流感病毒夺帽活性新抑制剂卵孢蛋白的发现

Nobuhiro Koyama, Y. Shibagaki, Mitsuru Okuwaki, S. Hattori, H. Tomoda
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引用次数: 0

摘要

在我们筛选微生物来源的过程中,我们发现真菌菌株BF-0073产生一种流感病毒夺帽活性的抑制剂。化合物(1)采用溶剂萃取和制备高效液相色谱法从真菌BF-0073培养液中分离得到。通过质谱和核磁共振分析,鉴定其为卵孢蛋白。化合物1抑制甲型流感病毒的cap- snatchactivity呈剂量依赖性,IC50值为20.0 μg/mL。图1:卵孢蛋白的结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery of Oosporein as a New Inhibitor of Influenza Virus Cap-snatching Activity
During our screening of microbial origins, we found that fungal strain BF-0073 produces an inhibitor of the cap-snatching activity of influenza virus. Compound (1) was isolated from the culture broth of fungal strain BF-0073 by solvent extraction and preparative HPLC. Based on structural analyses using MS and NMR, 1 was identified as oosporein. Compound 1 inhibited the cap-snatching activity of influenza virus A in a dose-dependent manner, with an IC50 value of 20.0 μg/mL. Figure 1: Structure of oosporein.
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