张博文, 李孟, 王小兰, 杨颖, 周诗琪, 陶思琦, 杨梦, 朱登辉, 徐雅桐, 冯卫生, 郑晓珂. 草麻黄根中一个新软木脂类化合物J. 药学学报, 2024, 59(3): 661-666. DOI: 10.16438/j.0513-4870.2023-0729
引用本文: 张博文, 李孟, 王小兰, 杨颖, 周诗琪, 陶思琦, 杨梦, 朱登辉, 徐雅桐, 冯卫生, 郑晓珂. 草麻黄根中一个新软木脂类化合物J. 药学学报, 2024, 59(3): 661-666. DOI: 10.16438/j.0513-4870.2023-0729
ZHANG Bo-wen, LI Meng, WANG Xiao-lan, YANG Ying, ZHOU Shi-qi, TAO Si-qi, YANG Meng, ZHU Deng-hui, XU Ya-tong, FENG Wei-sheng, ZHENG Xiao-ke. A new suberin from roots of Ephedra sinica StapfJ. Acta Pharmaceutica Sinica, 2024, 59(3): 661-666. DOI: 10.16438/j.0513-4870.2023-0729
Citation: ZHANG Bo-wen, LI Meng, WANG Xiao-lan, YANG Ying, ZHOU Shi-qi, TAO Si-qi, YANG Meng, ZHU Deng-hui, XU Ya-tong, FENG Wei-sheng, ZHENG Xiao-ke. A new suberin from roots of Ephedra sinica StapfJ. Acta Pharmaceutica Sinica, 2024, 59(3): 661-666. DOI: 10.16438/j.0513-4870.2023-0729

草麻黄根中一个新软木脂类化合物

A new suberin from roots of Ephedra sinica Stapf

  • 摘要: 采用硅胶柱色谱、薄层色谱和半制备液相等多种色谱学技术从草麻黄根中分离得到6个化合物。根据理化性质与波谱数据鉴定其结构, 分别为(Z)-阿魏酸二十二酯(1)、(E)-阿魏酸二十二酯(2)、邻苯二甲酸-双(2′-乙基庚基)酯(3)、2, 2′-氧代双(1, 4-二叔丁苯) (4)、邻苯二甲酸二异丁酯(5)、邻苯二甲酸二(2-乙基己基)酯(6)。其中化合物1为新化合物, 化合物2~4是首次从麻黄植物中分离得到。采用皮质酮诱导大鼠肾上腺嗜铬细胞瘤(PC-12细胞) 细胞损伤模型进行化合物活性筛选, 结果表明, 化合物15能显著改善皮质酮诱导的PC-12细胞损伤, 并且显著升高细胞中5-HT7 (5-hydroxytryptamine 7) 受体蛋白的表达, 具有潜在的抗抑郁活性。

     

    Abstract: Six compounds were isolated from the roots of Ephedra sinica Stapf using various chromatographic techniques such as silica gel column chromatography, thin layer chromatography and semi-preparative HPLC. Their chemical structures were identified by analysis of physicochemical properties and spectral data, and determined as (Z)-docosanylferulate (1), (E)-docosanylferulate (2), bis (2-ethylheptyl) phythalate (3), 2, 2′-oxybis (1, 4-di-tert-butylbenzene) (4), diisobutyl phthalate (5), bis (2-ethylhexyl) phthalate (6). Among them, compound 1 is a new compound, compounds 2-4 were first isolated from Ephedra. A corticosterone-induced PC-12 cell injury model was used for compound activity screening. The results showed that compounds 1 and 5 significantly improved corticosterone-induced PC-12 cell injury and significantly increased 5-HT7 receptor protein expression in the cells, indicating potential antidepressant activity.

     

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