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首页> 外文期刊>Fitoterapia >Biotransformation on the flavonolignan constituents of Silybi Fructus by an intestinal bacterial strain Eubacterium limosum ZL-II
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Biotransformation on the flavonolignan constituents of Silybi Fructus by an intestinal bacterial strain Eubacterium limosum ZL-II

机译:肠道细菌E.bacterium limosum ZL-II对水飞蓟黄素木脂素成分的生物转化

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Eubacterium limosum ZL-II is an anaerobic bacterium with demethylated activity, which was isolated from human intestinal bacteria in our previous work. In this study, the flavonolignan constituents of Silybi Fructus were biotransformed by E. limosum(1) ZL-II, producing four new transformation products - demethylisosilybin B (T1), demethylisosilybin A (T2), demethylsilybin B (T3) and demethylsilybin A (T4), among which T1 and T2 were new compounds. Their chemical structures were identified by ESI-TOF/MS, H-1 NMR, C-13 NMR, HMBC and CD spectroscopic data. The bioassay results showed that the transformation products T1-T4 exhibited significant inhibitory activities on Alzheimer's amyloid-beta 42 (A beta(2)(42)) aggregation with IC50 values at 7.49 mu M-10.46 mu M, which were comparable with that of the positive control (epigallocatechin gallate, EGCG(3), at 9.01 mu M) and much lower than those of their parent compounds (at not less than 145.10 mu M). The method of biotransformation by E. limosum ZL-II explored a way to develop the new and active lead compounds in Alzheimer's disease from Silybi Fructus. However, the transformation products T1-T4 exhibited decreased inhibitory activities against human tumor cell lines comparing with their parent compounds
机译:Limoum limosum ZL-II是一种具有去甲基化活性的厌氧细菌,在我们先前的工作中是从人肠道细菌中分离出来的。在这项研究中,枸杞E.limosum(1)ZL-II生物转化了水飞蓟黄素的成分,产生了四个新的转化产物-脱甲基异水飞蓟宾B(T1),脱甲基异水飞蓟宾A(T2),脱甲基水飞蓟宾B(T3)和脱甲基水飞蓟宾A( T4),其中T1和T2是新化合物。通过ESI-TOF / MS,H-1 NMR,C-13 NMR,HMBC和CD光谱数据鉴定了它们的化学结构。生物测定结果表明,转化产物T1-T4对阿兹海默氏淀粉样β42(A beta(2)(42))聚集表现出显着的抑制活性,IC50值为7.49μM-10.46μM,与之相当。阳性对照(表没食子儿茶素没食子酸酯,EGCG(3),为9.01μM),远低于其母体化合物的浓度(不少于145.10μM)。 E. limosum ZL-II进行生物转化的方法探索了一种从水飞蓟宾中开发新的,活性的铅化合物来治疗阿尔茨海默氏病的方法。然而,与它们的母体化合物相比,转化产物T1-T4对人肿瘤细胞系的抑制活性降低。

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