新型氨基磺酰苯酰胺衍生物葡萄糖激酶活化剂的设计、合成及降糖活性研究

A. Grewal, K. Sharma, Sukhbir Singh, Vikramjeet Singh, D. Pandita, Viney Lather
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引用次数: 8

摘要

本研究计划设计、合成和评价一系列磺胺酰苄酰胺衍生物作为潜在的葡萄糖激酶(GK)活化剂的降糖潜力。以3-硝基苯甲酸为起始原料合成了一系列新的磺胺酰苯酰胺衍生物,并对其进行了表征。进行了硅对接研究,以确定GK酶变构位点上最合适构象的结合相互作用。基于计算机实验的结果,在动物实验(四氧嘧啶诱导的糖尿病动物模型)中测试了所选分子的抗糖尿病活性。化合物7在动物实验中表现出最高的抗糖尿病活性。体内抗糖尿病活性研究的结果与对接研究的结果一致。因此,这些新合成的磺胺酰苯酰胺衍生物可以作为开发新型、安全、有效和口服生物可利用的GK活化剂作为治疗2型糖尿病的治疗剂的初始目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design, Synthesis and Antidiabetic Activity of Novel Sulfamoyl Benzamide Derivatives as Glucokinase Activators
The present work has been planned to design, synthesize and evaluate the antidiabetic potential of a series of sulfamoyl benzamide derivatives as potential glucokinase (GK) activators. A new series of sulfamoyl benzamide derivatives was synthesized starting from 3-nitrobenzoic acid and characterized. In silico docking studies were performed to determine the binding interactions for the best fit conformations in the allosteric site of GK enzyme. Based on the results of in silico studies, the selected molecules were tested for their antidiabetic activity in animal studies (alloxan induced diabetic animal model). Compound 7 exhibited highest antidiabetic activity in animal studies. The results of in vivo antidiabetic activity studies were found to be in parallel to that of docking studies. These newly synthesized sulfamoyl benzamide derivatives thus can be treated as the initial hits for the development of novel, safe, effective and orally bioavailable GK activators as therapeutic agents for the treatment of type 2 diabetes.
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