首页> 美国卫生研究院文献>Molecules >Preparative Isolation and Purification of Three Sesquiterpenoid Lactones from Eupatorium lindleyanum DC. by High-Speed Counter-Current Chromatography
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Preparative Isolation and Purification of Three Sesquiterpenoid Lactones from Eupatorium lindleyanum DC. by High-Speed Counter-Current Chromatography

机译:紫茎泽兰DC中三种倍半萜内酯的制备分离与纯化。通过高速逆流色谱

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摘要

A high-speed counter-current chromatography (HSCCC) method was established for the preparative separation of three sesquiterpenoid lactones from Eupatorium lindleyanum DC. The two-phase solvent system composed of n-hexane–ethyl acetate–methanol–water (1:4:2:3, v/v/v/v) was selected. From 540 mg of the n-butanol fraction of Eupatorium lindleyanum DC., 10.8 mg of 3β-hydroxy-8β-[4'-hydroxy-tigloyloxy]-costunolide, 17.9 mg of eupalinolide A and 19.3 mg of eupalinolide B were obtained in a one-step HSCCC separation, with purities of 91.8%, 97.9% and 97.1%, respectively, as determined by HPLC. Their structures were further identified by ESI-MS and 1H-NMR.
机译:建立了一种高速逆流色谱(HSCCC)方法,用于从刺槐(Eupatorium lindleyanum DC)分离制备三种倍半萜内酯。选择了由正己烷-乙酸乙酯-甲醇-水(1:4:2:3,v / v / v / v)组成的两相溶剂系统。从540mg的莲up中的正丁醇级分中,在a中得到10.8mg的3β-羟基-8β-[4'-羟基-丁氧基酰氧基]-木香内酯,17.9mg的紫杉醇A和19.3mg的紫杉醇B。一步法HSCCC分离,通过HPLC测定,纯度分别为91.8%,97.9%和97.1%。通过ESI-MS和 1 H-NMR进一步鉴定了它们的结构。

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