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A new radical scavenging anthracene glycoside, asperflavin ribofuranoside, and polyketides from a marine isolate of the fungus microsporum.

机译:从真菌微孢子菌的海洋分离物中获得的一种新的自由基清除型蒽糖苷,曲黄素核呋喃糖苷和聚酮化合物。

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摘要

A new anthracene glycoside, asperflavin ribofuranoside (1), and the previously described polyketides, flavoglaucin (2), isodihydroauroglaucin (3), and citrinin (4) have been isolated from the marine-derived fungus Microsporum sp. The structure and absolute stereochemistry of a new compound (1) was assigned on the basis of physicochemical data. Compounds 1-3 exhibited a significant radical scavenging activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) with IC(50) values of 14.2, 11.3, and 11.5 muM, respectively, which are more potent than the positive control, ascorbic acid (IC(50), 20 muM). Compound 1 also showed a moderate antibacterial activity against the methicillin-resistant and multidrug-resistant Staphylococcus aureus (MRSA and MDRSA) with MIC value of 50 mug/ml.
机译:从海洋来源的真菌Microsporum sp。中分离出了新的蒽糖苷,曲霉黄素核呋喃糖苷(1)和先前描述的聚酮类化合物,黄酮青霉素(2),异双氢金红霉素(3)和柠檬素(4)。根据理化数据确定了新化合物(1)的结构和绝对立体化学。化合物1-3对1,1-二苯基-2-吡啶并肼基(DPPH)表现出显着的自由基清除活性,IC(50)值分别为14.2、11.3和11.5μM,比阳性对照抗坏血酸更有效酸(IC(50),20μM)。化合物1还显示出对耐甲氧西林和耐多药金黄色葡萄球菌(MRSA和MDRSA)的中等抗菌活性,MIC值为50杯/毫升。

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