陈晓兰, 杨青青, 陈宣钦, 李蓉涛, 张治军. 连翘中一个新的半日花烷型二萜类化合物J. 药学学报, 2025, 60(3): 755-761. DOI: 10.16438/j.0513-4870.2024-0998
引用本文: 陈晓兰, 杨青青, 陈宣钦, 李蓉涛, 张治军. 连翘中一个新的半日花烷型二萜类化合物J. 药学学报, 2025, 60(3): 755-761. DOI: 10.16438/j.0513-4870.2024-0998
CHEN Xiao-lan, YANG Qing-qing, CHEN Xuan-qin, LI Rong-tao, ZHANG Zhi-jun. A new labdane diterpene compound in Forsythia suspensa (Thunb.) VahlJ. Acta Pharmaceutica Sinica, 2025, 60(3): 755-761. DOI: 10.16438/j.0513-4870.2024-0998
Citation: CHEN Xiao-lan, YANG Qing-qing, CHEN Xuan-qin, LI Rong-tao, ZHANG Zhi-jun. A new labdane diterpene compound in Forsythia suspensa (Thunb.) VahlJ. Acta Pharmaceutica Sinica, 2025, 60(3): 755-761. DOI: 10.16438/j.0513-4870.2024-0998

连翘中一个新的半日花烷型二萜类化合物

A new labdane diterpene compound in Forsythia suspensa (Thunb.) Vahl

  • 摘要: 采用多种色谱分离技术(硅胶柱色谱、MCI柱色谱、Sephadex LH-20凝胶柱色谱等) 对木樨科(Oleaceae) 连翘属植物连翘(Forsythia suspensa) 的果实进行化学成分研究。从其95%乙醇提取部分中分离得到14个萜类化合物, 并通过MS、1D-和2D-NMR等波谱手段和量子化学计算方法进行了结构鉴定: 半日花烷型二萜(1~6)、克罗烷型二萜(7)、降半日花烷型二萜(8)、降克罗烷型二萜(9)、齐墩果烷型三萜(10)、乌苏烷型三萜(11, 12)、羽扇豆烷型三萜(13, 14)。其中化合物1为新化合物, 化合物3~91112为首次从中药连翘中分离得到。评价了这些化合物对脂多糖(LPS) 诱导小鼠巨噬细胞RAW 264.7产生一氧化氮(NO) 的抑制作用, 结果显示这些化合物均未表现出明显的抑制活性。

     

    Abstract: The chemical constituents of the fruits of Forsythia suspensa (Thunb.) Vahl were investigated by using chromatographic techniques (silica gel, MCI, and sephadex LH-20 gel column chromatography, etc). Fourteen compounds were isolated from the 95% ethanol extract of F. suspensa, and their structures were identified by HR-ESI-MS, NMR, and calculated electronic circular dichroism (ECD) methods. The compounds included labdane diterpenes (1-6), clerodane diterpene (7), norlabdane diterpene (8), norclerodane diterpene (9), oleanane triterpenoid (10), ursane triterpenoids (11, 12), lupane triterpenoids (13, 14). Among them, compound 1 was a new compound and compounds 3-9, 11, and 12 were obtained from this plant for the first time. The inhibitory effect of these compounds on lipopolysaccharide-induced nitric oxide production in mouse macrophage RAW 264.7 cells also was evaluated. Unfortunately, none of these compounds exhibited significant inhibitory activity.

     

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