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Synthesis and in vivo hypoglycemic activity of new imidazolidine-2,4-dione derivatives

机译:新型咪唑烷-2,4-二酮衍生物的合成及体内降血糖活性

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A series of new 3-arylsulfonylimidazolidine-2,4-diones (2a-2p) were synthesized by reacting imidazolidine-2,4-diones (1a-1e) with arylsulfonyl chlorides in the presence of triethyl amine. The imidazolidine-2,4-diones (1a-1e) were in turn synthesized from the corresponding ketones through Bucherer-Bergs reaction. All the synthesized compounds were characterized on the basis of their spectral (IR, H-1 and C-13 NMR and MS) and microanalytical data. The hypoglycemic activity of the compounds (2a-2p) was evaluated using alloxanized diabetic rat model. Compound 2a showed an excellent activity with a reduction in the blood glucose level of -286 +/- A 7 mg/dL after 5 h of drug administration as compared to -270 +/- A 8 mg/dL for glipizide. The hypoglycemic activity of compound 2b (-268 +/- A 9 mg/dL) was also comparable to the standard drug. However, only moderate activity was observed for compound 2e.
机译:在三乙胺存在下,通过使咪唑烷-2,4-二酮(1a-1e)与芳基磺酰氯反应,合成了一系列新的3-芳基磺酰亚胺基咪唑-2,4-二酮(2a-2p)。然后通过Bucherer-Bergs反应由相应的酮合成咪唑烷-2,4-二酮(1a-1e)。所有合成的化合物都根据其光谱(IR,H-1和C-13 NMR和MS)和微分析数据进行表征。使用脲醛化的糖尿病大鼠模型评估化合物(2a-2p)的降血糖活性。与格列吡嗪的-270 +/- A 8 mg / dL相比,给药2小时后,化合物2a表现出优异的活性,血糖水平降低了-286 +/- A 7 mg / dL。化合物2b的降血糖活性(-268 +/- A 9 mg / dL)也与标准药物相当。然而,对于化合物2e仅观察到中等活性。

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