木犀草素
阿卡波糖
餐后
化学
α-葡萄糖苷酶
类黄酮
效力
α-淀粉酶
药理学
大豆黄酮
生物化学
医学
胰岛素
体外
淀粉酶
酶
内科学
染料木素
抗氧化剂
作者
Jong‐Sang Kim,Chong-Suk Kwon,Kun Ho Son
摘要
Twenty-one naturally occurring flavonoids were tested for inhibitory activities against alpha-glucosidase (EC 3.2.1.20) and alpha-amylase (EC 3.2.1.1). Luteolin, amentoflavone, luteolin 7-O-glucoside, and daidzein were the strongest inhibitors among the compounds tested. Luteolin inhibited alpha-glucosidase by 36% at the concentration of 0.5 mg/ml and was stronger than acarbose, the most widely prescribed drug, in inhibitory potency, suggesting that it has the possibility to effectively suppress postprandial hyperglycemia in patients with non-insulin dependent diabetes mellitus. Luteolin also inhibited alpha-amylase effectively although it was less potent than acarbose. The clinical value of luteolin needs to be further evaluated.
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