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New half sandwich Ru(II) coordination compounds for anticancer activity
Authors:Bratsos Ioannis  Mitri Elisa  Ravalico Francesco  Zangrando Ennio  Gianferrara Teresa  Bergamo Alberta  Alessio Enzo
Institution:Department of Chemical and Pharmaceutical Sciences, Via L. Giorgieri 1, 34127 Trieste, Italy.
Abstract:With the aim of expanding the structure-activity relationship investigation, the series of Ru(II) half sandwich coordination compounds of the type Ru(9]aneS3)(chel)(L)](n+) previously described by us (where 9]aneS3 is the neutral face-capping ligand 1,4,7-trithiacyclononane, chel is a neutral or anonic chelating ligand, L = Cl(-) or dmso-S, n = 0-2) was extended to 1,4,7-triazacyclononane (9]aneN3). In addition, new neutral N-N, and anionic N-O and O-O chelating ligands, i.e. dach (trans-1,2-diaminocyclohexane), pic(-) (picolinate), and acac(-) (acetylacetonate), were investigated in combination with both 9]aneS3 and 9]aneN3. Overall, ten new half-sandwich complexes were prepared and fully characterized and their chemical behaviour in aqueous solution was established. The single-crystal X-ray structures of eight of them, including the versatile precursor Ru(9]aneN3)(dmso-S)(2)Cl]Cl (9), were also determined. The results of in vitro antiproliferative tests performed on selected compounds against MDA-MB-231 human mammary carcinoma cells confirmed that, in this series, only compounds that hydrolyse the monodentate ligand at a reasonable rate show moderate activity, provided that the chelate ligand is a hydrogen bond donor.
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