Copper(II) coordination compounds with 2-acetylpyridine N4-(bicyclo[2.2.1]heptan-2-yl)thiosemicarbazone as potential antibacterial agents

Vasilii Graur, Ianina Graur, Aurelian Gulea, Iulia Teleuca, Carolina Lozan-Tirsu, Greta Balan
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Abstract

The paper presents the synthesis of the new 2-acetylpyridine N4-(bicyclo[2.2.1]hept-2-yl)thiosemicarbazone (HL) and its three copper(II) coordination compounds: [Cu(L)X] (X = NO3 - (I), Cl- (II), CHCl2COO- (III)). The obtained compounds were studied by NMR and FTIR spectroscopies, elemental analysis, and molar electric conductibility. The antibacterial activity towards Gram-positive (Staphylococcus aureus, Bacillus cereus) and Gram-negative (Escherichia coli, Acinetobacter baumannii) standard strains was studied for the HL and complexes I-III. The coordination of the HL to the copper(II) atom leads to the increase of activity against almost all microorganisms. Complex I is the most active one towards Gram-positive microorganisms, while complex III is the most active one towards Gram-negative microorganisms. They in many cases surpass the activity of Furacillinum and are practically on the same level as Tetracycline towards Gram-positive microorganisms.
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铜(II)配位化合物与2-乙酰吡啶N4-(双环[2.2.1]庚烷-2-基)硫代氨基脲作为潜在的抗菌药物
本文介绍了新型2-乙酰吡啶N4-(双环[2.2.1]庚-2-基)硫代氨基脲(HL)及其铜(II)配位化合物[Cu(L)X] (X = NO3 -(I), Cl- (II), CHCl2COO- (III))的合成。通过核磁共振和红外光谱、元素分析和摩尔电导率对所得化合物进行了研究。研究了其对革兰氏阳性标准菌株(金黄色葡萄球菌、蜡样芽孢杆菌)和革兰氏阴性标准菌株(大肠杆菌、鲍曼不动杆菌)的抑菌活性。HL与铜(II)原子的配位导致对几乎所有微生物的活性增加。配合物I对革兰氏阳性微生物活性最强,而配合物III对革兰氏阴性微生物活性最强。在许多情况下,它们的活性超过了Furacillinum,实际上与四环素对革兰氏阳性微生物的活性处于同一水平。
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