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Revelation of antiviral activities by artificial sulfation of a glycosaminoglycan from a marine Pseudomonas

机译:人工硫化来自海洋假单胞菌的糖胺聚糖对抗病毒活性的启示

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摘要

Sulfated derivatives of a glycosaminoglycan containing L-glutamic acid produced by a marine Pseudomonas species, No. 42 strain, were prepared by the method of dicyclohexyl-carbodiimide-mediated reaction. Both low and high degrees of sulfation of the polysaccharides (products A1 and A22, respectively) were investigated for their antiviral activities against influenza virus type A (FluV-A) and B (FluV-B) in MDCK cells. Both preparations showed antiviral acitivity against FluV-A at the 50 percent antiviral effective concentration of 17.3 and 5.2 #mu#g/ml, respectively, whereas they had no antiviral activity against FluV-B. No cytotoxicity of either product was noted against MDCK cells at the 50 percent cytotoxic concentration of 100 #mu#g/ml.
机译:通过二环己基碳二亚胺介导的反应方法,制备了由海洋假单胞菌属42号菌株产生的含有L-谷氨酸的糖胺聚糖的硫酸化衍生物。研究了多糖(分别为产物A1和A22)的低和高硫酸化程度对MDCK细胞中A型流感病毒(FluV-A)和B型流感病毒(FluV-B)的抗病毒活性。两种制剂在50%抗病毒有效浓度分别为17.3和5.2μμg/ ml时均显示出对FluV-A的抗病毒活性,而它们对FluV-B没有抗病毒活性。在100#mu#g / ml的50%细胞毒性浓度下,没有发现任何一种产品对MDCK细胞具有细胞毒性。

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