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dc.contributor.authorMadzivire, C.R.
dc.contributor.authorCarames-Mendez, P.
dc.contributor.authorPask, C.M.
dc.contributor.authorPhillips, Roger M.
dc.contributor.authorLord, Rianne M.
dc.contributor.authorMcGowan, P.C.
dc.date.accessioned2019-10-02T15:09:49Z
dc.date.available2019-10-02T15:09:49Z
dc.date.issued01/12/2019
dc.identifier.citationMadzivire CR, Carames-Mendez P, Pask CM et al (2019) Anticancer, antifungal and antibacterial potential of bis(β-ketoiminato)ruthenium(II) carbonyl complexes. Inorganica Chimica Acta. 498: 119025.
dc.identifier.urihttp://hdl.handle.net/10454/17284
dc.descriptionNo
dc.description.abstractHerein we report a library of new ruthenium(II) complexes which incorporate a range of functionalised β -ketoiminate ligands. The complexes undergo an unusual reduction from Ru(III) to Ru(II), and consequently incorporate carbonyl ligands from the 2-ethoxyethanol solvent, forming ruthenium dicarbonyl complexes. In order to address the potential applications of these complexes, we have screened the library against a range of tumour cell lines, however, all compounds exhibit low cellular activity and this is tentatively assigned to the decomposition of the compounds in aqueous media. Studies to establish the antifungal and antibacterial potential of these complexes was addressed and show increased growth inhibitions for C. neoformans and S. aureus species.
dc.description.sponsorshipThe authors would like to thank the universities of Leeds, Huddersfield and Bradford for internal financial support.
dc.language.isoen
dc.subjectAnticancer
dc.subjectAntifungal
dc.subjectAntibacteria
dc.subjectRuthenium
dc.subjectBioinorganic chemistry
dc.titleAnticancer, antifungal and antibacterial potential of bis(β-ketoiminato)ruthenium(II) carbonyl complexes
dc.status.refereedYes
dc.date.Accepted17/07/2019
dc.date.application09/08/2019
dc.typeArticle
dc.type.versionNo full-text in the repository
dc.identifier.doihttps://doi.org/10.1016/j.ica.2019.119025
refterms.dateFOA2019-10-02T15:11:59Z
dc.openaccess.statusclosedAccess


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