<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim JH</submitter><funding>National Institute of Horticultural and Herbal Scienses, RDA</funding><pagination>2242704</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10405751</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(1)</volume><pubmed_abstract>Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). 3CLpro is a key enzyme in coronavirus proliferation and a treatment target for COVID-19. &lt;i>In vitro&lt;/i> and &lt;i>in silico&lt;/i>, compounds &lt;b>1&lt;/b>-&lt;b>3&lt;/b> from &lt;i>Glycyrrhiza uralensis&lt;/i> had inhibitory activity and binding affinity for 3CLpro. These compounds decreased HCoV-OC43 cytotoxicity in RD cells. Moreover, they inhibited viral growth by reducing the amounts of the necessary proteins (M, N, and RDRP). Therefore, compounds &lt;b>1&lt;/b>-&lt;b>3&lt;/b> are inhibitors of 3CLpro and HCoV-OC43 proliferation.</pubmed_abstract><journal>Journal of enzyme inhibition and medicinal chemistry</journal><pubmed_title>Inhibition by components of &lt;i>Glycyrrhiza uralensis&lt;/i> of 3CLpro and HCoV-OC43 proliferation.</pubmed_title><pmcid>PMC10405751</pmcid><funding_grant_id>PJ016777032023</funding_grant_id><pubmed_authors>Huh YC</pubmed_authors><pubmed_authors>Park WT</pubmed_authors><pubmed_authors>Kim TI</pubmed_authors><pubmed_authors>Park J</pubmed_authors><pubmed_authors>Park YI</pubmed_authors><pubmed_authors>Moon YH</pubmed_authors><pubmed_authors>Kim JH</pubmed_authors><pubmed_authors>Kang MH</pubmed_authors><pubmed_authors>Cho CW</pubmed_authors><pubmed_authors>Kang JS</pubmed_authors><pubmed_authors>Hur M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inhibition by components of &lt;i>Glycyrrhiza uralensis&lt;/i> of 3CLpro and HCoV-OC43 proliferation.</name><description>Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). 3CLpro is a key enzyme in coronavirus proliferation and a treatment target for COVID-19. &lt;i>In vitro&lt;/i> and &lt;i>in silico&lt;/i>, compounds &lt;b>1&lt;/b>-&lt;b>3&lt;/b> from &lt;i>Glycyrrhiza uralensis&lt;/i> had inhibitory activity and binding affinity for 3CLpro. These compounds decreased HCoV-OC43 cytotoxicity in RD cells. Moreover, they inhibited viral growth by reducing the amounts of the necessary proteins (M, N, and RDRP). Therefore, compounds &lt;b>1&lt;/b>-&lt;b>3&lt;/b> are inhibitors of 3CLpro and HCoV-OC43 proliferation.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2026-05-29T10:23:26.611Z</modification><creation>2025-04-04T20:01:01.409Z</creation></dates><accession>S-EPMC10405751</accession><cross_references><pubmed>37537881</pubmed><doi>10.1080/14756366.2023.2242704</doi></cross_references></HashMap>