李俊江, 潘银波, 赵江宁, 王荫荫, 张君生, 张华. 南烛内生真菌Cercophora sp. UJN-EF001的次级代谢产物研究J. 药学学报, 2025, 60(12): 3758-3763. DOI: 10.16438/j.0513-4870.2025-1025
引用本文: 李俊江, 潘银波, 赵江宁, 王荫荫, 张君生, 张华. 南烛内生真菌Cercophora sp. UJN-EF001的次级代谢产物研究J. 药学学报, 2025, 60(12): 3758-3763. DOI: 10.16438/j.0513-4870.2025-1025
LI Jun-jiang, PAN Yin-bo, ZHAO Jiang-ning, WANG Yin-yin, ZHANG Jun-sheng, ZHANG Hua. Study on the specialized metabolites from the endophytic fungus Cercophora sp. UJN-EF001 in Vaccinium bracteatumJ. Acta Pharmaceutica Sinica, 2025, 60(12): 3758-3763. DOI: 10.16438/j.0513-4870.2025-1025
Citation: LI Jun-jiang, PAN Yin-bo, ZHAO Jiang-ning, WANG Yin-yin, ZHANG Jun-sheng, ZHANG Hua. Study on the specialized metabolites from the endophytic fungus Cercophora sp. UJN-EF001 in Vaccinium bracteatumJ. Acta Pharmaceutica Sinica, 2025, 60(12): 3758-3763. DOI: 10.16438/j.0513-4870.2025-1025

南烛内生真菌Cercophora sp. UJN-EF001的次级代谢产物研究

Study on the specialized metabolites from the endophytic fungus Cercophora sp. UJN-EF001 in Vaccinium bracteatum

  • 摘要: 利用正相硅胶柱色谱、反相C18柱色谱及高效液相色谱等, 对南烛内生真菌Cercophora sp. UJN-EF001的乙醇浸提物中的小分子化学成分进行分离, 共计得到13个化合物(1~13)。进一步通过高分辨质谱、核磁共振波谱、圆二色谱等谱学方法解析鉴定了这些化合物的结构, 其中包含2个未报道的全新分子(12)、2个首次发现的新天然产物(34)及9个首次从尾孢菌属真菌中分离得到的化合物(5~13)。对这13个化合物进行了α-葡萄糖苷酶抑制活性及一氧化氮(NO)生成抑制活性评价; 结果显示, 这13个化合物对α-葡萄糖苷酶均无明显抑制活性, 而化合物13对脂多糖诱导的RAW264.7巨噬细胞中的NO生成具有较强的抑制活性, IC50值为34.3 ± 3.8 μmol·L-1

     

    Abstract: Thirteen compounds (1-13) were isolated from the ethanol extract of an endophytic fungus Cercophora sp. UJN-EF001 derived from Vaccinium bracteatum, using normal-phase silica gel column chromatography (CC), reversed-phase C18 CC and high-performance liquid chromatography. The structures of these isolates were elucidated through spectroscopic methods including high-resolution mass spectrometry, nuclear magnetic resonance and electronic circular dichroism. Among them, two (1 and 2) were previously unreported molecules, two (3 and 4) were obtained for the first time as natural products, and nine (5-13) were isolated for the first time from the genus Cercophora. All 13 compounds were evaluated for their inhibitory activities against α-glucosidase and nitric oxide (NO) production. As a result, none of them exhibited significant inhibition toward α-glucosidase, while compound 13 displayed moderate inhibition against lipopolysaccharide-induced release of NO in RAW264.7 macrophages with an IC50 value of 34.3 ± 3.8 μmol·L-1.

     

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