Candidate drugs against SARS-CoV-2 and COVID-19
| dc.creator | McKee, Dwight L. | |
| dc.creator | Sternberg, Ariane | |
| dc.creator | Stange, Ulrike | |
| dc.creator | Laufer, Stefan | |
| dc.creator | Naujokat, Cord | |
| dc.date.accessioned | 2020-08-24T22:18:33Z | |
| dc.date.available | 2020-08-24T22:18:33Z | |
| dc.date.created | 2020-07 | |
| dc.description.abstractenglish | Outbreak and pandemic of coronavirus SARS-CoV-2 in 2019/2020 will challenge global health for the future. Because a vaccine against the virus will not be available in the near future, we herein try to offer a pharmacological strategy to combat the virus. There exists a number of candidate drugs that may inhibit infection with and replication of SARS-CoV-2. Such drugs comprise inhibitors of TMPRSS2 serine protease and inhibitors of angiotensin-converting enzyme 2 (ACE2). Blockade of ACE2, the host cell receptor for the S protein of SARS-CoV-2 and inhibition of TMPRSS2, which is required for S protein priming may prevent cell entry of SARS-CoV-2. Further, chloroquine and hydroxychloroquine, and off-label antiviral drugs, such as the nucleotide analogue remdesivir, HIV protease inhibitors lopinavir and ritonavir, broad-spectrum antiviral drugs arbidol and favipiravir as well as antiviral phytochemicals available to date may limit spread of SARS-CoV-2 and morbidity and mortality of COVID-19 pandemic. | spa |
| dc.format.extent | 9 páginas | spa |
| dc.format.mimetype | application/pdf | spa |
| dc.identifier.doi | https://doi.org/10.1016/j.phrs.2020.104859 | spa |
| dc.identifier.issn | 1043-6618 | spa |
| dc.identifier.other | https://www.sciencedirect.com/science/article/pii/S1043661820311671?via%3Dihub | spa |
| dc.identifier.uri | https://hdl.handle.net/20.500.12010/12169 | |
| dc.language.iso | eng | spa |
| dc.publisher | Pharmacological Research | spa |
| dc.rights.accessrights | info:eu-repo/semantics/embargoedAccess | spa |
| dc.rights.local | Acceso restringido | spa |
| dc.source | reponame:Expeditio Repositorio Institucional UJTL | spa |
| dc.source | instname:Universidad de Bogotá Jorge Tadeo Lozano | spa |
| dc.subject | COVID-19 | spa |
| dc.subject.keyword | Drugs | spa |
| dc.subject.keyword | Camostat | spa |
| dc.subject.keyword | Chloroquine | spa |
| dc.subject.keyword | Remdesivir | spa |
| dc.subject.keyword | Lopinavir | spa |
| dc.subject.keyword | Ritonavir | spa |
| dc.subject.keyword | Favipiravir | spa |
| dc.subject.keyword | Arbidol | spa |
| dc.subject.keyword | Phytochemicals | spa |
| dc.subject.lemb | Síndrome respiratorio agudo grave | spa |
| dc.subject.lemb | COVID-19 | spa |
| dc.subject.lemb | SARS-CoV-2 | spa |
| dc.subject.lemb | Coronavirus | spa |
| dc.title | Candidate drugs against SARS-CoV-2 and COVID-19 | spa |
| dc.type.coar | http://purl.org/coar/resource_type/c_6501 | spa |
| dc.type.hasversion | info:eu-repo/semantics/acceptedVersion | spa |
| dc.type.local | Artículo | spa |
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