Chinese folk medicine “Liang Tou Jian”(Anemone raddeana Regel) is the important medicine used to treat rheumatism, neuralgia, cancer and so on. Its chemical constituents were studied by chromatographing on silica ge...Chinese folk medicine “Liang Tou Jian”(Anemone raddeana Regel) is the important medicine used to treat rheumatism, neuralgia, cancer and so on. Its chemical constituents were studied by chromatographing on silica gel and HPLC. A new triterpenoid saponin, raddeanoside 18, along with two known triterpenoid saponins, Hederacholichiside F and Leontoside D, was isolated from the ethanolic extrant of the rhizoma of Anemone raddeana Regel. Their structures were elucidated as 3-O-β-D-glucopyranosyl(1→4)[β-D-glucopyranosyl(1→2)]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside(1), 3-O-β-D-glucopyranosyl(1→4)[α-L-rhamnopyranosyl(1→2)-]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside(2), 3-O-β-D-glucopyranosyl(1→4)-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside(3) by 1D and 2D NMR ESI-MS and IR spectrometries, respectively.展开更多
文摘对土鳖虫水浸醇沉提取物2号样品进行了离子交换柱层析,得组分Ⅰ、Ⅱ、Ⅲ。实验结果表明,组分Ⅲ的溶栓活性明显高于组分Ⅰ和组分Ⅱ,其蛋白质含量为88.9%,分子量约为38,018,效价为313 UK/mg,比活力为352 UK/mg蛋白。将组分Ⅲ再进行凝胶过滤柱层析,得组分Ⅳ、Ⅴ、Ⅵ。组分Ⅵ的生物活性高于组分Ⅳ和组分Ⅴ,蛋白质含量为89.3%,电泳呈现两条带,分子量约为34,623和39,811,效价为77 UK/mg,比活力为86 UK/mg蛋白。将组分Ⅵ进行反相高效液相色谱柱层析,收集保留时间为17 m in的洗脱峰,得到土鳖虫纯蛋白质,呈白色絮状,极易溶于水。再一次用反相高效液相色谱检查其纯度,保留时间为17.073 m in,无杂质峰。纤溶活性实验结果表明,组分Ⅵ既有直接降解纤维蛋白的作用,同时也有纤溶酶原激活剂样作用。
文摘Chinese folk medicine “Liang Tou Jian”(Anemone raddeana Regel) is the important medicine used to treat rheumatism, neuralgia, cancer and so on. Its chemical constituents were studied by chromatographing on silica gel and HPLC. A new triterpenoid saponin, raddeanoside 18, along with two known triterpenoid saponins, Hederacholichiside F and Leontoside D, was isolated from the ethanolic extrant of the rhizoma of Anemone raddeana Regel. Their structures were elucidated as 3-O-β-D-glucopyranosyl(1→4)[β-D-glucopyranosyl(1→2)]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside(1), 3-O-β-D-glucopyranosyl(1→4)[α-L-rhamnopyranosyl(1→2)-]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside(2), 3-O-β-D-glucopyranosyl(1→4)-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl(1→4)-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside(3) by 1D and 2D NMR ESI-MS and IR spectrometries, respectively.
