Novel Therapeutics Directed to COVID-19 RNA Targets
- Funded by University of Minnesota
- Total publications:0 publications
Grant number: unknown
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Key facts
Disease
COVID-19Funder
University of MinnesotaPrincipal Investigator
PhD. Kathleen Boris-LawrieResearch Location
United States of AmericaLead Research Institution
College of Veterinary Medicine, University of MinnesotaResearch 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.