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Dimeric 14-Benzoquinone Derivatives with Cytotoxic Activities from the Marine-Derived Fungus Penicillium sp. L129

机译:具有海洋毒性真菌青霉菌sp。的细胞毒活性的二聚14-苯醌衍生物。 L129

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摘要

Two new dimeric 1,4-benzoquinone derivatives, peniquinone A (>1) and peniquinone B (>2), a new dibenzofuran penizofuran A (>3), and a new pyrazinoquinazoline derivative quinadoline D (>4), together with 13 known compounds (>5–>17), were isolated from a marine-derived fungus Penicillium sp. L129. Their structures, including absolute configurations, were elucidated by extensive spectroscopic data and electronic circular dichroism calculations. Compound >1 exhibited cytotoxicity against the MCF-7, U87 and PC3 cell lines with IC50 values of 12.39 µM, 9.01 µM and 14.59 µM, respectively, while compound >2 displayed relatively weak cytotoxicity activities against MCF-7, U87 and PC3 cell lines with IC50 values of 25.32 µM, 13.45 µM and 19.93 µM, respectively. Furthermore, compound >2 showed weak quorum sensing inhibitory activity against Chromobacterium violaceum CV026 with an MIC value of 20 μg/well.
机译:两种新的二聚1,4-苯醌衍生物,戊醌A(> 1 )和戊醌B(> 2 ),一种新的二苯并呋喃Penizofuran A(> 3 ),并从海洋中分离出一种新的吡嗪并喹唑啉衍生物喹啉D(> 4 )以及13种已知化合物(> 5 – > 17 )。真菌青霉L129。广泛的光谱数据和电子圆二色性计算阐明了它们的结构,包括绝对构型。化合物> 1 对MCF-7,U87和PC3细胞系具有细胞毒性,IC50值分别为12.39 µM,9.01 µM和14.59 µM,而化合物> 2 显示相对较弱对MCF-7,U87和PC3细胞系的细胞毒性活性,IC50值分别为25.32 µM,13.45 µM和19.93 µM。此外,化合物> 2 显示出对紫细菌CV026的弱群体感应抑制活性,MIC值为20μg/孔。

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