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海洋来源真菌 F31-1 中的聚酮类化合物和生物碱及 Scequinadoline A 的抗登革病毒活性。

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

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.

School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China.

出版信息

Mar Drugs. 2018 Jul 6;16(7):229. doi: 10.3390/md16070229.

DOI:10.3390/md16070229
PMID:29986460
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6071211/
Abstract

In our continuous chemical investigation on the marine-derived fungus F31-1, two new polyketides dichocetides B-C (, ), two new alkaloids dichotomocejs E-F (, ), and three known fumiquinozalines: scequinadoline A (), quinadoline A (), and scequinadoline E () 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 () exhibited significant inhibitory activity against dengue virus serotype 2 production by standard plaque assay, equivalent to the positive control andrographlide. Scequinadoline A () possesses the potential for further development as a dengue virus inhibitor.

摘要

在对海洋来源真菌 F31-1 的持续化学研究中,从发酵液和发酵培养基中的菌丝体中,通过添加 l-色氨酸和 l-苯丙氨酸,发现了两种新的聚酮类化合物二氢头孢菌素 B-C(1,2)、两种新的生物碱二氢托莫乔辛 E-F(3,4)以及三种已知的夫喹啉嗪类化合物:色喹那丁 A(5)、喹那丁 A(6)和色喹那丁 E(7)。通过一维(1D)、二维(2D)核磁共振(NMR)和高分辨率质谱(HR-MS)数据确定了它们的化学结构。其中,色喹那丁 A(5)在标准蚀斑试验中对登革热病毒血清型 2 的产生表现出显著的抑制活性,与阳性对照化合物穿心莲内酯相当。色喹那丁 A(5)具有作为登革热病毒抑制剂进一步开发的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/6b4dc48fcbde/marinedrugs-16-00229-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/57c73c8e882e/marinedrugs-16-00229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/245579ef52de/marinedrugs-16-00229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/d791fb6ef790/marinedrugs-16-00229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/6b4dc48fcbde/marinedrugs-16-00229-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/57c73c8e882e/marinedrugs-16-00229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/245579ef52de/marinedrugs-16-00229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/d791fb6ef790/marinedrugs-16-00229-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b7/6071211/6b4dc48fcbde/marinedrugs-16-00229-g004.jpg

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