Antiproliferative Sorbicillinoids From the Deep-Sea-Derived Penicillium allii-sativi.

Antiproliferative Sorbicillinoids From the Deep-Sea-Derived Penicillium allii-sativi.
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来自深度衍生的青霉alii-sativi的抗增生性山间霉素。

DOI:
10.3389/fmicb.2020.636948
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发表时间:
2020
影响因子:
5.2
通讯作者:
Chen HF
Chen HF
中科院分区:
生物学2区
文献类型:
--
作者:
Xie CL;Zhang D;Lin T;He ZH;Yan QX;Cai Q;Zhang XK;Yang XW;Chen HF

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从深海来源的葱青霉菌MCCC 3A00580中分离到2个新的(1-2)和3个已知的(3-5)山梨壳酸。化合物1和2分别命名为山梨糖儿茶酚C和D,是两种新的杂化二氢山梨十亿酸酯。它们的结构主要通过光谱分析和电子圆二色性(ECD)计算确定。5个分离株分别对MCF-7、HT-29、HuH-7和LNCap 4种肿瘤细胞系进行了抗增殖活性测试。化合物2和5对HT-29细胞具有良好的剂量依赖性。机制研究发现,它们可以通过提高p-H3和cyclin B1的蛋白水平显著诱导细胞周期G2-M期阻滞。
Two new (1–2) and three known (3–5) sorbicillinoids were isolated from the deep-sea-derived fungus Penicillium allii-sativi MCCC 3A00580. Compounds 1 and 2, named sorbicatechols C and D, were two new hybrid dihydrosorbillinoids. Their structures were established mainly by spectroscopic analyses and electronic circular dichroism (ECD) calculations. All five isolates were tested for antiproliferative activities against four tumor cell lines of MCF-7, HT-29, HuH-7, and LNCap. Compounds 2 and 5 inhibited HT-29 cells in a good dose-dependent manner. Mechanism investigation uncovered that they could significantly induce cell cycle G2-M phase arresting by increasing the protein levels of p-H3 and cyclin B1.
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