<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Bernhard Ellinger</submitter><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD29</full_dataset_link><repository>bioimages</repository><additional_accession>http://idr.openmicroscopy.org/webclient/?show=screen-2603</additional_accession><figure_sub>Organization</figure_sub><figure_sub>Screen A</figure_sub><figure_sub>Protocol</figure_sub><figure_sub>Screen B</figure_sub><pubmed_authors>Bernhard Ellinger</pubmed_authors></additional><is_claimable>false</is_claimable><name>SARS-COV-2 drug repurposing - Caco2 cell line</name><description>To identify possible candidates for progression towards clinical studies against SARS-CoV-2, we screened a well-defined collection of 5632 compounds including 3488 compounds which have undergone clinical investigations (marketed drugs, phases 1 -3, and withdrawn) across 600 indications. Compounds were screened for their inhibition of viral induced cytotoxicity using the human epithelial colorectal adenocarcinoma cell line Caco-2 and a SARS-CoV-2 isolate. The primary screen of 5632 compounds gave 271 hits. A total of 64 compounds with IC50 &lt;20 μM were identified, including 19 compounds with IC50 &lt; 1 μM. Of this confirmed hit population, 90% have not yet been previously reported as active against SARS-CoV-2 in-vitro cell assays. Some 37 of the actives are launched drugs, 19 are in phases 1-3</description><dates><release>2020-10-08T00:00:00Z</release><modification>2023-08-21T07:40:51.803Z</modification><creation>2020-10-02T11:24:10Z</creation></dates><accession>S-BIAD29</accession><cross_references/></HashMap>