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采用高速逆流色谱法从中药蟾酥中制备分离蟾蜍内酯。

Preparative separation and purification of bufadienolides from Chinese traditional medicine of ChanSu using high-speed counter-current chromatography.

机构信息

School of Pharmacy, Dalian Medical University, Dalian, P. R. China.

出版信息

J Sep Sci. 2010 May;33(9):1325-30. doi: 10.1002/jssc.200900782.

Abstract

A preparative high-speed counter-current chromatography method for isolation and purification of bufadienolides from ChanSu was developed by using a stepwise elution with two-phase solvent system composed of n-hexane/ethyl acetate/methanol/water at the ratios of 4:6:2:4 v/v, 4:6:2.5:4 v/v and 4:6:3.2:4 v/v. A total of 3.8 mg of gamabufotalin (1), 7.2 mg of arenobufagin (2), 3.4 mg of telocinobufagin (3), 5.3 mg of bufotalin (4), 8.5 mg of cinobufotalin (5) and 8 mg of bufalin (6) were obtained in one-step separation from 80 mg of the crude extract with purity of 92.7, 96.7, 87.2, 97.3, 94.9 and 99.4%, respectively. Their chemical structures were identified on the basis of (1)H-NMR and (13)C-NMR technology.

摘要

一种制备性高速逆流色谱法,用于从蟾酥中分离和纯化蟾蜍内酯,采用两相溶剂系统,由正己烷/乙酸乙酯/甲醇/水的比例为 4:6:2:4(v/v)、4:6:2.5:4(v/v)和 4:6:3.2:4(v/v)逐步洗脱。从 80mg 粗提取物中一步分离得到 3.8mg 华蟾毒它灵(1)、7.2mg 华蟾酥毒基(2)、3.4mg 远华蟾毒它灵(3)、5.3mg 蟾毒它灵(4)、8.5mg 辛蟾毒精(5)和 8mg 华蟾毒(6),纯度分别为 92.7%、96.7%、87.2%、97.3%、94.9%和 99.4%。根据(1)H-NMR 和(13)C-NMR 技术确定了它们的化学结构。

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