Carrasco Carlos J, Pastor Antonio, Conejo María Del Mar, Álvarez Eleuterio, Calderón-Montaño José Manuel, López-Lázaro Miguel, Galindo Agustín
Departamento de Química Inorgánica, Facultad de Química, Universidad de Sevilla, 41071 Sevilla, Spain.
Instituto de Investigaciones Químicas, CSIC-Universidad de Sevilla, Avda. Américo Vespucio 49, 41092 Sevilla, Spain.
Int J Mol Sci. 2025 Mar 30;26(7):3202. doi: 10.3390/ijms26073202.
Coordination polymers containing zinc and imidazolium-based dicarboxylate ligands, [L], were synthesized by reacting zinc acetate with HL compounds, . The resulting complexes were characterized and structurally identified using single-crystal X-ray diffraction, revealing polymeric structures for the complexes [Zn(L)] (R = Gly, ; βAla, ) and [Zn(L)(HO)] (). In these structures, the [L] ligands adopt a bridging monodentate μ-κ-O,κ-O coordination mode, resulting in distorted tetrahedral (, ) or octahedral () geometries around the zinc center. When the synthesis was carried out in the presence of amino acids, mixed ligand complexes [Zn(L)(aa)(HO)] (R = aa = Val, , and R = aa = Ile, ) were formed. Complexes - were also structurally characterized using single-crystal X-ray crystallography, revealing that the ligand [L] maintained the same coordination mode, while the zinc center adopted a five-coordinated geometry. The cytotoxic activity of complexes - was evaluated against three cancer cell lines and one non-cancerous cell line. Remarkably, these complexes exhibited higher toxicity against cancer cells than against the non-cancerous cell line, and they showed greater selectivity than carboplatin, a commonly used chemotherapy drug. Although, in general, these complexes did not surpass the selectivity of gemcitabine, complex stood out for exhibiting a selectivity index value similar to that of gemcitabine against melanoma cells. Among the series, compounds - demonstrated the highest activity, with being the only complex with some selective activity against lung cancer. Complex was the most active, though with low selectivity, while complex exhibited the highest selectivity for melanoma and bladder cancer (selectivity index of 3.0).
通过使乙酸锌与HL化合物反应,合成了含有锌和咪唑基二羧酸酯配体[L]的配位聚合物。使用单晶X射线衍射对所得配合物进行了表征和结构鉴定,揭示了配合物[Zn(L)](R = Gly, ;βAla, )和[Zn(L)(H₂O)]( )的聚合物结构。在这些结构中,[L]配体采用桥连单齿μ-κ-O,κ-O配位模式,导致锌中心周围出现扭曲的四面体( , )或八面体( )几何构型。当在氨基酸存在下进行合成时,形成了混合配体配合物[Zn(L)(aa)(H₂O)](R = aa = Val, ,以及R = aa = Ile, )。配合物 - 也通过单晶X射线晶体学进行了结构表征,结果表明配体[L]保持相同的配位模式,而锌中心采用五配位几何构型。针对三种癌细胞系和一种非癌细胞系评估了配合物 - 的细胞毒性活性。值得注意的是,这些配合物对癌细胞的毒性高于对非癌细胞系的毒性,并且它们显示出比常用化疗药物卡铂更高的选择性。虽然总体而言,这些配合物没有超过吉西他滨的选择性,但配合物 在对黑色素瘤细胞的选择性指数值方面与吉西他滨相似,表现突出。在该系列中,化合物 - 表现出最高活性, 是唯一对肺癌具有一定选择性活性的配合物。配合物 活性最高,但选择性较低,而配合物 对黑色素瘤和膀胱癌表现出最高选择性(选择性指数为3.0)。