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Cytotoxic isoferulic acidamide from Myricaria germanica (Tamaricaceae)

机译:来自德国杨​​梅(Tamricaceae)的细胞毒性异阿魏酸酰胺

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摘要

Tamgermanitin, a unique N-trans-Isoferuloyltyramine, together with the hitherto unknown polyphenolics, 2,4-di-O-galloyl-(α/β)-glucopyranose and kaempferide 3,7-disulphate have been isolated from the leaf aqueous ethanol extract of the false tamarisk, Myricaria germanica DESV. In addition, 18 known phenolics were also separated and characterized. All structures were elucidated on the basis of detailed analysis of 1D- 1H and 13C NMR, COSY, HSQC, HMBC and HRFTESIMS spectral data. The extract, its chromatographic column fractions and the isolated isoferuloyltyramine, tamgermanetin demonstrated potential cytotoxic effect against three different tumor cell lines, namely liver (Huh-7), breast (MCF-7) and prostate (PC-3). The IC50''s were found to be substantially low with low-resistance possibility. DNA flow-cytometic analysis indicated that column fractions and tamgermanetin enhanced pre-G apoptotic fraction. Both materials showed inhibiting activity against PARP enzyme activity. In conclusion, we report the isolation and identification of a novel compound, tamgermanitin, from the aqueous ethanol extract of Myricaria germanica leaves. Further, different fractions of the extract and tamgermanitin exhibit potent cytotoxic activities which warrant further investigations.
机译:从叶片乙醇水溶液中分离出Tamgermanitin,一种独特的N-反-异铁氟乙胺,以及迄今未知的多酚,2,4-二-O-galloyl-(α/β)-吡喃葡萄糖和Kaempferide 3,7-二硫酸盐假柳,德国的Myricaria DESV。此外,还分离并表征了18种已知酚类。在详细分析1D- 1 H和 13 C NMR,COSY,HSQC,HMBC和HRFTESIMS光谱数据的基础上阐明了所有结构。提取物,其色谱柱馏分和分离的异铁氟乙胺,坦格曼尼汀对三种不同的肿瘤细胞系,即肝(Huh-7),乳腺(MCF-7)和前列腺(PC-3),均显示出潜在的细胞毒性作用。发现IC50极低,并且具有低电阻的可能性。 DNA流式细胞仪分析表明,柱级分和坦马尼汀增强了前G的凋亡级分。两种材料均显示出对PARP酶活性的抑制活性。总之,我们报告了从德国杨梅叶的乙醇水溶液中分离和鉴定了一种新型化合物坦格曼尼汀。此外,提取物和坦格曼尼汀的不同部分均表现出有效的细胞毒性活性,值得进一步研究。

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