曹彦刚, 郭孟焕, 赵怡欣, 刘晏灵, 陈旭, 郑晓珂, 冯卫生. 零余子中一对新的二苯基庚烷对映体J. 药学学报, 2025, 60(10): 3146-3151. DOI: 10.16438/j.0513-4870.2025-0545
引用本文: 曹彦刚, 郭孟焕, 赵怡欣, 刘晏灵, 陈旭, 郑晓珂, 冯卫生. 零余子中一对新的二苯基庚烷对映体J. 药学学报, 2025, 60(10): 3146-3151. DOI: 10.16438/j.0513-4870.2025-0545
CAO Yan-gang, GUO Meng-huan, ZHAO Yi-xin, LIU Yan-ling, CHEN Xu, ZHENG Xiao-ke, FENG Wei-sheng. A pair of new diarylheptanoid enantiomers from bulbils of Dioscorea opposite Thunb.J. Acta Pharmaceutica Sinica, 2025, 60(10): 3146-3151. DOI: 10.16438/j.0513-4870.2025-0545
Citation: CAO Yan-gang, GUO Meng-huan, ZHAO Yi-xin, LIU Yan-ling, CHEN Xu, ZHENG Xiao-ke, FENG Wei-sheng. A pair of new diarylheptanoid enantiomers from bulbils of Dioscorea opposite Thunb.J. Acta Pharmaceutica Sinica, 2025, 60(10): 3146-3151. DOI: 10.16438/j.0513-4870.2025-0545

零余子中一对新的二苯基庚烷对映体

A pair of new diarylheptanoid enantiomers from bulbils of Dioscorea opposite Thunb.

  • 摘要: 零余子为薯蓣科植物薯蓣Dioscorea opposite Thunb.的叶腋下株芽。本研究采用Diaion HP-20、MCI gel CHP-20、Sephadex LH-20等多种色谱技术结合半制备高效液相分离纯化, 从零余子中分离得到9个化合物, 采用核磁共振谱、质谱等手段鉴定所得化合物的结构, 分别为(±)-diosniponol G (1)、neo-olivil (2)、异落叶松脂素(3)、bombasin (4)、异夏佛塔苷(5)、皂草黄苷(6)、芹菜素-6-C-α-L-阿拉伯糖-7-O-β-D-葡萄糖苷(7)、2-hydroxy-3, 5, 7-trimethoxy-9, 10-dihydrophenanthrene (8)、albibrissinoside B (9)。其中, 化合物1为一对新的二苯基庚烷对映体, 其他化合物均为首次从薯蓣中分离得到。筛选了化合物1~9α-葡萄糖苷酶抑制活性, 发现所有化合物在100 μmol·L-1浓度下均未表现出明显的抑制活性。

     

    Abstract: Nine compounds were isolated and identified as (±)-diosniponol G (1), neo-olivil (2), isolariciresinol (3), bombasin (4), isoschaftoside (5), saponarin (6), apigenin 6-C-α-L-arabinopyranosyl-7-O-β-D-glucopyranoside (7), 2-hydroxy-3, 5, 7-trimethoxy-9, 10-dihydrophenanthrene (8), and albibrissinoside B (9) from bulbils of Dioscorea opposite Thunb. by multiple column chromatographic methods including Diaion HP-20, MCI gel CHP-20, and Sephadex LH-20. Compound 1 was a new pair of diarylheptanoid enantiomers, and the other compounds were isolated from D. opposite for the first time. The α-glucosidase inhibitory activities of the isolates were screened, and no compound exhibited significantly inhibitory activity against α-glucosidase at the concentration of 100 μmol·L-1.

     

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