Antifungal activity of 2α,3β-functionalized steroids stereoselectively increases with the addition of oligosaccharides

被引:5
作者
Cammarata, Amy [1 ]
Upadhyay, Sunil Kumar [2 ]
Jursic, Branko S. [2 ]
Neumann, Donna M. [1 ,3 ,4 ]
机构
[1] LSUHSC, Dept Pharmacol & Expt Therapeut, New Orleans, LA 70112 USA
[2] Univ New Orleans, Dept Chem, New Orleans, LA 70148 USA
[3] LSUHSC Eye Ctr Excellence, New Orleans, LA USA
[4] LSUHSC, Dept Genet, New Orleans, LA 70112 USA
关键词
Spirostanes; Cholestanes; Antifungal; Glycosides; SAPONIN; CAY-1;
D O I
10.1016/j.bmcl.2011.10.015
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Invasive fungal infections pose a significant problem to the immune-compromised. Moreover, increased resistance to common antifungals requires development of novel compounds that can be used to treat invasive fungal infections. Naturally occurring steroidal glycosides have been shown to possess a range of functional antimicrobial properties, but synthetic methodology for their development hinders thorough exploration of this class of molecules and the structural components required for broad spectrum antifungal activity. In this report, we outline a novel approach to the synthesis of glycoside-linked functionalized 2 alpha,3 beta-cholestane and spirostane molecules and present data from in vitro screenings of the antifungal activities against human fungal pathogens and as well as mammalian cell toxicity of these derivatives. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7379 / 7386
页数:8
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