<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hahn F</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Wilhelm Sander-Stiftung</funding><funding>Johannes und Frieda Marohn-Stiftung</funding><pagination>E1394</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7762174</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(12)</volume><pubmed_abstract>The ongoing pandemic spread of the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) demands skillful strategies for novel drug development, drug repurposing and cotreatments, in particular focusing on existing candidates of host-directed antivirals (HDAs). The developmental drug IMU-838, currently being investigated in a phase 2b trial in patients suffering from autoimmune diseases, represents an inhibitor of human dihydroorotate dehydrogenase (DHODH) with a recently proven antiviral activity in vitro and in vivo. Here, we established an analysis system for assessing the antiviral potency of IMU-838 and DHODH-directed back-up drugs in cultured cell-based infection models. By the use of SARS-CoV-2-specific immunofluorescence, Western blot, in-cell ELISA, viral yield reducti</pubmed_abstract><journal>Viruses</journal><pubmed_title>IMU-838, a Developmental DHODH Inhibitor in Phase II for Autoimmune Disease, Shows Anti-SARS-CoV-2 and Broad-Spectrum Antiviral Efficacy In Vitro.</pubmed_title><pmcid>PMC7762174</pmcid><funding_grant_id>MA/SBT 2018.121.1</funding_grant_id><funding_grant_id>Alz/Iko-Hahn/2019</funding_grant_id><funding_grant_id>MA 1289/7-3</funding_grant_id><pubmed_authors>Hahn F</pubmed_authors><pubmed_authors>Muehler A</pubmed_authors><pubmed_authors>Uberla K</pubmed_authors><pubmed_authors>Peelen E</pubmed_authors><pubmed_authors>Dobler G</pubmed_authors><pubmed_authors>Vitt D</pubmed_authors><pubmed_authors>Hurst B</pubmed_authors><pubmed_authors>Hage S</pubmed_authors><pubmed_authors>Peter AS</pubmed_authors><pubmed_authors>Julander J</pubmed_authors><pubmed_authors>Kohlhof H</pubmed_authors><pubmed_authors>Jack HM</pubmed_authors><pubmed_authors>Ptak R</pubmed_authors><pubmed_authors>Groppel M</pubmed_authors><pubmed_authors>Fuchs J</pubmed_authors><pubmed_authors>Ruzsics Z</pubmed_authors><pubmed_authors>Marschall M</pubmed_authors><pubmed_authors>Wangen C</pubmed_authors></additional><is_claimable>false</is_claimable><name>IMU-838, a Developmental DHODH Inhibitor in Phase II for Autoimmune Disease, Shows Anti-SARS-CoV-2 and Broad-Spectrum Antiviral Efficacy In Vitro.</name><description>The ongoing pandemic spread of the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) demands skillful strategies for novel drug development, drug repurposing and cotreatments, in particular focusing on existing candidates of host-directed antivirals (HDAs). The developmental drug IMU-838, currently being investigated in a phase 2b trial in patients suffering from autoimmune diseases, represents an inhibitor of human dihydroorotate dehydrogenase (DHODH) with a recently proven antiviral activity in vitro and in vivo. Here, we established an analysis system for assessing the antiviral potency of IMU-838 and DHODH-directed back-up drugs in cultured cell-based infection models. By the use of SARS-CoV-2-specific immunofluorescence, Western blot, in-cell ELISA, viral yield reducti</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2026-05-02T16:58:09.232Z</modification><creation>2021-02-20T17:12:12Z</creation></dates><accession>S-EPMC7762174</accession><cross_references><pubmed>33291455</pubmed><doi>10.3390/v12121394</doi></cross_references></HashMap>