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Potent SIRT1 Enzyme-stimulating and Anti-glycation Activities of Polymethoxyflavonoids from Kaempferia parviflora

机译:短小Kaempferia parviflora的多甲氧基类黄酮对SIRT1的强效酶促和抗糖化作用

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摘要

The SIRT1 enzyme-stimulating and anti-glycation activities of Kaempferia parviflora extract and its main polymethoxyflavonoids were evaluated in vitro. K parviflora extract elevated SIRT1 catalytic activity by eight- and 17-fold at 20 mu g/mL and 100 mu g/mL, respectively, compared with vehicle only. Two major polymethoxyflavonoids, 3,5,7,3',4'-pentamethoxyflavone (4) and 5,7,4'-trimethoxyflavone (5), were isolated from this extract and are four- and fivefold more potent than resveratrol, hitherto the strongest known natural SIRT1 activator. In addition, the anti-glycation activity of K parviflora extract was observed to be seven times more effective than aminoguanidine, a clinical anti-diabetes drug. 3,5,7,3',4'-Pentamethoxyflavone (4) and 5,7,4'-trimethoxyflavone (5) showed the strongest anti-glycation activity among the tested polymethoxyflavonoids. Further comparison of the activity of these structurally related polymethoxyflavonoids revealed a possible structure-activity relationship, in particular, for the contribution of methoxy moieties.
机译:在体外评估了Kaempferia parviflora提取物及其主要聚甲氧基类黄酮的SIRT1酶刺激和抗糖基化活性。与仅用赋形剂相比,K小花提取物在20μg / mL和100μg / mL下分别将SIRT1催化活性提高了8倍和17倍。从该提取物中分离出两种主要的聚甲氧基黄酮类化合物3,5,7,3',4'-五甲氧基黄酮(4)和5,7,4'-三甲氧基黄酮(5),迄今为止的效力比白藜芦醇高四到五倍。最强的已知天然SIRT1激活剂。此外,观察到小花K提取物的抗糖化活性比临床抗糖尿病药物氨基胍有效七倍。 3,5,7,3',4'-五甲氧基黄酮(4)和5,7,4'-三甲氧基黄酮(5)在测试的聚甲氧基类黄酮中显示出最强的抗糖化活性。这些结构相关的聚甲氧基黄酮类化合物的活性的进一步比较揭示了可能的结构-活性关系,特别是对于甲氧基部分的贡献。

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