安普克
化学
激活剂(遗传学)
蛋白激酶A
AMP活化蛋白激酶
脂质代谢
药理学
铅化合物
葡萄糖稳态
生物化学
糖尿病
体外
内分泌学
激酶
胰岛素抵抗
受体
生物
作者
Yuusuke Tamura,Ippei Morita,Yu Hinata,Eiichi Kojima,Hiroki Ozasa,Hidaka Ikemoto,Mutsumi Asano,Toshihiro Wada,Yoko Hayasaki‐Kajiwara,Takanori Iwasaki,Ken‐ichi Matsumura
标识
DOI:10.1016/j.bmcl.2022.128769
摘要
AMP-activated protein kinase (AMPK) has been shown to play an important role in the beneficial effects of exercise on glucose and lipid metabolism in skeletal muscle and liver. Therefore, activation of AMPK has been proposed as an attractive strategy for the treatment of metabolic disorders, such as type 2 diabetes. Many of existing AMPK activators bearing diverse chemical structure were reported. However, there have been few reports of direct AMPK activator with high potency for β2-AMPK isoform, which is thought to be important for glucose homeostasis, and their chemical structure is limited to benzimidazole core. We describe herein our efforts for identification of novel AMPK activator. Our newly designed 4-azaindole derivative 16g exhibited single-digit nM in vitro activity, and chronic treatment with 16g led to dose-dependent improvement in HbA1c as well as decrease in hepatic lipid accumulation in diabetic animal model.
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