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Tethered N-Heterocyclic Carbene-Carboranyl Silver Complexes for Cancer Therapy

机译:用于癌症疗法的束缚正杂环碳甲醛银络合物

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Silver complexes of tethered N-heterocyclic carbene-carboranyl ligands have been prepared and fully characterized. The first example of silver bonded directly to the cage of o-carborane has been identified in the solid state. The presence of a carboranyl N substituent on the N-heterocyclic carbene significantly enhances the in vitro cytotoxicity of the silver complex against HCT116 p53(+/+) and HCT116 p53(-/-) colon cancer cells in comparison to a phenyl derivative. Conversely, the presence of a carboranyl on the backbone of a xanthine-derived N-heterocyclic carbene decreases the in vitro cytotoxicity of the silver complex in comparison to its phenyl derivative. Stability studies on the xanthine-derived ligands and complexes show that decomposition via deboronation occurs in hydrous dimethyl sulfoxide, which may attribute to the contrasting in vitro behaviors of the carborane-containing complexes.
机译:已经制备并完全表征着束缚的N-杂环碳甲醛配体的银络合物。 在固态中鉴定了直接与O-碳硼烷笼中的银键合的第一实施例。 与苯基衍生物相比,N-杂环甲苯上的碳硼酰基N取代基的存在显着增强了对HCT116 P53(+ / +)和HCT116P53( - / - )结肠癌细胞的银复合物的体外细胞毒性。 相反,与其苯基衍生物相比,镁衍生的N-杂环基石的骨干上的碳硼酰基的存在降低了银络合物的体外细胞毒性。 稳定性研究黄嘌呤衍生的配体和复合物的稳定性研究表明,通过衰变的分解发生在含水二甲基亚砜中,其可能归因于含碳硼络合物的体外行为的对比。

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