周丽曼, 郝祎, 蒙菊香, 覃芳芳, 覃清华, 王聪, 孔凡栋. 伊岭岩溶洞真菌Metarhizium anisopliae NHC-M3-2中一个新的萘并吡喃酮糖苷J. 药学学报, 2023, 58(10): 3076-3081. DOI: 10.16438/j.0513-4870.2023-0346
引用本文: 周丽曼, 郝祎, 蒙菊香, 覃芳芳, 覃清华, 王聪, 孔凡栋. 伊岭岩溶洞真菌Metarhizium anisopliae NHC-M3-2中一个新的萘并吡喃酮糖苷J. 药学学报, 2023, 58(10): 3076-3081. DOI: 10.16438/j.0513-4870.2023-0346
ZHOU Li-man, HAO Yi, MENG Ju-xiang, QIN Fang-fang, QIN Qing-hua, WANG Cong, KONG Fan-dong. One new glycoside naphthopyranone from the Yiling cave-derived Metarhizium anisopliae NHC-M3-2J. Acta Pharmaceutica Sinica, 2023, 58(10): 3076-3081. DOI: 10.16438/j.0513-4870.2023-0346
Citation: ZHOU Li-man, HAO Yi, MENG Ju-xiang, QIN Fang-fang, QIN Qing-hua, WANG Cong, KONG Fan-dong. One new glycoside naphthopyranone from the Yiling cave-derived Metarhizium anisopliae NHC-M3-2J. Acta Pharmaceutica Sinica, 2023, 58(10): 3076-3081. DOI: 10.16438/j.0513-4870.2023-0346

伊岭岩溶洞真菌Metarhizium anisopliae NHC-M3-2中一个新的萘并吡喃酮糖苷

One new glycoside naphthopyranone from the Yiling cave-derived Metarhizium anisopliae NHC-M3-2

  • 摘要: 利用硅胶和高效液相等柱色谱方法对溶洞真菌Metarhizium anisopliae NHC-M3-2发酵产物进行分离纯化, 得到了7个化合物。通过紫外、红外、核磁共振谱与质谱方法分别鉴定为2,3-dehydroindigotide G (1)、(-)-regiolone (2)、萘吡喃酮(3)、indigotide G (4)、indigotide B (5)、破伤风毒素A (6) 和破伤风毒素B (7), 其中化合物1为新萘并吡喃酮糖苷类化合物。对分离得到的化合物进行抗乙型肝炎病毒(hepatitis B virus, HBV) 活性测试, 结果显示化合物3的抗HBV作用EC50为4.5 μmol·L-1, CC50为92.3 μmol·L-1, 这是首次报道化合物3的抗病毒活性。

     

    Abstract: Seven compounds were isolated from fermentation extract of cave-derived Metarhizium anisopliae NHC-M3-2 by silica gel, semi-preparative HPLC and other chromatographic methods. Their structures were elucidated by UV, IR, MS and NMR methods as 2,3-dehydroindigotide G (1), (-)-regiolone (2), naphtho-γ-pyrone (3), indigotide G (4), indigotide B (5) destruxin A (6) and destruxin B (7). Compound 1 is a new glycoside naphthopyranone compound. The anti-hepatitis B virus (HBV) activity of these compounds was evaluated. The EC50 and CC50 of compound 3 against HBV were 4.5 μmol·L-1 and 92.3 μmol·L-1, respectively. This is the first report of the antiviral activity of compound 3.

     

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