首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Synthesis and hypoglycemic activity of some new theophylline derivatives
【24h】

Synthesis and hypoglycemic activity of some new theophylline derivatives

机译:一些新的茶碱衍生物的合成和降血糖活性

获取原文
获取原文并翻译 | 示例
           

摘要

Thirty-one new theophylline derivatives have been synthesized and evaluated for their hypoglycemic activity. Compounds 24 (56% reduction) and 31 (57% reduction) showed better hypoglycemic activity than the standard drug glibenclamide which showed 52% reduction in serum glucose level. Compound 27 remarkably reduced serum glucose level by 53%. Ten compounds showed varying degrees of hypoglycemic activity ranging from 20 to 37% reduction in serum glucose level compared to the standard drug. The aromatic amide functionality is the common feature of these theophylline hypoglycemic derivatives. However, anthranilamide and or aliphatic amides proved to be the least active compounds in the present series.
机译:已经合成了三十一点新鲜的蛋白衍生物,并评估其降血糖活动。 化合物24(减少56%)和31(减少57%)显示出比标准药物Glibenclamide更好的降血糖活性,所述药物Glibenclamide显示出血清葡萄糖水平的52%。 化合物27使血清葡萄糖水平显着降低53%。 与标准药物相比,十种化合物显示出血清葡萄糖水平的20%至37%的降低程度。 芳族酰胺功能是这些低钙碱衍生物的常见特征。 然而,苯胺酰胺和或脂族酰胺被证明是本系列中最不活性化合物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号