化学
白色念珠菌
咪唑
抗菌剂
金黄色葡萄球菌
酮康唑
微生物学
白色体
大肠杆菌
立体化学
硝基咪唑
病菌
细菌
抗真菌
生物化学
有机化学
生物
基因
遗传学
作者
Raymond Rowan,Theresa Tallon,A.M. Sheahan,Robert J. Curran,Malachy McCann,Kevin Kavanagh,Michael Devereux,Vickie McKee
出处
期刊:Polyhedron
[Elsevier]
日期:2005-12-28
卷期号:25 (8): 1771-1778
被引量:91
标识
DOI:10.1016/j.poly.2005.11.021
摘要
Simple synthetic routes are given to the Ag(I) complexes, [Ag2(imH)4](salH)2 (imH = imidazole; salH2 = salicylic acid), [Ag(MeNO2imH)2]ClO4 · nH2O (MeNO2imH = 2-methyl-5-nitroimidazole; n = 1, 3), [Ag(NO2im)] (NO2imH = 5-nitroimidazole) and [Ag(apim)]ClO4 (apim = 1-(3-aminopropyl)imidazole). X-ray crystal structures of [Ag2(imH)4](salH)2, [Ag(MeNO2imH)2]ClO4 · H2O and [Ag(apim)]ClO4 were obtained. The new Ag(I) complexes and related known Ag(I) imidazolates were screened for their growth inhibitory effects (in vitro) against the pathogenic bacteria methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli and also the fungal pathogen Candida albicans. [Ag2(imH)4](salH)2, in comparison to the prescription drug silver sulfadiazine, had significantly better anti-bacterial qualities, whilst against the fungus C. albicans it was 47 times more potent than the marketed drug ketoconazole.
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