节点文献
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
【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.
【Key words】 triazole; quinoline; [1,2,4]triazolo[4,3-a]quinoline; synthesis; anticonvulsant;
- 【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