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About:
Potent inhibitors of SARS-CoV-2 3C-like protease derived from N-substituted isatin compounds
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Potent inhibitors of SARS-CoV-2 3C-like protease derived from N-substituted isatin compounds
Creator
Liu, Ying
Liu, Hongbo
Liu, Y
Lai, Luhua
Li, Chunmei
Liang, Hao
Li, C
Liu, Pei
Sun, Qi
Deng, X
Liu, H
Liu, P
Lai, L
Sun, Q
Deng, Xiaobing
Liang, H
Bnlms, ‖
Source
Elsevier; Medline; PMC
abstract
SARS-CoV-2 3C-like protease is the main protease of SARS-CoV-2 and has been considered as one of the key targets for drug discovery against COVID-19. We identified several N-substituted isatin compounds as potent SARS-CoV-2 3C-like protease inhibitors. The three most potent compounds inhibit SARS-CoV-2 3C-like protease with IC(50)’s of 45 nM, 47 nM and 53 nM, respectively. Our study indicates that N-substituted isatin compounds have the potential to be developed as broad-spectrum anti-coronavirus drugs.
has issue date
2020-08-01
(
xsd:dateTime
)
bibo:doi
10.1016/j.ejmech.2020.112702
bibo:pmid
32798789
has license
no-cc
sha1sum (hex)
e672db0dbc349b3c1a450d0643d5359ba20a0ea3
schema:url
https://doi.org/10.1016/j.ejmech.2020.112702
resource representing a document's title
Potent inhibitors of SARS-CoV-2 3C-like protease derived from N-substituted isatin compounds
has PubMed Central identifier
PMC7395831
has PubMed identifier
32798789
schema:publication
Eur J Med Chem
resource representing a document's body
covid:e672db0dbc349b3c1a450d0643d5359ba20a0ea3#body_text
is
schema:about
of
named entity 'isatin'
named entity 'inhibitors'
named entity 'derived'
named entity 'isatin'
named entity 'protease'
named entity 'EUROPEAN'
named entity 'Journal'
named entity 'isatin'
named entity 'European Journal of Medicinal Chemistry'
named entity 'SARS-CoV-2'
named entity '3C-like protease'
named entity 'acetic acid'
named entity 'C-5'
named entity '3CL protease'
named entity 'Hydrophobic'
named entity 'isatin'
named entity 'isatin'
named entity 'synthetic route'
named entity 'Thr'
named entity 'assay'
named entity 'enzyme assay'
named entity 'SARS-CoV-2'
named entity 'carboxylic acid'
named entity 'EtOAc'
named entity 'ester'
named entity 'proteases'
named entity 'SARS-CoV-2'
named entity 'protease'
named entity 'Melting points'
named entity 'SARS'
named entity 'H-bonds'
named entity 'carboxamide'
named entity 'synthetic route'
named entity 'SARS-CoV'
named entity 'carboxamide'
named entity 'cysteine'
named entity 'naphthalene'
named entity 'RNA genome'
named entity 'H-bonds'
named entity 'peptidomimetics'
named entity 'naphthyl group'
named entity 'isatin'
named entity 'SARS'
named entity 'SARS-CoV-2'
named entity 'amino group'
named entity 'mmol'
named entity 'acetate'
named entity 'ethanamide'
named entity 'carboxyl groups'
named entity 'SARS-CoV-2'
named entity 'nucleophile'
named entity 'RNA virus'
named entity 'isatin'
named entity 'carbon'
named entity 'methyl group'
named entity 'Tideglusib'
named entity 'Escherichia coli'
named entity 'coronavirus'
named entity '3, 4'
named entity 'SARS-CoV'
named entity 'substrate'
named entity 'synthetic peptide'
named entity 'traditional Chinese medicine'
named entity 'aromatic substitution'
named entity 'isatin'
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