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Targeting natural products against SARS-CoV-2

The human coronavirus disease (COVID-19) pandemic is caused by a novel coronavirus; the Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2). Natural products, secondary metabolites show positive leads with antiviral and immunotherapy treatments using genomic studies in silico docking. In addi...

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Autores principales: Al-Harrasi, Ahmed, Behl, Tapan, Upadhyay, Tanuj, Chigurupati, Sridevi, Bhatt, Shvetank, Sehgal, Aayush, Bhatia, Saurabh, Singh, Sukhbir, Sharma, Neelam, Vijayabalan, Shantini, Palanimuthu, Vasanth Raj, Das, Suprava, Kaur, Rajwinder, Aleya, Lotfi, Bungau, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972763/
https://www.ncbi.nlm.nih.gov/pubmed/35362883
http://dx.doi.org/10.1007/s11356-022-19770-2
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author Al-Harrasi, Ahmed
Behl, Tapan
Upadhyay, Tanuj
Chigurupati, Sridevi
Bhatt, Shvetank
Sehgal, Aayush
Bhatia, Saurabh
Singh, Sukhbir
Sharma, Neelam
Vijayabalan, Shantini
Palanimuthu, Vasanth Raj
Das, Suprava
Kaur, Rajwinder
Aleya, Lotfi
Bungau, Simona
author_facet Al-Harrasi, Ahmed
Behl, Tapan
Upadhyay, Tanuj
Chigurupati, Sridevi
Bhatt, Shvetank
Sehgal, Aayush
Bhatia, Saurabh
Singh, Sukhbir
Sharma, Neelam
Vijayabalan, Shantini
Palanimuthu, Vasanth Raj
Das, Suprava
Kaur, Rajwinder
Aleya, Lotfi
Bungau, Simona
author_sort Al-Harrasi, Ahmed
collection PubMed
description The human coronavirus disease (COVID-19) pandemic is caused by a novel coronavirus; the Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2). Natural products, secondary metabolites show positive leads with antiviral and immunotherapy treatments using genomic studies in silico docking. In addition, it includes the action of a mechanism targeting the SARS-CoV-2. In this literature, we aimed to evaluate the antiviral movement of the NT-VRL-1 unique terpene definition to Human coronavirus (HCoV-229E). The effects of 19 hydrolysable tannins on the SARS-CoV-2 were therefore theoretically reviewed and analyzed utilising the molecular operating surroundings for their C-Like protease 3CLpro catalytic dyad residues Angiotensin converting enzyme-2 (MOE 09). Pedunculagin, tercatan, and castalin were detected as interacting strongly with SARS-receptor Cov-2’s binding site and catalytic dyad (Cys145 and His41). SARS-CoV-2 methods of subunit S1 (ACE2) inhibit the interaction of the receiver with the s-protein once a drug molecule is coupled to the s-protein and prevent it from infecting the target cells in alkaloids. Our review strongly demonstrates the evidence that natural compounds and their derivatives can be used against the human coronavirus and serves as an area of research for future perspective.
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spelling pubmed-89727632022-04-01 Targeting natural products against SARS-CoV-2 Al-Harrasi, Ahmed Behl, Tapan Upadhyay, Tanuj Chigurupati, Sridevi Bhatt, Shvetank Sehgal, Aayush Bhatia, Saurabh Singh, Sukhbir Sharma, Neelam Vijayabalan, Shantini Palanimuthu, Vasanth Raj Das, Suprava Kaur, Rajwinder Aleya, Lotfi Bungau, Simona Environ Sci Pollut Res Int Review Article The human coronavirus disease (COVID-19) pandemic is caused by a novel coronavirus; the Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2). Natural products, secondary metabolites show positive leads with antiviral and immunotherapy treatments using genomic studies in silico docking. In addition, it includes the action of a mechanism targeting the SARS-CoV-2. In this literature, we aimed to evaluate the antiviral movement of the NT-VRL-1 unique terpene definition to Human coronavirus (HCoV-229E). The effects of 19 hydrolysable tannins on the SARS-CoV-2 were therefore theoretically reviewed and analyzed utilising the molecular operating surroundings for their C-Like protease 3CLpro catalytic dyad residues Angiotensin converting enzyme-2 (MOE 09). Pedunculagin, tercatan, and castalin were detected as interacting strongly with SARS-receptor Cov-2’s binding site and catalytic dyad (Cys145 and His41). SARS-CoV-2 methods of subunit S1 (ACE2) inhibit the interaction of the receiver with the s-protein once a drug molecule is coupled to the s-protein and prevent it from infecting the target cells in alkaloids. Our review strongly demonstrates the evidence that natural compounds and their derivatives can be used against the human coronavirus and serves as an area of research for future perspective. Springer Berlin Heidelberg 2022-04-01 2022 /pmc/articles/PMC8972763/ /pubmed/35362883 http://dx.doi.org/10.1007/s11356-022-19770-2 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Al-Harrasi, Ahmed
Behl, Tapan
Upadhyay, Tanuj
Chigurupati, Sridevi
Bhatt, Shvetank
Sehgal, Aayush
Bhatia, Saurabh
Singh, Sukhbir
Sharma, Neelam
Vijayabalan, Shantini
Palanimuthu, Vasanth Raj
Das, Suprava
Kaur, Rajwinder
Aleya, Lotfi
Bungau, Simona
Targeting natural products against SARS-CoV-2
title Targeting natural products against SARS-CoV-2
title_full Targeting natural products against SARS-CoV-2
title_fullStr Targeting natural products against SARS-CoV-2
title_full_unstemmed Targeting natural products against SARS-CoV-2
title_short Targeting natural products against SARS-CoV-2
title_sort targeting natural products against sars-cov-2
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8972763/
https://www.ncbi.nlm.nih.gov/pubmed/35362883
http://dx.doi.org/10.1007/s11356-022-19770-2
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