二氢吡唑衍生物对念珠菌的体外活性研究

Khadija Abdelrahmman , Mohammed F. El-Behairy , Muhammad A. Alsherbiny , Tarek E. Mazeed
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引用次数: 6

摘要

对于由酵母菌(如念珠菌)引起的危险真菌感染的增加,需要对有效的抗真菌药物有深刻的见解。在这项研究中,我们研究了不同的苯二氧唑吡唑啉衍生物对两种念珠菌的功效。所有化合物对两种真菌均表现出有效的体外抗真菌活性。与阳性对照相比,化合物5对白色念珠菌的抑制效果最好。对假丝酵母菌均有活性,阳性对照无活性。这些化合物为开发新的抗菌药物提供了良好的启动模型,特别是对治疗念珠菌病有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro activity of dihydropyrazole derivatives against Candida species

Profound insights for efficient antifungal agents are required for the increased hazardous fungal infections caused by yeast, such as Candida species. In this study, we investigate the efficacy of different benzodioxolpyrazoline derivatives against two Candida species. All compounds exhibited potent in vitro antifungal activity against both species. Compound 5 showed the best inhibition zone in comparison to positive controls for Candida albicans. For Candida parapsilosis, all the tested compounds were active while the positive controls were inactive. These compounds provide good starting models for the development of new antimicrobial agents which could be useful especially for the treatment of candidiasis.

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