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7-取代苯氧基-4,5-二氢-1,2,4-三唑并[4,3-a]喹啉和喹啉-1(2H)-酮衍生物的合成及抗惊厥活性

Synthesis and Anticonvulsant Activity Study of 7-Substituted Phenoxyl-4,5-dihydro[1,2,4]triazolo[4,3-a]quinolines and Quinoline-1(2H)-ones

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【作者】 金云哲关丽萍赵立明朴虎日全哲山

【Author】 JIN, Yun-Zhea,b GUAN, Li-Pingb ZHAO, Li-Mingb PIAO, Hu-Rib QUAN, Zhe-Shan*,a,b (a Key Laboratory of Organism Functional Factors of the Changbai Mountain, Ministry of Education, Yanbian University, Yanji 133002) (b College of Pharmacy, Yanbian University, Yanji 133000)

【机构】 延边大学长白山生物功能因子省部共建教育部重点实验室延边大学药学院延边大学长白山生物功能因子省部共建教育部重点实验室 延吉133002延边大学药学院延吉133000延吉133000延吉133002延边大学药学院延吉133000

【摘要】 合成了7-取代苯氧基-4,5-二氢-1,2,4-三唑并[4,3-a]喹啉(3a~3g)和7-取代苯氧基-4,5-二氢-1,2,4-三唑并[4,3-a]喹表明啉-1(2H)-酮(4a~4g)类衍生物.以最大电惊厥法和戊四唑法测定了抗惊厥活性,以旋转棒法测定了神经毒性.结果表明,化合物7-(4-氟苯氧基)-4,5-二氢-1,2,4-三唑并[4,3-a]喹啉-1(2H)-酮(4c)显示最强的抗惊厥作用和低的神经毒性,其抗电惊厥ED50为6.8mg/kg,神经毒性TD50为88.0mg/kg,保护指数PI为12.9,明显优于对照药苯妥英钠.

【Abstract】 A series of 7-(substituted phenoxyl)-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinolines and 7-(substi-tuted phenoxyl)-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline-1(2H)-ones were synthesized. The convulsant effect and neurotoxicity of the compound were determined with maximal electroshock test (MES), penty-lenetetrazol (PTZ) method and rotarod test intraperitoneally in mice. 7-(4-Fluorophenyloxy)-4,5-dihy-dro-[1,2,4]triazolo[4,3-a]quinoline-1(2H)-one (4c) was the most active and also has the lowest toxicity. In the anti-MES potency test, 4c showed a medial effective dose (ED50) of 6.8 mg/kg, a medial toxicity dose (TD50) of 88.0 mg/kg, and the protective index (PI) of 12.9. The PI value of compound 4c was better than that of the marketed drug phenytoin.

【基金】 国家自然科学基金(No.30460151);教育部重点(No.2007-24)资助项目.
  • 【文献出处】 有机化学 ,Chinese Journal of Organic Chemistry , 编辑部邮箱 ,2007年12期
  • 【分类号】O626
  • 【被引频次】14
  • 【下载频次】261
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