Preparative isolation and purification of four prenylflavanones from microbial biotransformation of kurarinone by high-speed counter-current chromatography

被引:11
|
作者
Ma, Xiao-chi [2 ]
Sun, Changkai [3 ]
Huang, Shan-shan [2 ]
Wang, Jin-kui [2 ]
Zhang, Bao-jing [2 ]
Li, Feng-yun [2 ]
Wang, Gang [2 ]
Deng, Sha [2 ]
Cui, Jian [1 ]
机构
[1] Chinese Minor Tradit Med Ctr, Ctr Univ Nationalities, Beijing 10081, Peoples R China
[2] Dalian Med Univ, Sch Pharm, Dalian 116044, Peoples R China
[3] Dalian Med Univ, Brain Dis Inst Liaoning Prov, Dalian 116044, Peoples R China
关键词
Kurarinone; Biotransformation; Counter-current chromatography; Separation; SOPHORA-FLAVESCENS; STRUCTURAL DETERMINATION; PRENYLATED FLAVONOIDS; TRANSFORMATION; SEPARATION; CURDIONE; ROOTS; PLANT; ACID;
D O I
10.1016/j.seppur.2010.09.033
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A preparative high-speed counter-current chromatography (HSCCC) method for isolation and purification of four prenylflavanones from the crud extract after microbial biotransformation of kurarinone was developed successfully using a stepwise elution with two-phase solvent system composed n-hexane-ethyl acetate-methanol-water at the volume ratios of 1:1:0.7:1 (v/v) and 1:1:1.2:1 (v/v). A total of 7 mg of 4a,5a-dihydroxy norkurarinone (1), 11 mg of 7-methoxyl-4a,5a-dihydroxy norkurarinone (2), 14 mg of 6a-hydroxykurarinone (3) and 10 mg of norkurarinone (4) were obtained in one-step separation from 520 mg of the crude biotransformation sample with purities of 94.0%, 97.8%, 99.5% and 98.7%, respectively. Among them, compounds 1-3 are novel compounds, and their chemical structures were identified on the basis of the extensive spectral methods such as UV, IR, HR-MS and NMR. (C) 2010 Published by Elsevier B.V.
引用
收藏
页码:140 / 145
页数:6
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