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首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Synthesis, antimicrobial activity and chemotherapeutic potential of inorganic derivatives of 2-(4 '-thiazolyl)benzimidazole thiabendazole: X-ray crystal structures of [Cu(TBZH)(2)Cl]C1 center dot H2O center dot. EtOH and TBZH(2)NO(3) (TBZH = thiabend
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Synthesis, antimicrobial activity and chemotherapeutic potential of inorganic derivatives of 2-(4 '-thiazolyl)benzimidazole thiabendazole: X-ray crystal structures of [Cu(TBZH)(2)Cl]C1 center dot H2O center dot. EtOH and TBZH(2)NO(3) (TBZH = thiabend

机译:2-(4'-噻唑基)苯并咪唑噻菌灵的无机衍生物的合成,抗菌活性和化学治疗潜力:[Cu(TBZH)(2)Cl] C1中心点H2O中心点的X射线晶体结构。 EtOH和TBZH(2)NO(3)(TBZH =硫苯end

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Thiabendazole (TBZH) reacts with iron(III) nitrate causing protonation of the ligand to yield the nitrate salt [TBZH(2)NO(3)] (1). Reaction of TBZH with copper(II) acetate results in the deprotonation of the ligand yielding [Cu(TBZ)(2) (.) (H2O)(2)] (2). Reactions of TBZH with the chloride, nitrate and butanedioate salts of copper(II) yields [Cu(TBZH)(2)Cl]Cl (.) H2O (.) EtOH (3), [Cu(TBZH)(2)(NO3)(2)] (4) and [Cu(TBZH)(O2C-CH2CH2-CO2)] (5), respectively. The TBZH acts as a neutral chelating ligand in 3-5. Molecular structures of 1 and 3 were determined crystallographically. In 1, the asymmetric unit contains one TBZH(2)(+) cation and one NO3- anion. 2 The structure of 3 comprises a five coordinate copper centre with the metal bound to two chelating TBZH ligands and one chloride. The geometry is best described as trigonal bipyramidal. Hydrogen bonding connects the complex cation with the uncoordinated chloride anion and the water and ethanol solvate molecules. Compound 1 and the copper complexes 2-5, the metal free ligands and a number of simple copper(II) salts were each tested for their ability to inhibit the growth of Candida albicans. The metal free TBZH and its nitrate salt (1) exhibited very poor activity. Complex 2, in which the TBZH is present as an anionic ligand (TBZ(-)), exhibits moderate activity towards the pathogen. Chelation of the neutral TBZH to copper centres (complexes 3-5) results in potent anti-candida activity. The dimethyl sulphoxide (DMSO) soluble complexes 3 and 4, along with metal free TBZH were assessed for their cancer chemotherapeutic potential towards two human epithelial-derived cancer model cell lines. Complexes 3 and 4 displayed similar dose-dependent cytotoxicity in both cell lines with IC50 values of approximately 50 muM, which were found to be significantly lower than that for metal free TBZH.
机译:噻苯达唑(TBZH)与硝酸铁(III)反应,使配体质子化,生成硝酸盐[TBZH(2)NO(3)](1)。 TBZH与乙酸铜(II)的反应导致配体去质子化,生成[Cu(TBZ)(2)(。)(H2O)(2)](2)。 TBZH与铜(II)的氯化物,硝酸盐和丁二酸盐反应生成[Cu(TBZH)(2)Cl] Cl(。)H2O(。)EtOH(3),[Cu(TBZH)(2)(NO3 )(2)](4)和[Cu(TBZH)(O2C-CH2CH2-CO2)](5)。 TBZH在3-5中充当中性螯合配体。 1和3的分子结构通过晶体学确定。在图1中,不对称单元包含一个TBZH(2)(+)阳离子和一个NO3-阴离子。 2 3的结构包括一个五配位的铜中心,金属与两个螯合的TBZH配体和一个氯化物键合。最好将几何描述为三角双锥体。氢键将配位阳离子与未配位的氯阴离子以及水和乙醇溶剂化物分子连接起来。分别测试了化合物1和铜络合物2-5,无金属的配体和许多简单的铜(II)盐抑制白色念珠菌生长的能力。不含金属的TBZH及其硝酸盐(1)的活性非常差。 TBZH作为阴离子配体(TBZ(-))存在的复合物2对病原体具有中等活性。中性TBZH与铜中心(配合物3-5)的螯合导致有效的抗念珠菌活性。评估了二甲基亚砜(DMSO)可溶性复合物3和4,以及不含金属的TBZH对两种人类上皮来源的癌症模型细胞系的癌症化疗潜力。复合物3和4在两种细胞系中均显示出相似的剂量依赖性细胞毒性,IC50值约为50μM,这被发现显着低于不含金属的TBZH。

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