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About:
Repurposing Pyramax®, Quinacrine and Tilorone as Treatments for Ebola Virus Disease
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schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Repurposing Pyramax®, Quinacrine and Tilorone as Treatments for Ebola Virus Disease
Creator
Holbrook, Michael
Dyall, Julie
Zhou, Huanying
Postnikova, Elena
Ekins, Sean
Liang, Janie
Lane, Thomas
Liang, E
Madrid, Peter
Zhou, C
Foil, Daniel
Goodin, Caleb
Goodin, L
Holbrook, J
Madrid, M
Mercer, J
Mercer, Luke
Pyramax®, Repurposing
Source
Elsevier; Medline; PMC
abstract
Abstract We have recently identified three molecules (tilorone, quinacrine and pyronaridine tetraphosphate) which all demonstrated efficacy in the mouse model of infection with mouse-adapted Ebola virus (EBOV) model of disease and had similar in vitro inhibition of an Ebola pseudovirus (VSV-EBOV-GP), suggesting they interfere with viral entry. Using a machine learning model to predict lysosomotropism these compounds were evaluated for their ability to possess a lysosomotropic mechanism in vitro. We now demonstrate in vitro that pyronaridine tetraphosphate is an inhibitor of Lysotracker accumulation in lysosomes (IC50 = 0.56 μM). Further, we evaluated antiviral synergy between pyronaridine and artesunate (Pyramax®), which are used in combination to treat malaria. Artesunate was not found to have lysosomotropic activity in vitro and the combination effect on EBOV inhibition was shown to be additive. Pyramax® may represent a unique example of the repurposing of a combination product for another disease.
has issue date
2020-08-13
(
xsd:dateTime
)
bibo:doi
10.1016/j.antiviral.2020.104908
bibo:pmid
32798602
has license
els-covid
sha1sum (hex)
67301f02784dc83fd22109641da4aa326f041ef5
schema:url
https://doi.org/10.1016/j.antiviral.2020.104908
resource representing a document's title
Repurposing Pyramax®, Quinacrine and Tilorone as Treatments for Ebola Virus Disease
has PubMed Central identifier
PMC7425680
has PubMed identifier
32798602
schema:publication
Antiviral Research
resource representing a document's body
covid:67301f02784dc83fd22109641da4aa326f041ef5#body_text
is
schema:about
of
named entity 'demonstrated'
named entity 'pyronaridine'
named entity 'Virus'
named entity 'Disease'
named entity 'Short'
named entity 'INHIBITION'
named entity 'Ebola'
named entity 'identified'
named entity 'chloroquine'
named entity 'infection'
named entity 'guinea pig'
named entity 'EBOV'
named entity 'antiviral'
named entity 'EBOV'
named entity 'amphiphilic'
named entity 'probability'
named entity 'tilorone'
named entity 'drug metabolism'
named entity 'artesunate'
named entity 'fetal bovine serum'
named entity 'molecule'
named entity 'Assay'
named entity 'pyronaridine'
named entity 'approved drugs'
named entity 'Git'
named entity 'lysosomal'
named entity 'ThermoFisher'
named entity 'Montreal'
named entity 'tilorone'
named entity 'Madrid'
named entity 'Vero cells'
named entity 'antivirals'
named entity 'EBOV'
named entity 'synergistic'
named entity 'EVD'
named entity 'Madrid'
named entity 'Democratic Republic of the Congo'
named entity 'Madrid'
named entity 'malaria'
named entity 'cell death'
named entity 'PBS'
named entity 'acid sphingomyelinase'
named entity 'pKa'
named entity 'artesunate'
named entity 'cholesterol'
named entity 'ATCC'
named entity 'pyronaridine'
named entity 'quinacrine'
named entity 'viral entry'
named entity 'quinacrine'
named entity 'mouse model'
named entity 'VSV-EBOV'
named entity 'treatment for Ebola'
named entity 'Quinacrine'
named entity 'EBOV'
named entity 'endosomes'
named entity 'EBOV'
named entity 'pyronaridine'
named entity 'EBOV'
named entity 'high throughput'
named entity 'quinacrine'
named entity 'correlation'
named entity 'clinical trial'
named entity 'quinacrine'
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