Synthesis, antimicrobial activity and chemotherapeutic potential of inorganic derivatives of 2-(4′-thiazolyl)benzimidazole thiabendazole:: X-ray crystal structures of [Cu(TBZH)2Cl]C1• H2O•. EtOH and TBZH2NO3 (TBZH = thiabendazole)

被引:84
作者
Devereux, M
McCann, M
Shea, DO
Kelly, R
Egan, D
Deegan, C
Kavanagh, K
McKee, V
Finn, G
机构
[1] Dublin Inst Technol, Dublin 1, Ireland
[2] Natl Univ Ireland Maynooth, Dept Chem, Maynooth, Kildare, Ireland
[3] Dublin Inst Technol, Dept Appl Sci, Dublin 24, Ireland
[4] Natl Univ Ireland Maynooth, Dept Biol, Maynooth, Kildare, Ireland
[5] Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
[6] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Canc Res Programme, Boston, MA 02115 USA
关键词
anti-fungal; Candida; chemotherapeutic potential; metal complexes; thiabendazole;
D O I
10.1016/j.jinorgbio.2004.02.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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. (C) 2004 Elsevier Inc. All rights reserved.
引用
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页码:1023 / 1031
页数:9
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