Novel Therapeutics Directed to COVID-19 RNA Targets

Grant number: unknown

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Key facts

  • Disease

    COVID-19
  • Funder

    University of Minnesota
  • Principal Investigator

    PhD. Kathleen Boris-Lawrie
  • Research Location

    United States of America
  • Lead Research Institution

    College of Veterinary Medicine, University of Minnesota
  • Research Priority Alignment

    N/A
  • Research Category

    Therapeutics research, development and implementation

  • Research Subcategory

    Pre-clinical studies

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

This study will produce lead compounds that inhibit the synthesis of SARS-CoV2 viral proteins and attenuate SARS-CoV2 transmission. In this study researchers will: Employ FDA-approved compounds and optimized small molecules with affinity and specificity for RNA targets. Apply cell-based and future biophysical screening tools to identify molecules with specificity to SARS-CoV2 RNA without cellular toxicity. This research will identify small molecule inhibitors of SARS-CoV2 RNA. The 5' end of all SARS-CoV2 RNAs is identical and highly conserved. This 65 nucleotide sequence has an integral role in the viral replication cycle. In preliminary studies, researchers have identified RNA-biased small molecules binding the 5' end of HIV RNA at concentrations within the range of compounds in clinical trials. The effect of these compounds on HIV replication was documented. The compounds reduced virion production and diminished sentinel replication intermediates. Here researchers will employ the validated viral screening assay to identify compounds binding the SARS-CoV2 RNA and deregulating SARS-CoV2 RNA function.