何晨, 曹彦刚, 齐曼, 张贝贝, 任英杰, 刘晏灵, 王梦娜, 郑晓珂, 冯卫生. 皂角刺中的一个新木脂素J. 药学学报, 2020,55(12): 2951-2954. doi: 10.16438/j.0513-4870.2020-1241
引用本文: 何晨, 曹彦刚, 齐曼, 张贝贝, 任英杰, 刘晏灵, 王梦娜, 郑晓珂, 冯卫生. 皂角刺中的一个新木脂素J. 药学学报, 2020,55(12): 2951-2954. doi: 10.16438/j.0513-4870.2020-1241
HE Chen, CAO Yan-gang, QI Man, ZHANG Bei-bei, REN Ying-jie, LIU Yan-ling, WANG Meng-na, ZHENG Xiao-ke, FENG Wei-sheng. A new lignan from Gleditsiae spinaJ. Acta Pharmaceutica Sinica, 2020,55(12): 2951-2954. doi: 10.16438/j.0513-4870.2020-1241
Citation: HE Chen, CAO Yan-gang, QI Man, ZHANG Bei-bei, REN Ying-jie, LIU Yan-ling, WANG Meng-na, ZHENG Xiao-ke, FENG Wei-sheng. A new lignan from Gleditsiae spinaJ. Acta Pharmaceutica Sinica, 2020,55(12): 2951-2954. doi: 10.16438/j.0513-4870.2020-1241

皂角刺中的一个新木脂素

A new lignan from Gleditsiae spina

  • 摘要: 利用MCI gel CHP-20、ODS、Sephadex LH-20、硅胶及半制备高效液相等多种色谱技术,从皂角刺乙酸乙酯部位分离得到7个木脂素类化合物,并根据波谱数据分析鉴定其结构,分别为(7R,8S,7'E,7''S,8''R)-buddlenol P(1)、(+)-丁香脂素(2)、(+)-异落叶松脂素(3)、(7S,8R)-cedrusin(4)、(7S,8R)-4,9,9'-三羟基-3,3'-二甲氧基-7,8-二氢苯骈呋喃-1'-丙基新木脂素(5)、3',4-O-dimethylcedrusin(6)和蛇菰宁(7)。其中化合物1为新化合物,命名为(7R,8S,7'E,7''S,8''R)-buddlenol P,化合物27为首次从皂荚属中分离得到。采用MTT法探究化合物27对脂多糖(LPS)诱导的大鼠肾小管上皮细胞损伤的干预作用,化合物237对LPS诱导的NRK-52e细胞损伤具有保护作用。

     

    Abstract: The chemical constituents from ethyl acetate extract of Gleditsiae spina were isolated and purified by various chromatographic methods such as MCI gel CHP-20, ODS, Sephadex LH-20, silica gel and semi-preparative HPLC. Seven lignans were isolated and identified by spectroscopic data analyses as (7R,8S,7'E,7''S,8''R)-buddlenol P (1), (+)-syringaresinol (2), (+)-isolariciresinol (3), (7S,8R)-cedrusin (4), (7S,8R)-4,9,9'-trihydroxy-3,3'-dimethoxy-7,8-dihydrobenzofuran-1'-propylneolignan (5), 3',4-O-dimethylcedrusin (6), balanophonin (7). Among them, compound 1 is a new lignan, compounds 2-7 are isolated from the Gleditsia L. for the first time. MTT method was used to investigate the effect of compounds 2-7 on LPS-induced injury of NRK-52e cells. As a result, compounds 2, 3 and 7 exhibit protective effects against LPS-induced damage to NRK-52e cells.

     

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