Cargando…

Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)

BACKGROUND: Since the World Health Organization (WHO) declared Coronavirus disease 2019 (COVID-19) to be a pandemic infection, important severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) non-structural proteins (nsp) have been analysed as promising targets in virtual screening approaches....

Descripción completa

Detalles Bibliográficos
Autores principales: da Silva, Felipe Moura A, da Silva, Katia Pacheco A, de Oliveira, Luiz Paulo M, Costa, Emmanoel V, Koolen, Hector HF, Pinheiro, Maria Lúcia B, de Souza, Antonia Queiroz L, de Souza, Afonso Duarte L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534957/
https://www.ncbi.nlm.nih.gov/pubmed/33027419
http://dx.doi.org/10.1590/0074-02760200207
_version_ 1783590387705708544
author da Silva, Felipe Moura A
da Silva, Katia Pacheco A
de Oliveira, Luiz Paulo M
Costa, Emmanoel V
Koolen, Hector HF
Pinheiro, Maria Lúcia B
de Souza, Antonia Queiroz L
de Souza, Afonso Duarte L
author_facet da Silva, Felipe Moura A
da Silva, Katia Pacheco A
de Oliveira, Luiz Paulo M
Costa, Emmanoel V
Koolen, Hector HF
Pinheiro, Maria Lúcia B
de Souza, Antonia Queiroz L
de Souza, Afonso Duarte L
author_sort da Silva, Felipe Moura A
collection PubMed
description BACKGROUND: Since the World Health Organization (WHO) declared Coronavirus disease 2019 (COVID-19) to be a pandemic infection, important severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) non-structural proteins (nsp) have been analysed as promising targets in virtual screening approaches. Among these proteins, 3-chymotrypsin-like cysteine protease (3CLpro), also named main protease, and the RNA-dependent RNA polymerase (RdRp), have been identified as fundamental targets due to its importance in the viral replication stages. OBJECTIVES: To investigate, in silico, two of the most abundant flavonoid glycosides from Dysphania ambrosioides; a medicinal plant found in many regions of the world, along with some of the putative derivatives of these flavonoid glycosides in the human organism as potential inhibitors of the SARS-CoV-2 3CLpro and RdRp. METHODS: Using a molecular docking approach, the interactions and the binding affinity with SARS-CoV-2 3CLpro and RdRp were predicted for quercetin-3-O-rutinoside (rutin), kaempferol-3-O-rutinoside (nicotiflorin) and some of their glucuronide and sulfate derivatives. FINDINGS: Docking analysis, based on the crystal structure of 3CLpro and RdRp, indicated rutin, nicotiflorin, and their glucuronide and sulfate derivatives as potential inhibitors for both proteins. Also, the importance of the hydrogen bond and π-based interactions was evidenced for the presumed active sites. MAIN CONCLUSIONS: Overall, these results suggest that both flavonoid glycosides and their putative human metabolites can play a key role as inhibitors of the SARS-CoV-2 3CLpro and RdRp. Obviously, further researches, mainly in vitro and in vivo experiments, are necessary to certify the docking results reported here, as well as the adequate application of these substances. Furthermore, it is necessary to investigate the risks of D. ambrosioides as a phytomedicine for use against COVID-19.
format Online
Article
Text
id pubmed-7534957
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Instituto Oswaldo Cruz, Ministério da Saúde
record_format MEDLINE/PubMed
spelling pubmed-75349572020-10-14 Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp) da Silva, Felipe Moura A da Silva, Katia Pacheco A de Oliveira, Luiz Paulo M Costa, Emmanoel V Koolen, Hector HF Pinheiro, Maria Lúcia B de Souza, Antonia Queiroz L de Souza, Afonso Duarte L Mem Inst Oswaldo Cruz Original Article BACKGROUND: Since the World Health Organization (WHO) declared Coronavirus disease 2019 (COVID-19) to be a pandemic infection, important severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) non-structural proteins (nsp) have been analysed as promising targets in virtual screening approaches. Among these proteins, 3-chymotrypsin-like cysteine protease (3CLpro), also named main protease, and the RNA-dependent RNA polymerase (RdRp), have been identified as fundamental targets due to its importance in the viral replication stages. OBJECTIVES: To investigate, in silico, two of the most abundant flavonoid glycosides from Dysphania ambrosioides; a medicinal plant found in many regions of the world, along with some of the putative derivatives of these flavonoid glycosides in the human organism as potential inhibitors of the SARS-CoV-2 3CLpro and RdRp. METHODS: Using a molecular docking approach, the interactions and the binding affinity with SARS-CoV-2 3CLpro and RdRp were predicted for quercetin-3-O-rutinoside (rutin), kaempferol-3-O-rutinoside (nicotiflorin) and some of their glucuronide and sulfate derivatives. FINDINGS: Docking analysis, based on the crystal structure of 3CLpro and RdRp, indicated rutin, nicotiflorin, and their glucuronide and sulfate derivatives as potential inhibitors for both proteins. Also, the importance of the hydrogen bond and π-based interactions was evidenced for the presumed active sites. MAIN CONCLUSIONS: Overall, these results suggest that both flavonoid glycosides and their putative human metabolites can play a key role as inhibitors of the SARS-CoV-2 3CLpro and RdRp. Obviously, further researches, mainly in vitro and in vivo experiments, are necessary to certify the docking results reported here, as well as the adequate application of these substances. Furthermore, it is necessary to investigate the risks of D. ambrosioides as a phytomedicine for use against COVID-19. Instituto Oswaldo Cruz, Ministério da Saúde 2020-09-30 /pmc/articles/PMC7534957/ /pubmed/33027419 http://dx.doi.org/10.1590/0074-02760200207 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Original Article
da Silva, Felipe Moura A
da Silva, Katia Pacheco A
de Oliveira, Luiz Paulo M
Costa, Emmanoel V
Koolen, Hector HF
Pinheiro, Maria Lúcia B
de Souza, Antonia Queiroz L
de Souza, Afonso Duarte L
Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)
title Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)
title_full Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)
title_fullStr Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)
title_full_unstemmed Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)
title_short Flavonoid glycosides and their putative human metabolites as potential inhibitors of the SARS-CoV-2 main protease (Mpro) and RNA-dependent RNA polymerase (RdRp)
title_sort flavonoid glycosides and their putative human metabolites as potential inhibitors of the sars-cov-2 main protease (mpro) and rna-dependent rna polymerase (rdrp)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534957/
https://www.ncbi.nlm.nih.gov/pubmed/33027419
http://dx.doi.org/10.1590/0074-02760200207
work_keys_str_mv AT dasilvafelipemouraa flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT dasilvakatiapachecoa flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT deoliveiraluizpaulom flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT costaemmanoelv flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT koolenhectorhf flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT pinheiromarialuciab flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT desouzaantoniaqueirozl flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp
AT desouzaafonsoduartel flavonoidglycosidesandtheirputativehumanmetabolitesaspotentialinhibitorsofthesarscov2mainproteasemproandrnadependentrnapolymeraserdrp