Ertan R, Ayhan G, Yulug N, Rolland Y
Ankara University, Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Turkey.
Arzneimittelforschung. 1995 May;45(5):620-3.
In this study some alpha-(1,2,4-triazolyl)acetophenone derivatives were synthesized by the condensation of various triazole and alpha-bromoacetophenone rings. The structures of the compounds have been elucidated by UV, IR, 1H-NMR, mass spectra and elementary analysis. The in vitro antifungal activity of the compounds were investigated against some yeast-like fungi (Candida albicans, C. parapsilosis, C. stellatoidea and C. pseudotropicalis) and moulds such as Trichophyton rubrum and T. mentagrophytes by the tube dilution method and MIC (minimal inhibitory concentration), MFC (minimal fungicidal concentration) values were determined. Compound A16 was significantly more effective than the other compounds. The results obtained for antifungal activity against moulds were not significant.
在本研究中,通过各种三唑环与α-溴苯乙酮环的缩合反应合成了一些α-(1,2,4-三唑基)苯乙酮衍生物。通过紫外光谱、红外光谱、1H-核磁共振光谱、质谱和元素分析对化合物的结构进行了阐明。采用试管稀释法研究了这些化合物对一些酵母样真菌(白色念珠菌、近平滑念珠菌、星状念珠菌和伪热带念珠菌)以及霉菌(如红色毛癣菌和须癣毛癣菌)的体外抗真菌活性,并测定了最低抑菌浓度(MIC)和最低杀菌浓度(MFC)值。化合物A16比其他化合物具有显著更高的活性。所获得的针对霉菌的抗真菌活性结果不显著。