Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery

Recently, Dai W et al. published a study on Science,1 in which the two lead compounds 11a and 11b were designed and synthesized based on the features of a key enzyme Mpro of SARSCoV-2 (Fig. 1). In particular, compound 11a is a potential drug candidate for coronavirus disease 2019 (COVID-19) with str...

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Autores:
Tipo de recurso:
Article of investigation
Fecha de publicación:
2020
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
Repositorio:
Expeditio: repositorio UTadeo
Idioma:
eng
OAI Identifier:
oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/14043
Acceso en línea:
https://doi.org/10.1038/s41392-020-00291-8
http://hdl.handle.net/20.500.12010/14043
Palabra clave:
Targeting Mpro
Anti SARS-CoV-2
Drug discovery
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
Rights
License
Abierto (Texto Completo)
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oai_identifier_str oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/14043
network_acronym_str UTADEO2
network_name_str Expeditio: repositorio UTadeo
repository_id_str
dc.title.spa.fl_str_mv Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
title Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
spellingShingle Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
Targeting Mpro
Anti SARS-CoV-2
Drug discovery
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
title_short Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
title_full Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
title_fullStr Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
title_full_unstemmed Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
title_sort Promising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discovery
dc.subject.spa.fl_str_mv Targeting Mpro
Anti SARS-CoV-2
Drug discovery
topic Targeting Mpro
Anti SARS-CoV-2
Drug discovery
Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
dc.subject.lemb.spa.fl_str_mv Síndrome respiratorio agudo grave
COVID-19
SARS-CoV-2
Coronavirus
description Recently, Dai W et al. published a study on Science,1 in which the two lead compounds 11a and 11b were designed and synthesized based on the features of a key enzyme Mpro of SARSCoV-2 (Fig. 1). In particular, compound 11a is a potential drug candidate for coronavirus disease 2019 (COVID-19) with strong anti-SARS-CoV-2 infection activity, good pharmacokinetics characteristics, and low toxicity. Since December 2019, the outbreak of COVID-19 caused by SARS-CoV-22 has caused a serious global public health emergency. So far, the global epidemic is still in the outbreak stage, and the number of new confirmed cases every day has exceeded 100,000 for several days. At present, the main drugs used clinically include interferon-alpha, lopinavir/ritonavir, ribavirin, arbidol, etc. However, these drugs are facing huge controversy due to the large side effects or the lack of clinical verifications of the therapeutic effects.3 Therefore, clarifying the origin and pathogenesis of pneumonia and decoding the key targets against SARS-CoV-2 are the cornerstone to design and discover safe and effective antivirus drugs.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-09-30T20:43:14Z
dc.date.available.none.fl_str_mv 2020-09-30T20:43:14Z
dc.date.created.none.fl_str_mv 2020
dc.type.local.spa.fl_str_mv Artículo
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
format http://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.issn.spa.fl_str_mv 2059-3635
dc.identifier.other.spa.fl_str_mv https://doi.org/10.1038/s41392-020-00291-8
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/14043
dc.identifier.doi.spa.fl_str_mv https://doi.org/10.1038/s41392-020-00291-8
identifier_str_mv 2059-3635
url https://doi.org/10.1038/s41392-020-00291-8
http://hdl.handle.net/20.500.12010/14043
dc.language.iso.spa.fl_str_mv eng
language eng
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.local.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.extent.spa.fl_str_mv 2 páginas
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Signal Transduction and Targeted Therapy
dc.source.spa.fl_str_mv reponame:Expeditio Repositorio Institucional UJTL
instname:Universidad de Bogotá Jorge Tadeo Lozano
instname_str Universidad de Bogotá Jorge Tadeo Lozano
institution Universidad de Bogotá Jorge Tadeo Lozano
reponame_str Expeditio Repositorio Institucional UJTL
collection Expeditio Repositorio Institucional UJTL
bitstream.url.fl_str_mv https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/14043/2/license.txt
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spelling 2020-09-30T20:43:14Z2020-09-30T20:43:14Z20202059-3635https://doi.org/10.1038/s41392-020-00291-8http://hdl.handle.net/20.500.12010/14043https://doi.org/10.1038/s41392-020-00291-8Recently, Dai W et al. published a study on Science,1 in which the two lead compounds 11a and 11b were designed and synthesized based on the features of a key enzyme Mpro of SARSCoV-2 (Fig. 1). In particular, compound 11a is a potential drug candidate for coronavirus disease 2019 (COVID-19) with strong anti-SARS-CoV-2 infection activity, good pharmacokinetics characteristics, and low toxicity. Since December 2019, the outbreak of COVID-19 caused by SARS-CoV-22 has caused a serious global public health emergency. So far, the global epidemic is still in the outbreak stage, and the number of new confirmed cases every day has exceeded 100,000 for several days. At present, the main drugs used clinically include interferon-alpha, lopinavir/ritonavir, ribavirin, arbidol, etc. However, these drugs are facing huge controversy due to the large side effects or the lack of clinical verifications of the therapeutic effects.3 Therefore, clarifying the origin and pathogenesis of pneumonia and decoding the key targets against SARS-CoV-2 are the cornerstone to design and discover safe and effective antivirus drugs.2 páginasapplication/pdfengSignal Transduction and Targeted Therapyreponame:Expeditio Repositorio Institucional UJTLinstname:Universidad de Bogotá Jorge Tadeo LozanoTargeting MproAnti SARS-CoV-2Drug discoverySíndrome respiratorio agudo graveCOVID-19SARS-CoV-2CoronavirusPromising inhibitors targeting Mpro: an ideal strategy for anti- SARS-CoV-2 drug discoveryArtículohttp://purl.org/coar/resource_type/c_2df8fbb1Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Chen, YiWang, GuanOuyang, LiangLICENSElicense.txtlicense.txttext/plain; charset=utf-82938https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/14043/2/license.txtabceeb1c943c50d3343516f9dbfc110fMD52open accessTHUMBNAILs41392-020-00291-8.pdf.jpgs41392-020-00291-8.pdf.jpgIM Thumbnailimage/jpeg24016https://expeditiorepositorio.utadeo.edu.co/bitstream/20.500.12010/14043/3/s41392-020-00291-8.pdf.jpg2746a6779450b0bfce3933b055970868MD53open access20.500.12010/14043oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/140432021-03-17 19:49:14.674metadata only accessRepositorio Institucional - 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