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Preparative Separation of Alkaloids from Picrasma quassioides (D. Don) Benn. by Conventional and pH-Zone-Refining Countercurrent Chromatography

机译:拟南芥(D. Don)Benn的生物碱的制备分离。常规和pH分区精制逆流色谱法

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Two high-speed countercurrent chromatography (HSCCC) modes were compared by separation of major alkaloids from crude extract of Picrasma quassioides. The conventional HSCCC separation was performed with a two-phase solvent system composed of petroleum ether–ethyl acetate–methanol–water (5:5:4.5:5.5, v/v/v/v) with 200 mg loading. pH-Zone-refining CCC was performed with two-phase solvent system composed of petroleum ether–ethyl acetate–n-butanol–water (3:2:7:9, v/v/v/v) where triethylamine (10 mM) was added to the upper organic stationary phase and hydrochloric acid (5 mM) was added to the lower aqueous phase with 2 g loading. From 2 g of crude extract, 87 mg of 5-methoxycanthin-6-one (a), 38 mg of 1-methoxy-β-carboline (b), 134 mg of 1-ethyl-4,8-dimethoxy-β-carboline (c), 74 mg of 1-ethoxycarbonyl-β-carboline (d), 56 mg of 1-vinyl-4,8-dimethoxy-β-carboline (e) and 26 mg of 1-vinyl-4-dimethoxy-β-carboline (f) were obtained with purities of over 97.0%. The results indicated that pH-zone-refining CCC is an excellent separations tool at the multigram level.
机译:比较了两种高速逆流色谱(HSCCC)模式,方法是从拟生Picrasma quassioides的粗提物中分离主要生物碱。常规的HSCCC分离是在两相溶剂系统中进行的,该系统由200毫克负载的石油醚-乙酸乙酯-甲醇-水(5:5:4.5:5.5,v / v / v / v)组成。使用由石油醚-乙酸乙酯-正丁醇-水(3:2:7:9,v / v / v / v)组成的两相溶剂系统进行pH区域精制CCC,其中三乙胺(10 mM)将有机相加入到上部有机固定相中,并将盐酸(5 mM)以2 g的量加入到下部水相中。从2克粗提物中,提取87毫克5-甲氧基Canthin-6-a(a),38毫克1-甲氧基-β-咔啉(b),134毫克1-乙基-4,8-​​二甲氧基-β-卡宾琳(c),74毫克1-乙氧羰基-β-咔啉(d),56毫克1-乙烯基-4,8-​​二甲氧基-β-咔啉(e)和26毫克1-乙烯基-4-二甲氧基-获得纯度超过97.0%的β-咔啉(f)。结果表明,在克数范围内,pH区精制CCC是一种出色的分离工具。

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