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- W2740916197 abstract "Dinuclear metal complexes have emerged as a promising class of anticancer compounds with the ability to cross-link biomolecular targets. Here, we describe two novel series of phosphine-linked dinuclear ruthenium(II) p-cymene and gold(I) complexes, in which the length of the connecting poly(ethylene glycol) chain has been systematically modified. The impact of the multinuclearity, lipophilicity, and linker length on the antiproliferative activity of the compounds on tumorigenic (A2780 and A2780cisR) and nontumorigenic (HEK-293) cell lines was assessed. The dinuclear ruthenium(II) complexes were considerably more cytotoxic than their mononuclear counterparts, and a correlation between the lipophilicity of the linker and the cytotoxicity was observed, whereas the cytotoxicity of the gold(I) series is independent of these factors." @default.
- W2740916197 created "2017-08-08" @default.
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- W2740916197 creator A5076539876 @default.
- W2740916197 creator A5078302790 @default.
- W2740916197 date "2017-07-31" @default.
- W2740916197 modified "2023-10-16" @default.
- W2740916197 title "Influence of the Linker Length on the Cytotoxicity of Homobinuclear Ruthenium(II) and Gold(I) Complexes" @default.
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- W2740916197 doi "https://doi.org/10.1021/acs.inorgchem.7b01082" @default.
- W2740916197 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28758743" @default.
- W2740916197 hasPublicationYear "2017" @default.
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