Subhadip
Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?
title Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?
title_full Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?
title_fullStr Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?
title_full_unstemmed Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?
title_short Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?
title_sort drug repurposing for covid-19 using computational screening: is fostamatinib/r406 a potential candidate?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390099/
https://www.ncbi.nlm.nih.gov/pubmed/34455072
http://dx.doi.org/10.1016/j.ymeth.2021.08.007
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