Rodríguez-Argüelles María C, López-Silva Estefania C, Sanmartín Jesús, Pelagatti P, Zani Franca
Departamento de Química Inorgánica, Universidade de Vigo, 36200 Vigo, Spain.
J Inorg Biochem. 2005 Nov;99(11):2231-9. doi: 10.1016/j.jinorgbio.2005.07.018. Epub 2005 Sep 26.
Copper complexes of thiosemicarbazones of imidazole-2-carbaldehyde, pyrrole-2-carbaldehyde and indole-3-carbaldehyde were synthesised and characterised. The antimicrobial properties of the free ligands and their complexes were evaluated against yeasts, moulds and bacteria (Gram-positive and Gram-negative). Some copper chelates exhibited a moderate inhibitory activity, better than that of the corresponding free ligands. In particular, the pyrrole derivative [Cu(HL(2))(2)] proved to be a wide spectrum agent, showing an interesting inhibition of the growth of all Gram-positive bacteria and fungi tested at concentrations of 12-50 microg/mL. In contrast, a selective effect was observed for imidazole and indole chelates against fungi and Gram-positive bacteria, respectively.
合成并表征了咪唑 - 2 - 甲醛、吡咯 - 2 - 甲醛和吲哚 - 3 - 甲醛的硫代氨基脲铜配合物。评估了游离配体及其配合物对酵母、霉菌和细菌(革兰氏阳性菌和革兰氏阴性菌)的抗菌性能。一些铜螯合物表现出中等抑制活性,优于相应的游离配体。特别是,吡咯衍生物[Cu(HL(2))(2)]被证明是一种广谱剂,在浓度为12 - 50μg/mL时,对所有测试的革兰氏阳性菌和真菌的生长均表现出有趣的抑制作用。相比之下,分别观察到咪唑和吲哚螯合物对真菌和革兰氏阳性菌具有选择性作用。