首页> 外文期刊>Natural medicines =: 生薬学雜誌 >Quantitative analysis of neosalacinol and neokotalanol, another two potent alpha-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography
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Quantitative analysis of neosalacinol and neokotalanol, another two potent alpha-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography

机译:用离子对色谱法通过LC-MS定量分析来自Salacia物种的另外两种有效的α-葡糖苷酶抑制剂新来新霉素和新可他诺尔

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摘要

A quantitative analytical method for the highly polar sulfonium pseudo-sugar constituents neosalacinol (3) and neokotalanol (4), another two potent a-glucosidase inhibitors isolated from Ayurvedic traditional medicine Salacia species, was developed by employing an ion pair reagent upon chromatographic separation. The optimum conditions for separation and detection of these two constituents were achieved on an ODS column (3-mum particle size, 2.1-mm i.d. x 100 mm) with 5 mM undecafiuoro-hexanoic acid-MeOH (99:1, v/v) as the mobile phase and using MS equipped with an electrospray ionization source. More than ten samples of Salacia from different origins were analyzed, and the results indicated that the assay was reproducible and precise and could be readily utilized for evaluation of a-glucosidase inhibitory activity of Salacia species. By combining this assay with the quantitative analytical method previously developed for salacinol (1) and kotalanol (2), a more precise and strict evaluation of a-glucosidase inhibitory activities of extracts from Salacia species (R - 0.959 for maltase and 0.795 for sucrase) was achieved.
机译:通过色谱分离采用离子对试剂,开发了从阿育吠陀传统药物Salacia中分离出的另外两种有效的α-葡糖苷酶抑制剂的高极性sulf假糖成分新香豆素(3)和新香豆素(4)的定量分析方法。分离和检测这两种成分的最佳条件是在ODS色谱柱上(3微米粒径,内径2.1毫米x 100毫米),使用5 mM十一碳六氢己酸-甲醇(99:1,v / v)作为流动相,并使用配备电喷雾电离源的MS。分析了来自不同来源的十多个Salacia样品,结果表明该方法具有可重复性和精确性,可轻松用于评估Salacia物种的α-葡萄糖苷酶抑制活性。通过将该分析方法与先前开发的用于水杨醇(1)和可可醇(2)的定量分析方法相结合,可以更精确,更严格地评估来自Salacia物种的提取物的α-葡萄糖苷酶抑制活性(R-麦芽糖酶为0.959,蔗糖为0.795)已实现。

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