小檗碱
化学
罗格列酮
效力
二甲双胍
安普克
药理学
体外
免疫印迹
立体化学
生物化学
胰岛素
内分泌学
磷酸化
受体
蛋白激酶A
医学
基因
作者
Jianta Wang,Jin-Gang Peng,Jiquan Zhang,Zhongxiao Wang,Yi Zhang,Zhou Xingqin,Miao Jing,Lei Tang
标识
DOI:10.1016/j.bmcl.2019.126709
摘要
Four series of berberine derivatives were designed and synthesized. All the synthetic compounds were screened for in vitro glucose consumption activity in HepG2 cell lines. The results showed that most of the tested compounds exhibited potent hypoglycemic activity, and the most potent compound 20b exhibited its potency by 3.23-fold of berberine, 1.39-fold of metformin and 1.20-fold of rosiglitazone, respectively. Western blot assay indicated these novel berberine-based derivatives executed their glucose-decreasing activity via the activation of AMPK pathway.
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