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New butenolide derivatives from the marine-derived fungus Paecilomyces variotii with DPPH radical scavenging activity

机译:来自海洋真菌的拟青霉新的丁烯内酯衍生物具有DPPH自由基清除活性

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摘要

Bioassay-guided fractionation of the marine-derived endophytic fungus Paecilomyces variotii resulted in the isolation of two new butenolides, namely, butyrolactone IX (1) and aspulvinone O (7), together with eight known related congeners, butyrolactones I, IV, V, and VI (2-5), aspernolide A (6), and aspulvinones H, C, and D (8-10). Their structures were elucidated on the basis of detailed spectroscopic analysis and by comparison with literature data. All of the isolated butenolides were tested for their activity against DPPH radicals and the results showed that butyrolactones (1-6) possessed potent activity with IC50 values ranging from 38.0 to 186.3 mu M, while aspulvinones (7-10) exhibited significant activities with IC50 values ranging from 11.6 to 29.4 mu M, which are stronger than that of the positive control BHT (with IC50 117.7 mu M). The preliminary structure-activity relationship was discussed. (C) 2014 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved.
机译:生物测定指导下的海洋来源内生真菌分枝拟青霉导致分离出两个新的丁烯内酯,即丁内酯IX(1)和阿斯普尔维酮O(7),以及八个已知的相关同源物,丁内酯I,IV,V,和VI(2-5),曲霉内酯A(6)和Aspulvinones H,C和D(8-10)。通过详细的光谱分析并与文献数据进行比较,阐明了它们的结构。测试了所有分离出的丁烯内酯对DPPH自由基的活性,结果表明丁内酯(1-6)具有有效的活性,IC50值为38.0至186.3μM,而阿斯普尔维酮(7-10)则具有显着的IC50活性。值范围从11.6至29.4μM,比阳性对照BHT(IC50为117.7μM)强。初步的构效关系进行了讨论。 (C)2014欧洲植物化学学会。由Elsevier B.V.发布。保留所有权利。

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