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In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro))
Momordica charintia, a well-known plant called bitter melon, has been shown to have antibacterial, anti-diabetic, and antiviral properties against HIV infection. The goal of this work was to investigate the inhibitory effect of phytocompounds found in Momordica charintia leaf extracts on SARS-CoV-2...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008047/ https://www.ncbi.nlm.nih.gov/pubmed/36935867 http://dx.doi.org/10.1016/j.imu.2023.101216 |
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author | Adedayo, Ayodeji Famuti, Ayodeji |
author_facet | Adedayo, Ayodeji Famuti, Ayodeji |
author_sort | Adedayo, Ayodeji |
collection | PubMed |
description | Momordica charintia, a well-known plant called bitter melon, has been shown to have antibacterial, anti-diabetic, and antiviral properties against HIV infection. The goal of this work was to investigate the inhibitory effect of phytocompounds found in Momordica charintia leaf extracts on SARS-CoV-2 3CL protease (also known as the Main protease, M(pro)) utilizing GC-MS analysis and molecular docking studies. The Crystal Structure of the SARS-CoV-2 3CL protease in complex with an inhibitor N3 was downloaded from RCSB using PDB ID 6LU7 with resolution: 2.16 Å. In the present study, in silico molecular docking analysis of phytoconstituents present in M. charantia methanolic leaf extract detected by GC–MS was studied against SARS-CoV-2 M(pro). The results revealed 13 phytochemical constituents derived from the GC-MS analysis. Quercetin 3-galactopyranoside, Rutin, and Hyperin were ranked the highest with binding scores ranging from −8.9 kcal/mol to −8.5 kcal/mol compared with the standard, Nirmatrelvir, with a binding score of −7.7 kcal/mol. From the results obtained, it can be concluded that Quercetin 3-galactopyranoside, Rutin, and Hyperin act against Covid-19 by inhibiting the SARS-COV-2 M(pro) and therefore can be further developed into potent drugs for Covid-19 treatment. |
format | Online Article Text |
id | pubmed-10008047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100080472023-03-13 In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) Adedayo, Ayodeji Famuti, Ayodeji Inform Med Unlocked Article Momordica charintia, a well-known plant called bitter melon, has been shown to have antibacterial, anti-diabetic, and antiviral properties against HIV infection. The goal of this work was to investigate the inhibitory effect of phytocompounds found in Momordica charintia leaf extracts on SARS-CoV-2 3CL protease (also known as the Main protease, M(pro)) utilizing GC-MS analysis and molecular docking studies. The Crystal Structure of the SARS-CoV-2 3CL protease in complex with an inhibitor N3 was downloaded from RCSB using PDB ID 6LU7 with resolution: 2.16 Å. In the present study, in silico molecular docking analysis of phytoconstituents present in M. charantia methanolic leaf extract detected by GC–MS was studied against SARS-CoV-2 M(pro). The results revealed 13 phytochemical constituents derived from the GC-MS analysis. Quercetin 3-galactopyranoside, Rutin, and Hyperin were ranked the highest with binding scores ranging from −8.9 kcal/mol to −8.5 kcal/mol compared with the standard, Nirmatrelvir, with a binding score of −7.7 kcal/mol. From the results obtained, it can be concluded that Quercetin 3-galactopyranoside, Rutin, and Hyperin act against Covid-19 by inhibiting the SARS-COV-2 M(pro) and therefore can be further developed into potent drugs for Covid-19 treatment. Published by Elsevier Ltd. 2023 2023-03-11 /pmc/articles/PMC10008047/ /pubmed/36935867 http://dx.doi.org/10.1016/j.imu.2023.101216 Text en © 2023 Published by Elsevier Ltd. 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 Adedayo, Ayodeji Famuti, Ayodeji In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) |
title | In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) |
title_full | In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) |
title_fullStr | In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) |
title_full_unstemmed | In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) |
title_short | In-silico studies of Momordica charantia extracts as potential candidates against SARS-CoV-2 targeting human main protease enzyme (M(pro)) |
title_sort | in-silico studies of momordica charantia extracts as potential candidates against sars-cov-2 targeting human main protease enzyme (m(pro)) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008047/ https://www.ncbi.nlm.nih.gov/pubmed/36935867 http://dx.doi.org/10.1016/j.imu.2023.101216 |
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