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Hybrid Polyketides from a Hydractinia-Associated Cladosporium sphaerospermum SW67 and Their Putative Biosynthetic Origin

机译:与水合作用的球孢白粉病SW67杂合聚酮化合物及其推测的生物合成来源

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摘要

Five hybrid polyketides ( , , and – ) containing tetramic acid core including a new hybrid polyketide, cladosin L ( ), were isolated from the marine fungus SW67, which was isolated from the marine hydroid polyp of . The hybrid polyketides were isolated as a pair of interconverting geometric isomers. The structure of was determined based on 1D and 2D NMR spectroscopic and HR-ESIMS analyses. Its absolute configuration was established by quantum chemical electronic circular dichroism (ECD) calculations and modified Mosher’s method. Tetramic acid-containing compounds are reported to be derived from a hybrid PKS-NRPS, which was also proved by analyzing our C-labeling data. We investigated whether compounds – could prevent cell damage induced by cisplatin, a platinum-based anticancer drug, in LLC-PK1 cells. Co-treatment with and ameliorated the damage of LLC-PK1 cells induced by 25 μM of cisplatin. In particular, the effect of compound at 100 μM (cell viability, 90.68 ± 0.81%) was similar to the recovered cell viability of 88.23 ± 0.25% with 500 μM -acetylcysteine (NAC), a positive control.
机译:从海洋真菌SW67中分离了5种含有mic酸核心的杂多聚酮(,和-),包括一种新的杂聚酮,cladassin L()。杂化聚酮化合物被分离为一对相互转化的几何异构体。基于1D和2D NMR光谱以及HR-ESIMS分析确定的结构。它的绝对构型是通过量子化学电子圆二色性(ECD)计算和改进的Mosher方法建立的。据报道,含四甲酸的化合物衍生自杂种PKS-NRPS,这也通过分析我们的C标记数据得到了证明。我们研究了化合物是否可以预防LLC-PK1细胞中由铂基抗癌药顺铂诱导的细胞损伤。与25μM顺铂诱导的LLC-PK1细胞共同治疗并改善其损伤。特别地,化合物在100μM(细胞活力,90.68±0.81%)下的作用类似于使用500μM乙酰半胱氨酸(NAC)(阳性对照)的回收细胞活力,在88.23±0.25%的情况下。

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