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作 者:杨巧利[1] 郭菁菁[1,2] 代斌玲 俞杭苏 钱朝东[1]
机构地区:[1]浙江中医药大学,杭州310053 [2]绍兴市中心医院
出 处:《中国药师》2016年第8期1442-1445,共4页China Pharmacist
基 金:浙江中医药大学大学生创新创业训练计划项目(编号:781110V005)
摘 要:目的:研究对神经氨酸酶具有抑制作用的槲寄生内生菌次生代谢产物。方法:采用AB-8大孔吸附树脂、C_(18)-SPE柱层析结合制备型HPLC等手段进行分离纯化,根据GC-MS和HPLC等分析手段确定化合物结构,并且利用神经氨酸酶抑制药筛选试剂盒测定活性。结果:从槲寄生内生菌IA-4-2中获得对神经氨酸酶具有较强抑制作用的化合物,经结构鉴定为吲哚-3-甲醛,其对神经氨酸酶的IC50为128.2μg獉ml^(-1)。结论:槲寄生内生菌次生代谢产物吲哚-3-甲醛对神经氨酸酶抑制作用明显,值得进一步研究。Objective: To study the secondary metabolite of mistletoe endophyte with neuraminidase inhibition. Methods: The secondary metabolite of mistletoe endophyte was isolated and purified by AB-8 macroporous absorption resin,C_(18)-SPE column chromatography and preparative HPLC. The structure was elucidated on the basis of GC-MS and HPLC analysis,and the inhibitory activity against neuraminidase was determined by neuraminidase inhibitor screening kit. Results: One secondary metabolite with the inhibitory activity against neuraminidase was found in the culture of mistletoe endophyte IA-4-2,and its structure was determined as indole-3-carboxaldehyde. The IC50 for neuraminidase was 128. 2 μg · ml^(-1). Conclusion: Indole-3-carboxaldehyde produced by mistletoe endophyte shows potential inhibitory activity against neuraminidase,which is worthy of further study.
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