CAS Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica , South China Sea Institute of Oceanology, Chinese Academy of Sciences , Guangzhou 510301 , People's Republic of China.
University of Chinese Academy of Sciences , Beijing 100049 , People's Republic of China.
J Nat Prod. 2018 Dec 28;81(12):2722-2730. doi: 10.1021/acs.jnatprod.8b00656. Epub 2018 Dec 5.
A new spirocyclic γ-lactam, named spirostaphylotrichin X (1), and three related known spirostaphylotrichins (2-4) were isolated from the marine-derived fungus Cochliobolus lunatus SCSIO41401. Their structures were determined by spectroscopic analyses. Spirostaphylotrichin X (1) displayed obvious inhibitory activities against multiple influenza virus strains, with IC values from 1.2 to 5.5 μM. Investigation of the mechanism showed that 1 inhibited viral polymerase activity and interfered with the production of progeny viral RNA. Homogeneous time-resolved fluorescence, surface plasmon resonance assays, and a molecular docking study revealed that 1 could inhibit polymerase PB2 protein activity by binding to the highly conserved region of the cap-binding domain of PB2. These results suggest that 1 inhibits the replication of influenza A virus by interfering with the activity of PB2 protein and that 1 represents a new type of potential lead compound for the development of anti-influenza therapeutics.
从海洋来源真菌尖镰孢菌 SCSIO41401 中分离得到一个新的螺环γ-内酰胺,命名为螺环石杉碱 X(1),以及三个相关的已知螺环石杉碱(2-4)。通过光谱分析确定了它们的结构。螺环石杉碱 X(1)对多种流感病毒株表现出明显的抑制活性,IC 值为 1.2-5.5 μM。机制研究表明,1 抑制病毒聚合酶活性并干扰子代病毒 RNA 的产生。均相时间分辨荧光、表面等离子体共振分析和分子对接研究表明,1 可通过与 PB2 蛋白的帽结合结构域的高度保守区域结合来抑制聚合酶 PB2 蛋白的活性。这些结果表明,1 通过干扰 PB2 蛋白的活性来抑制甲型流感病毒的复制,并且 1 代表了一种用于开发抗流感治疗药物的新型潜在先导化合物。