首页|钩吻氧化单萜吲哚生物碱及其抗真菌活性研究

钩吻氧化单萜吲哚生物碱及其抗真菌活性研究

Study on Oxidized Monoterpene Indole Alkaloids and Their Antifungal Activity in Gelsemium Elegans

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目的 著名毒性中药钩吻(Gelsemium elegans)富含单萜吲哚类生物碱(MIAs),前期钩吻的中药化学研究大部分集中于其根茎部位,现对钩吻地上部分生物碱类成分进行研究.方法 采用硅胶柱色谱、MCI柱色谱、高效液相色谱(HPLC)等多种分离技术对于钩吻地上部位总生物碱进行了分离纯化,结合核磁共振波谱(NMR)以及质谱(MS)等结构鉴定手段进行研究.结果 确定了所得单体成分结构,共分离得到5个钩吻定碱类氧化单萜吲哚生物碱,分别鉴定为 19-xo-gelsenicine(1),14-hydroxy-19-oxogelsenicine(2),gelsedilam(3),Nb-methylgelsedilam(4)和gelsemoxonine(5),并对钩吻总生物碱提取物以及化合物1和3的抗真菌的活性进行了评价.结论 经研究发现在100 μg/mL的浓度下钩吻总生物碱提取物对辣椒疫霉菌(Phytophthora capsici)菌丝生长抑制率为34.80%.
Objective:The famous toxic traditional Chinese medicine,Gelsemium elegans,is rich in monoter-pene indole alkaloids(MIAs).Most of the TCM chemical studies on Gelsemium elegans have focused on its root and stem,and now the alkaloids are studied.Methods:The total alkaloids on the ground of Gelsemium elegans were isola-ted and purified by silica gel column chromatography,MCI column chromatography,high performance liquid chroma-tography(HPLC)and other separation techniques,and the structure identification methods such as nuclear magnetic resonance spectroscopy(NMR)and mass spectrometry(MS)were used to conduct the study.Results:The composi-tion and structure of the obtained monomer were determined.Five oxymonoterpene indole alkaloids were isolated and i-dentified as 19-xo-gelsenicine(1),14-hydroxy-19-oxogelsenicine(2),gelsedilam(3),Nb-methylgelsedil-am(4)and gelsemoxonine(5),respectively,and the antifungal activity of the total alkaloid extract and compounds 1 and 3 of Gelsemium elegans were evaluated.Conclusion:The finding shows the total alkaloid extract of Gelsemium ele-gans can inhibit the mycelial growth of phytophthora capsici by 34.80%at the concentration of 100 μg/mL.

Gelsemium ElegansOxidized IndoleAlkaloidsChemical CompositionAntifungal Activity

梁嘉俊、蒲翔、赫卫、潘倩、周永强、周英、魏鑫

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贵州中医药大学,贵州贵阳 550025

钩吻 氧化吲哚 生物碱 化学成分 抗真菌活性

国家自然科学基金贵州中医药大学大学生创新创业训练计划项目

32000276贵中医大创合字[2021]5号

2022

云南中医中药杂志
云南省中医中药研究院,云南省中医药学会

云南中医中药杂志

影响因子:0.598
ISSN:1007-2349
年,卷(期):2022.43(11)
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