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About:
Several FDA-approved drugs effectively inhibit SARS-CoV-2 infection in vitro
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
associated with source
document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
Attributes
Values
type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Several FDA-approved drugs effectively inhibit SARS-CoV-2 infection in vitro
Creator
Zhang, Jun
Yang, Yang
Ma, Jian
Yuan, Quan
Ge, Sheng-Xiang
Xia, Ning-Shao
Cao, Jia-Li
Qiao, Xiao-Yang
Shen, Chen-Guang
Shi, Tian-Shu
Xiong, Hua-Long
Zhang, Tian-Ying
Source
BioRxiv
abstract
To identify drugs that are potentially used for the treatment of COVID-19, the potency of 1403 FDA-approved drugs were evaluated using a robust pseudovirus assay and the candidates were further confirmed by authentic SARS-CoV-2 assay. Four compounds, Clomiphene (citrate), Vortioxetine, Vortioxetine (hydrobromide) and Asenapine (hydrochloride), showed potent inhibitory effects in both pseudovirus and authentic virus assay. The combination of Clomiphene (citrate), Vortioxetine and Asenapine (hydrochloride) is much more potent than used alone, with IC50 of 0.34 μM.
has issue date
2020-06-05
(
xsd:dateTime
)
bibo:doi
10.1101/2020.06.05.135996
has license
biorxiv
sha1sum (hex)
fb921a8d4534a3693e061acc58444e75fa04275d
schema:url
https://doi.org/10.1101/2020.06.05.135996
resource representing a document's title
Several FDA-approved drugs effectively inhibit SARS-CoV-2 infection in vitro
schema:publication
bioRxiv
resource representing a document's body
covid:fb921a8d4534a3693e061acc58444e75fa04275d#body_text
is
schema:about
of
named entity 'Vortioxetine'
named entity 'Clomiphene'
named entity 'SARS-CoV-2'
named entity 'FDA'
named entity 'COVID-19'
named entity 'The combination'
named entity 'potent'
named entity 'infection'
named entity 'pseudovirus'
named entity 'SARS-CoV-2 virus'
named entity 'Amiodarone'
named entity 'combination therapy'
named entity 'non-linear regression'
named entity 'VSV'
named entity 'genome'
named entity 'IC50'
named entity 'pseudovirus'
named entity 'citrate'
named entity 'Asenapine'
named entity 'half maximal inhibitory concentration'
named entity 'SARS-CoV-2'
named entity 'Vortioxetine'
named entity 'Vortioxetine'
named entity 'COVID-19'
named entity 'Clomiphene'
named entity 'Vortioxetine'
named entity 'hydrochloride'
named entity 'assay'
named entity 'virus'
named entity 'IC50'
named entity 'hydrochloride'
named entity 'citrate'
named entity 'FDA'
named entity 'potency'
named entity 'FDA'
named entity 'SARS-CoV-2'
named entity 'pseudovirus'
named entity 'Chloroquine'
named entity 'Clomifene'
named entity 'pharmacological'
named entity 'virus'
named entity 'COVID'
named entity 'fluorescence'
named entity 'infection'
named entity 'schizophrenia'
named entity 'bipolar I disorder'
named entity 'SARS-CoV-2'
named entity 'agonist'
named entity 'VSV'
named entity 'citrate'
named entity 'combination therapies'
named entity 'clinical evaluation'
named entity 'infection'
named entity 'virus infection'
named entity 'SARS-CoV-2'
named entity 'infection'
named entity 'spike protein'
named entity 'prophylaxis'
named entity 'Chloroquine'
named entity 'virus'
named entity 'cytopathic effect'
named entity 'citrate'
named entity 'SARS-CoV-2'
named entity 'virus'
named entity 'antiviral drug'
named entity 'SARS-CoV-2'
named entity 'Vortioxetine'
named entity 'pseudovirus'
named entity 'cytotoxicity'
named entity 'vesicular stomatitis virus'
named entity 'chloride'
named entity 'virtual screening'
named entity 'SARS-CoV-2'
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