<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li H</submitter><funding>NIDCR NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><pagination>3303-3313</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8958665</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(12)</volume><pubmed_abstract>Multidrug-resistant bacterial infections have become a global threat. We recently disclosed that the known IKK-β inhibitor IMD-0354 and subsequent analogues abrogate colistin resistance in several Gram-negative strains. Herein, we report the activity of a second-generation library of IMD-0354 analogues incorporating a benzimidazole moiety as an amide isostere. We identified several analogues that show increased colistin potentiation activity against Gram-negative bacteria.</pubmed_abstract><journal>ACS infectious diseases</journal><pubmed_title>Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants.</pubmed_title><pmcid>PMC8958665</pmcid><funding_grant_id>R01 AI136904</funding_grant_id><funding_grant_id>R01 AI104895</funding_grant_id><funding_grant_id>RO1AI136904</funding_grant_id><funding_grant_id>RO1AI104895</funding_grant_id><funding_grant_id>R01 DE022350</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Melander RJ</pubmed_authors><pubmed_authors>Ernst RK</pubmed_authors><pubmed_authors>Smith R</pubmed_authors><pubmed_authors>Jania LA</pubmed_authors><pubmed_authors>Koller BH</pubmed_authors><pubmed_authors>Melander C</pubmed_authors><pubmed_authors>Mattingly AE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Benzimidazole Isosteres of Salicylanilides Are Highly Active Colistin Adjuvants.</name><description>Multidrug-resistant bacterial infections have become a global threat. We recently disclosed that the known IKK-β inhibitor IMD-0354 and subsequent analogues abrogate colistin resistance in several Gram-negative strains. Herein, we report the activity of a second-generation library of IMD-0354 analogues incorporating a benzimidazole moiety as an amide isostere. We identified several analogues that show increased colistin potentiation activity against Gram-negative bacteria.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-04-05T12:52:53.361Z</modification><creation>2025-04-05T12:52:53.361Z</creation></dates><accession>S-EPMC8958665</accession><cross_references><pubmed>34752055</pubmed><doi>10.1021/acsinfecdis.1c00463</doi></cross_references></HashMap>