<HashMap><database>biostudies-literature</database><scores/><additional><submitter>van Niekerk A</submitter><funding>Swiss National Science Foundation</funding><funding>University of Queensland</funding><funding>Wellcome Trust</funding><funding>Australian Research Council</funding><pagination>e202300247</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10947176</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(19)</volume><pubmed_abstract>Infections associated with antimicrobial resistance (AMR) are poised to become the leading cause of death in the next few decades, a scenario that can be ascribed to two phenomena: antibiotic over-prescription and a lack of antibiotic drug development. The crowd-sourced initiative Community for Open Antimicrobial Drug Discovery (CO-ADD) has been testing research compounds contributed by researchers around the world to find new antimicrobials to combat AMR, and during this campaign has found that metallodrugs might be a promising, yet untapped source. To this end, we submitted 18 Pd&lt;sup>II&lt;/sup> - and Ru&lt;sup>II&lt;/sup> -pyridyl-1,2,3-triazolyl complexes that were developed as catalysts to assess their antimicrobial properties. It was found that the Pd complexes, especially Pd1, possessed potent antifungal activity with MICs between 0.06 and 0.125 μg mL&lt;sup>-1&lt;/sup> against Candida glabrata. The in-vitro studies were extended to in-vivo studies in Galleria mellonella larvae, where it was established that the compounds were nontoxic. Here, we effectively demonstrate the potential of Pd&lt;sup>II&lt;/sup> -pyta complexes as antifungal agents.</pubmed_abstract><journal>Chembiochem : a European journal of chemical biology</journal><pubmed_title>The Antimicrobial Properties of Pd&lt;sup>II&lt;/sup> - and Ru&lt;sup>II&lt;/sup> -pyta Complexes.</pubmed_title><pmcid>PMC10947176</pmcid><funding_grant_id>104797/Z/14/Z</funding_grant_id><funding_grant_id>FT220100152</funding_grant_id><funding_grant_id>177997</funding_grant_id><pubmed_authors>Elliott AG</pubmed_authors><pubmed_authors>Kavanagh A</pubmed_authors><pubmed_authors>Dinh H</pubmed_authors><pubmed_authors>Mapolie SF</pubmed_authors><pubmed_authors>Zuegg J</pubmed_authors><pubmed_authors>Cain AK</pubmed_authors><pubmed_authors>Frei A</pubmed_authors><pubmed_authors>Blaskovich MAT</pubmed_authors><pubmed_authors>van Niekerk A</pubmed_authors><pubmed_authors>Joseph MC</pubmed_authors><pubmed_authors>Swarts AJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Antimicrobial Properties of Pd&lt;sup>II&lt;/sup> - and Ru&lt;sup>II&lt;/sup> -pyta Complexes.</name><description>Infections associated with antimicrobial resistance (AMR) are poised to become the leading cause of death in the next few decades, a scenario that can be ascribed to two phenomena: antibiotic over-prescription and a lack of antibiotic drug development. The crowd-sourced initiative Community for Open Antimicrobial Drug Discovery (CO-ADD) has been testing research compounds contributed by researchers around the world to find new antimicrobials to combat AMR, and during this campaign has found that metallodrugs might be a promising, yet untapped source. To this end, we submitted 18 Pd&lt;sup>II&lt;/sup> - and Ru&lt;sup>II&lt;/sup> -pyridyl-1,2,3-triazolyl complexes that were developed as catalysts to assess their antimicrobial properties. It was found that the Pd complexes, especially Pd1, possessed potent antifungal activity with MICs between 0.06 and 0.125 μg mL&lt;sup>-1&lt;/sup> against Candida glabrata. The in-vitro studies were extended to in-vivo studies in Galleria mellonella larvae, where it was established that the compounds were nontoxic. Here, we effectively demonstrate the potential of Pd&lt;sup>II&lt;/sup> -pyta complexes as antifungal agents.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2026-06-29T03:18:58.603Z</modification><creation>2025-05-18T12:54:24.742Z</creation></dates><accession>S-EPMC10947176</accession><cross_references><pubmed>37593808</pubmed><doi>10.1002/cbic.202300247</doi></cross_references></HashMap>