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新型苯并氮杂䓬酮衍生物作为具有强效活性的糖原磷酸化酶抑制剂的发现与评价

Discovery and evaluation of novel benzazepinone derivatives as glycogen phosphorylase inhibitors with potent activity.

作者信息

Wang Youde, Yan Zhiwei, Guo Yachun, Zhang Liying

机构信息

Key Laboratory of Traditional Chinese Medicine Research & Development of Hebei Province, Institute of Traditional Chinese Medicine, Chengde Medical University, Chengde, 067000, China.

Department of Pathogen Biology, Chengde Medical University, Chengde, Hebei, 067000, China.

出版信息

Future Med Chem. 2021 May;13(10):897-909. doi: 10.4155/fmc-2020-0352. Epub 2021 Apr 28.

Abstract

Glycogen phosphorylase (GP) is a key enzyme of glycogen catabolism, so it is significant to discover a new GP inhibitor. A series of benzazepinone derivatives were discovered as GP inhibitors with potent activity. Among these derivatives, compound showed significant potential against rabbit muscle GPa (IC = 0.25 ± 0.05 μM) and cellular efficacy. The study revealed that significantly inhibited increases in fasting blood glucose level in two kinds of hyperglycemic mice models. The possible binding mode of compound was explored based on molecular docking simulations. These results indicated that derivatives with benzazepinone were potential chemical entities against hyperglycemia.

摘要

糖原磷酸化酶(GP)是糖原分解代谢的关键酶,因此发现一种新的GP抑制剂具有重要意义。一系列苯并氮杂䓬酮衍生物被发现是具有强效活性的GP抑制剂。在这些衍生物中,化合物对兔肌肉GPa表现出显著的潜力(IC = 0.25±0.05μM)和细胞功效。该研究表明,在两种高血糖小鼠模型中,该化合物显著抑制空腹血糖水平的升高。基于分子对接模拟探索了该化合物可能的结合模式。这些结果表明,苯并氮杂䓬酮衍生物是对抗高血糖的潜在化学实体。

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