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Raloxifene and Bazedoxifene Could Be Promising Candidates for Preventing the COVID-19 Related Cytokine Storm, ARDS and Mortality
K. Smetana, D. Rosel, J. Brábek,
Language English Country Greece
Document type Journal Article
NLK
Free Medical Journals
from 2004 to 2 years ago
PubMed Central
from 2017
Europe PubMed Central
from 2017
Open Access Digital Library
from 2004-01-01
PubMed
32871847
DOI
10.21873/invivo.12135
Knihovny.cz E-resources
- MeSH
- Betacoronavirus drug effects pathogenicity MeSH
- Cytokines antagonists & inhibitors genetics MeSH
- Indoles pharmacology MeSH
- Interleukin-6 antagonists & inhibitors genetics MeSH
- Coronavirus Infections drug therapy genetics mortality virology MeSH
- Humans MeSH
- Pandemics MeSH
- Raloxifene Hydrochloride pharmacology MeSH
- Receptors, Estrogen antagonists & inhibitors MeSH
- Selective Estrogen Receptor Modulators pharmacology MeSH
- Signal Transduction drug effects MeSH
- Respiratory Distress Syndrome drug therapy prevention & control virology MeSH
- Pneumonia, Viral drug therapy genetics mortality virology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
The FDA-approved drugs raloxifene and bazedoxifene could be among the best candidates to prevent mortality in severe COVID-19 patients. Raloxifene and bazedoxifene inhibit IL-6 signaling at therapeutic doses, suggesting they have the potential to prevent the cytokine storm, ARDS and mortality in severe COVID-19 patients, as is being shown with humanized antibodies blocking IL-6 signaling. In addition, raloxifene and bazedoxifene are selective estrogen receptor modulators with strong antiviral activity.
References provided by Crossref.org
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