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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.bmc.2022.116814</dc:identifier><dc:language>eng</dc:language><dc:creator>Quintana, M.</dc:creator><dc:creator>Rodriguez-Rius, A.</dc:creator><dc:creator>Vellé, A.</dc:creator><dc:creator>Vives, S.</dc:creator><dc:creator>Sanz Miguel, P.J.</dc:creator><dc:creator>Triola, G.</dc:creator><dc:title>Dinuclear silver and gold bisNHC complexes as drug candidates for cancer therapy</dc:title><dc:identifier>ART-2022-128718</dc:identifier><dc:description>We report four dinuclear silver(I) and gold(I) complexes containing two different bidentate N-heterocyclic carbene ligands (bisNHC). One of these complexes 4, shows strong and selective anticancer activity against the human ovarian cancer cell line A2780. Mechanistically, 4 enhances the oxidative stress by stimulating reactive oxygen species production and inhibiting the scavenging activity of thioredoxin reductase. Our findings provide evidence that tuning ligand and electronic properties of metal-NHC complexes can modulate their reactivity and selectivity and it may result in potential novel anticancer drugs.</dc:description><dc:date>2022</dc:date><dc:source>http://zaguan.unizar.es/record/118077</dc:source><dc:doi>10.1016/j.bmc.2022.116814</dc:doi><dc:identifier>http://zaguan.unizar.es/record/118077</dc:identifier><dc:identifier>oai:zaguan.unizar.es:118077</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FSE/E42-20R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/RTI2018-096323-B-I00</dc:relation><dc:identifier.citation>Bioorganic and Medicinal Chemistry 67 (2022), 116814 [8 pp.]</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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