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α-Glucosidase Inhibitory Activity of Kaempferol-3-O-rut?noside

机译:山茱fer醇-3-O-芸香糖苷的α-葡萄糖苷酶抑制活性

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摘要

Quercetin, kaempferol and to a lesser extent rutin have been reported to have antidiabetic activities when assessed by various assay models including in vitro α-glucosidase inhibition studies. A related structural analogue, kaempferol-3-O-rut?noside (KR) however has not yet been studied for such biological effects. It was found that KR is a potent inhibitor of α-glucosidase in vitro with over 8-times more activity than the reference antidiabetic drug, acarbose. Furthermore, KR displayed a synergistic effect with a less potent flavonoid aglycones, kaempferol and quercetin. The structure-activity profile of these drugs and implications of drug combinations are discussed.
机译:当通过包括体外α-葡萄糖苷酶抑制研究在内的各种测定模型评估时,槲皮素,山奈酚和较小程度的芦丁具有抗糖尿病活性。相关的结构类似物,kaempferol-3-O-rut?noside(KR)尚未针对这种生物学效应进行过研究。已发现KR是一种有效的α-葡萄糖苷酶体外抑制剂,其活性是参考抗糖尿病药物阿卡波糖的8倍以上。此外,KR与低效的类黄酮苷元,山奈酚和槲皮素具有协同作用。讨论了这些药物的结构活性概况以及药物组合的意义。

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