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(8R,13R)-8,12,13,17-四氢穿心莲内酯的合成、晶体结构和葡萄糖苷酶抑制活性

黄利华1,3, 徐海伟2,3, 刘改芝2,3, 戴桂馥3, 刘宏民1,2,3   

    1. 郑州大学化学系,
    2. 药学院,
    3. 新药研究开发中心, 郑州 450052
  • 收稿日期:2006-10-17 修回日期:1900-01-01 出版日期:2007-07-10 发布日期:2007-07-10
  • 通讯作者: 刘宏民

Synthesis, Crystal Structure and Glucosidase Inhibitory Activities of (8R,13R)-8, 12,13,17-Tetrahydroandrographolide

HUANG Li-Hua, XU Hai-Wei, LIU Gai-Zhi, DAI Gui-Fu, LIU Hong-Min*   

  1. New Drug Research & Development Center, Zhengzhou University, Zhengzhou 450052, China
  • Received:2006-10-17 Revised:1900-01-01 Online:2007-07-10 Published:2007-07-10
  • Contact: LIU Hong-Min

摘要:

设计并合成了新的具有旋光活性的二萜类内酯衍生物2, 并通过NMR, IR, HRMS和X射线单晶衍射等技术分析了其结构和绝对构型.

关键词: 立体选择性还原, 8,12,13,17-四氢穿心莲内酯, 晶体结构, 葡萄糖苷酶, 抑制活性

Abstract:

Some glucosidase inhibitors show antitumor metastasis and anti-HIV activities and are also clinically useful for the treatment of diabetes, besides andrographolide derivative have been proven to be potent an α-glucosidase inhibitor. In order to investigate the double effect of glucosidase inhibition activity, a new diterpene lactone derivative 2 was synthesized via reduction of compound 1 which was one of the constitutions of Andrographis Pamicutate (Brum) Nees. The structure of compound 2 was confirmed with X-ray diffraction analysis, NMR, IR, HR-MS and so on. Compound 2 shows a selective α-glucosidase inhibitory activity with inhibition of 49.6% at 100 μmol/L, and the mother 1 has no inhibition activity(100 μmol/L). The results indicate that the double bond can affect the α-glucosidase inhibition activity of andrographolide.

Key words: Stereoselective reduction, 8,12,13,17-Tetrahydroandrographolide, Crystal structure, Glucosidase, Inhibitory activity

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