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10.1371/journal.pone.0245962

http://scihub22266oqcxt.onion/10.1371/journal.pone.0245962
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33524017!7850479!33524017
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suck abstract from ncbi


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pmid33524017      PLoS+One 2021 ; 16 (2): e0245962
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  • A drug repurposing screen identifies hepatitis C antivirals as inhibitors of the SARS-CoV2 main protease #MMPMID33524017
  • Baker JD; Uhrich RL; Kraemer GC; Love JE; Kraemer BC
  • PLoS One 2021[]; 16 (2): e0245962 PMID33524017show ga
  • Effective SARS-CoV-2 antiviral drugs are desperately needed. The SARS-CoV-2 main protease (Mpro) appears as an attractive target for drug development. We show that the existing pharmacopeia contains many drugs with potential for therapeutic repurposing as selective and potent inhibitors of SARS-CoV-2 Mpro. We screened a collection of ~6,070 drugs with a previous history of use in humans for compounds that inhibit the activity of Mpro in vitro and found ~50 compounds with activity against Mpro. Subsequent dose validation studies demonstrated 8 dose responsive hits with an IC50
  • |*Drug Evaluation, Preclinical[MESH]
  • |*Drug Repositioning[MESH]
  • |Antiviral Agents/*pharmacology/*therapeutic use[MESH]
  • |Biological Assay[MESH]
  • |Fluorescence[MESH]
  • |Hepacivirus/*drug effects[MESH]
  • |Hepatitis C/*drug therapy[MESH]
  • |High-Throughput Screening Assays[MESH]
  • |Humans[MESH]
  • |Protease Inhibitors/*pharmacology[MESH]
  • |Reproducibility of Results[MESH]


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