刘云, 胡梦雅, 张文静, 范雨欣, 徐瑞雯, 朱登辉, 孙彦君, 冯卫生, 陈辉. 角茴香中1个新的吡嗪类生物碱J. 药学学报, 2024, 59(1): 183-187. DOI: 10.16438/j.0513-4870.2023-0475
引用本文: 刘云, 胡梦雅, 张文静, 范雨欣, 徐瑞雯, 朱登辉, 孙彦君, 冯卫生, 陈辉. 角茴香中1个新的吡嗪类生物碱J. 药学学报, 2024, 59(1): 183-187. DOI: 10.16438/j.0513-4870.2023-0475
LIU Yun, HU Meng-ya, ZHANG Wen-jing, FAN Yu-xin, XU Rui-wen, ZHU Deng-hui, SUN Yan-jun, FENG Wei-sheng, CHEN Hui. A new pyrazine from Hypecoum erectum L.J. Acta Pharmaceutica Sinica, 2024, 59(1): 183-187. DOI: 10.16438/j.0513-4870.2023-0475
Citation: LIU Yun, HU Meng-ya, ZHANG Wen-jing, FAN Yu-xin, XU Rui-wen, ZHU Deng-hui, SUN Yan-jun, FENG Wei-sheng, CHEN Hui. A new pyrazine from Hypecoum erectum L.J. Acta Pharmaceutica Sinica, 2024, 59(1): 183-187. DOI: 10.16438/j.0513-4870.2023-0475

角茴香中1个新的吡嗪类生物碱

A new pyrazine from Hypecoum erectum L.

  • 摘要: 采用硅胶、ODS、MCI等柱色谱以及半制备液相等现代色谱分离技术对角茴香(Hypecoum erectum L.) 正丁醇萃取部位的化学成分进行分离纯化, 得到4个吡嗪类生物碱。运用现代波谱学方法(1D NMR、2D NMR、UV、IR、MS等) 鉴定结构分别为hyperectpyrazin A (1)、1′S-(6-methylpyrazin-2-yl)-ethane-1′, 2′-diol (2)、2-hydroxymethyl-6-methylpyrazin (3) 和pyrazine-2-carboxylic acid (4)。化合物1为1个新的吡嗪类生物碱, 化合物2~4为首次从角茴香中分离得到, 并首次通过Mo2(OAc)4诱导的CD谱确定了化合物2的绝对构型。采用乙酰胆碱酯酶抑制模型和脂多糖诱导的RAW264.7巨噬细胞炎症模型, 对化合物1~4进行体外活性评价, 其中化合物24表现出一定的乙酰胆碱酯酶抑制活性, 在终浓度为50 μmol·L-1时对乙酰胆碱酯酶的抑制率分别为44.40%和43.99%。

     

    Abstract: Four pyrazines were isolated from the n-butanol fraction of Hypecoum erectum L. by using various chromatographic methods, including MCI gel, ODS, silica gel and semi-preparative HPLC. The structures of the isolated compounds were identified as hyperectpyrazin A (1), 1′S-(6-methylpyrazin-2-yl)-ethane-1′, 2′-diol (2), 2-hydroxymethyl-6-methylpyrazin (3) and pyrazine-2-carboxylic acid (4) by spectroscopy methods (1D NMR, 2D NMR, UV, IR, MS, etc.). The absolute configuration of compound 2 was determined by using the Mo2(OAc)4 induced CD analysis for the first time. Compound 1 was a new compound, compounds 2-4 were isolated from H. erectum for the first time. Compounds 1-4 were evaluated for their inhibition against acetylcholinesterase and nitric oxide generation induced by lipopolysaccharide-RAW264.7 macrophage cells. At a concentration of 50 μmol·L-1, compounds 2 and 4 displayed inhibitory effects on acetylcholinesterase with the inhibition rates of 44.40% and 43.99%, respectively.

     

/

返回文章
返回