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Platinum(0)-η2-1,2-(E)ditosylethene Complexes Bearing Phosphine, Isocyanide and N-Heterocyclic Carbene Ligands: Synthesis and Cytotoxicity towards Ovarian and Breast Cancer Cells
被引:2
|作者:
Compagno, Nicola
[1
]
Piccolo, Rachele
[1
]
Bortolamiol, Enrica
[1
]
Demitri, Nicola
[2
]
Rizzolio, Flavio
[1
,3
]
Visentin, Fabiano
[1
]
Scattolin, Thomas
[4
]
机构:
[1] Univ Ca Foscari, Dept Mol Sci Nanosyst, Campus Sci,Via Torino 155, I-30174 Venice, Italy
[2] Area Sci Pk Elettra Sincrotrone Trieste, SS 14 Km 163-5, I-34149 Basovizza, Trieste, Italy
[3] Ctr Riferimento Oncol Aviano CRO, Dept Mol Biol & Translat Res, Pathol Unit, IRCCS, Via Franco Gallini 2, I-33081 Aviano, Italy
[4] Univ Padua, Dipartimento Sci Chim, Via Marzolo 1, I-35131 Padua, Italy
来源:
关键词:
platinum(0) complexes;
alkene ligands;
phosphine and isocyanide ligands;
metallodrugs;
N-heterocyclic carbenes;
ovarian and breast cancer;
PLATINUM COMPLEXES;
CISPLATIN;
D O I:
10.3390/molecules29051119
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
A wide range of platinum(0)-eta 2-(E)-1,2-ditosylethene complexes bearing isocyanide, phosphine and N-heterocyclic carbene ancillary ligands have been prepared with high yields and selectivity. All the novel products underwent thorough characterization using spectroscopic techniques, including NMR and FT-IR analyses. Additionally, for some compounds, the solid-state structures were elucidated through X-ray diffractometry. The synthesized complexes were successively evaluated for their potential as anticancer agents against two ovarian cancer cell lines (A2780 and A2780cis) and one breast cancer cell line (MDA-MB-231). The majority of the compounds displayed promising cytotoxicity within the micromolar range against A2780 and MDA-MB-231 cells, with IC50 values comparable to or even surpassing those of cisplatin. However, only a subset of compounds was cytotoxic against cisplatin-resistant cancer cells (A2780cis). Furthermore, the assessment of antiproliferative activity on MRC-5 normal cells revealed certain compounds to exhibit in vitro selectivity. Notably, complexes 3d, 6a and 6b showed low cytotoxicity towards normal cells (IC50 > 100 mu M) while concurrently displaying potent cytotoxicity against cancer cells.
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页数:18
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