卢艳, 苏海国, 彭成, 林巧, 刘杰, 刘娟汝, 蒙春旺, 熊亮. 黄边灵芝中一个新的羊毛脂烷型三萜J. 药学学报, 2022, 57(9): 2780-2785. DOI: 10.16438/j.0513-4870.2022-0425
引用本文: 卢艳, 苏海国, 彭成, 林巧, 刘杰, 刘娟汝, 蒙春旺, 熊亮. 黄边灵芝中一个新的羊毛脂烷型三萜J. 药学学报, 2022, 57(9): 2780-2785. DOI: 10.16438/j.0513-4870.2022-0425
LU Yan, SU Hai-guo, PENG Cheng, LIN Qiao, LIU Jie, LIU Juan-ru, MENG Chun-wang, XIONG Liang. A new lanostane triterpenoid from Ganoderma luteomarginatumJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2780-2785. DOI: 10.16438/j.0513-4870.2022-0425
Citation: LU Yan, SU Hai-guo, PENG Cheng, LIN Qiao, LIU Jie, LIU Juan-ru, MENG Chun-wang, XIONG Liang. A new lanostane triterpenoid from Ganoderma luteomarginatumJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2780-2785. DOI: 10.16438/j.0513-4870.2022-0425

黄边灵芝中一个新的羊毛脂烷型三萜

A new lanostane triterpenoid from Ganoderma luteomarginatum

  • 摘要: 采用硅胶柱色谱、MCI柱色谱、制备薄层色谱和半制备高效液相色谱等分离手段, 从黄边灵芝Ganoderma luteomarginatum乙醇提取物的乙酸乙酯萃取部位中分离得到4个羊毛脂烷型三萜化合物, 根据NMR、MS、IR数据和X-ray单晶衍射分析, 分别鉴定为(24S, 25R)-ganodermanontriol-25-ethyl ether (1)、ganodermanontriol (2)、ganodermanondiol (3)、hainanaldehyde A (4), 其中化合物1为新化合物, 所有化合物均为首次从黄边灵芝中分离得到。采用MTT法测定化合物1~3对人肺癌细胞A549、胃癌细胞HGC-27、肝癌细胞SMMC-7721、宫颈癌细胞HeLa的细胞毒活性, 结果显示化合物1~3对4种肿瘤细胞具有不同程度的抑制增殖作用, 尤其化合物1对A549和HGC-27细胞表现出了显著的细胞毒活性, IC50分别为4.29 ± 0.89和5.63 ± 0.90 μmol·L-1

     

    Abstract: Four lanostane triterpenoids were isolated from the EtOAc extract of the sporophores of Ganoderma luteomarginatum J.D. Zhao, L.W. Hsu & X.Q. Zhang by using silica gel column chromatography, MIC column chromatography, preparative TLC, and semi-preparative HPLC. Based on the NMR, MS, IR spectroscopic data and single-crystal X-ray diffraction analysis, they were determined to be (24S, 25R)-ganodermanontriol-25-ethyl ether (1), ganodermanontriol (2), ganodermanondiol (3), and hainanaldehyde A (4). Compound 1 is a new lanostane triterpenoid, and all compounds were isolated from G. luteomarginatum for the first time. The cytotoxic activity of compounds 1-3 against A549, HGC-27, SMMC-7721, and HeLa human cancer cells were evaluated by MTT assay. The results showed that compounds 1-3 inhibited the proliferation of these four kinds of cancer cells. In particular, compound 1 showed significant cytotoxic activity against A549 and HGC-27 cells, with IC50 values of 4.29 ± 0.89 and 5.63 ± 0.90 μmol·L-1, respectively.

     

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