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Polyketides and Alkaloids from the Marine-Derived Fungus Dichotomomyces cejpii F31-1 and the Antiviral Activity of Scequinadoline A against Dengue Virus

机译:来自海洋衍生的真菌的聚酮和生物碱Dichotomyces Cejpii F31-1和抗病毒病毒的肌喹唑啉A的抗病毒活性

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摘要

In our continuous chemical investigation on the marine-derived fungus Dichotomomyces cejpii F31-1, two new polyketides dichocetides B-C (1, 2), two new alkaloids dichotomocejs E-F (3, 4), and three known fumiquinozalines: scequinadoline A (5), quinadoline A (6), and scequinadoline E (7) were discovered from the culture broth and the mycelium in the culture medium, by the addition of l-tryptophan and l-phenylalanine. Their chemical structures were established by one dimensional (1D), two dimensional (2D) nuclear magnetic resonance (NMR) and high resolution mass spectrometry (HR-MS) data. Among them, scequinadoline A (5) exhibited significant inhibitory activity against dengue virus serotype 2 production by standard plaque assay, equivalent to the positive control andrographlide. Scequinadoline A (5) possesses the potential for further development as a dengue virus inhibitor.
机译:在我们对海洋衍生的真菌的持续化学调查中Cejpii F31-1,两种新的聚酮化酮二分料酯BC(1,2),两种新的生物碱Dichotomocejs EF(3,4)和三种已知的富马喹唑胺:Scequinadoline A(5),通过加入L-色氨酸和L-苯丙氨酸在培养基中从培养液和菌丝体中发现喹唑啉A(6)和Scequinadoline E(7)。它们的化学结构由一维(1D),二维(2D)核磁共振(NMR)和高分辨率质谱(HR-MS)数据建立。其中,ScequinAdoline A(5)表现出对Dengue病毒血清型2的显着抑制活性通过标准斑块测定产生,其等于阳性对照型和图。 Scequinadoline A(5)具有进一步发展作为登革病毒抑制剂的潜力。

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