首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis and Antihyperglycemic Activity of [2-(Substituted phenyl)-3-[{4-(1-naphthyl)-1,3-thiazol- 2-yl}amino]-4-oxo-1,3-thiazoIidin-5-yl] Acetic Acid
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Synthesis and Antihyperglycemic Activity of [2-(Substituted phenyl)-3-[{4-(1-naphthyl)-1,3-thiazol- 2-yl}amino]-4-oxo-1,3-thiazoIidin-5-yl] Acetic Acid

机译:[2-(取代的苯基)-3-[{4-(1-萘基)-1,3-噻唑-2-基}氨基] -4-氧代-1,3-噻唑烷-5-的合成及降血糖活性[yl]乙酸

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The title compounds were prepared by brominating 1 -acetyl naphthalene in chloroform followed by condensation with substituted benzaldehyde thiosemicarbazones using ethanol to get 4-(1-naphthyl)-2-(substituted benzylidineamino)-1,3-thiazoles. These thiazole derivatives were then cyclized to title compounds by reacting with thiomalic acid in dioxane using ZnCl2. All the synthesized compounds were characterized on the basis of their IR, ~1H NMR, mass and elemental analysis. The antihyperglycemic study was divided into two phases. Phase-I involved evaluation of blood glucose lowering ability of thiazolidinones in normal rats by sucrose loaded model (SLM). It was observed that compound with Ar = 4-nitro-phenyl displayed highest antihyperglycemic activity in SLM. Phase-II study included the evaluation of blood sugar by alloxan model. It was observed that most of the compounds exhibited more antihyperglycemic activity than standard drug pioglitazone on 7th day of study. It was also observed that blood glucose lowering effects were more pronounced and stronger in alloxan model.
机译:通过将1-乙酰基萘在氯仿中溴化,然后使用乙醇与取代的苯甲醛硫代半氨基甲酮缩合,得到4-(1-萘基)-2-(取代的苄基氨基)-1,3-噻唑,来制备标题化合物。然后通过使用ZnCl2与硫代苹果酸在二恶烷中反应,将这些噻唑衍生物环化为标题化合物。所有合成的化合物均通过IR,〜1H NMR,质量和元素分析进行​​表征。降血糖研究分为两个阶段。 I期涉及通过蔗糖加载模型(SLM)评估正常大鼠中噻唑烷酮的降血糖能力。观察到在SLM中Ar = 4-硝基-苯基的化合物显示出最高的降血糖活性。 II期研究包括通过四氧嘧啶模型评估血糖。在研究的第7天,观察到大多数化合物比标准药物吡格列酮具有更高的降血糖活性。还观察到在四氧嘧啶模型中,降低血糖的作用更明显并且更强。

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