伍荣香, 郭杰兰, 黄桦, 廖婧婧, 郝祎, 孔凡栋, 周丽曼, 张朝军. 溶洞真菌Metarhizium anisopliae NHC-M3-2中两个新的异香豆素类化合物J. 药学学报, 2024, 59(9): 2588-2593. DOI: 10.16438/j.0513-4870.2024-0211
引用本文: 伍荣香, 郭杰兰, 黄桦, 廖婧婧, 郝祎, 孔凡栋, 周丽曼, 张朝军. 溶洞真菌Metarhizium anisopliae NHC-M3-2中两个新的异香豆素类化合物J. 药学学报, 2024, 59(9): 2588-2593. DOI: 10.16438/j.0513-4870.2024-0211
WU Rong-xiang, GUO Jie-lan, HUANG Hua, LIAO Jing-jing, HAO Yi, KONG Fan-dong, ZHOU Li-man, ZHANG Chao-jun. Two new isocoumarins from cave-derived Metarhizium anisopliae NHC-M3-2J. Acta Pharmaceutica Sinica, 2024, 59(9): 2588-2593. DOI: 10.16438/j.0513-4870.2024-0211
Citation: WU Rong-xiang, GUO Jie-lan, HUANG Hua, LIAO Jing-jing, HAO Yi, KONG Fan-dong, ZHOU Li-man, ZHANG Chao-jun. Two new isocoumarins from cave-derived Metarhizium anisopliae NHC-M3-2J. Acta Pharmaceutica Sinica, 2024, 59(9): 2588-2593. DOI: 10.16438/j.0513-4870.2024-0211

溶洞真菌Metarhizium anisopliae NHC-M3-2中两个新的异香豆素类化合物

Two new isocoumarins from cave-derived Metarhizium anisopliae NHC-M3-2

  • 摘要: 对来自广西伊岭岩风景区喀斯特溶洞真菌Metarhizium anisopliae NHC-M3-2的次级代谢产物进行提取研究。利用薄层色谱、高效液相色谱等对真菌次级代谢产物进行分离纯化, 得到10个化合物, 其中7-羟基-3-羟甲基-5,6-二甲基异铬-1-酮(1) 与7-羟基-3,5,6-三甲基异铬-1-酮(2) 为新结构的异香豆素类化合物, N-乙酰苯丙氨酸(3)、毛壳素J (4)、2-one-13-hydroxy-3,5,8,7(11)-eudesmatetraen-12,8-olide (5)、1H-吲哚-3-甲醛(6)、irpexolaceus B (7)、irlactin L (8)、细胞松弛素K (9)、烟曲霉酸(10), 共8个已知化合物。运用核磁共振谱、质谱等方法确定化合物结构, 分别采用CCK-8法对化合物进行肿瘤细胞毒活性评价, 结果显示, 新化合物2对HepG2细胞的IC50为29.83 µmol·L-1, 化合物9对HCT116细胞的IC50为27.44 µmol·L-1

     

    Abstract: Extracting extracts of secondary metabolites from the karst cave fungus Metarhizium anisopliae NHC-M3-2 from the Yilingyan Scenic Area in Guangxi. Ten compounds were isolated and purified from fungal secondary metabolites using thin-layer chromatography and high-performance liquid chromatography. 7-Hydroxy-3-hydroxypropyl-5,6-dimethylisochrome-1-one (1) and 7-hydroxy-3,5,6-trimethyl-isochromen-1-one (2) were new isocoumarin compounds, N-acetyl phenylalanine (3), chaetosumin J (4), 2-one-13-hydroxy-3,5,8,7(11)-eudesmatetraen-12,8-olide (5), 1H-indole-3-carboxaldehyde (6), irpexolaceus B (7), irlactin L (8), cytochalasin K (9), and helvolic acid (10), a total of 8 known compounds. The structure of the compound was determined using methods such as NMR and mass spectrometry. The tumor cytotoxicity of the compound was evaluated using the CCK-8 method. The results showed that the IC50 of compound 2 on HepG2 cells was 29.83 µmol·L-1, and compound 9 on HCT116 cells was 27.44 µmol·L-1.

     

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