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一种新的 6-烷氧基-[1,2,4]三唑并[4,3-b]哒嗪的合成及抗惊厥活性。

Synthesis and anticonvulsant activity of a new 6-alkoxy-[1,2,4]triazolo[4,3-b]pyridazine.

机构信息

School of Food, Drug & Medicine Zhejiang Ocean University, Zhoushan, Zhejiang Province 316004, PR China.

出版信息

Eur J Med Chem. 2010 May;45(5):1746-52. doi: 10.1016/j.ejmech.2009.12.077. Epub 2010 Jan 14.

Abstract

A series of 6-alkoxy-[1,2,4]triazolo[4,3-b]pyridazine derivatives were synthesized. In initial screening and quantitative evaluation, compound 2r was among the most active agents, exhibiting in the same time the lowest toxicity. In the anti-maximal electroshock test, it showed median effective dose (ED50) of 17.3 mg/kg and median toxicity dose (TD50) of 380.3 mg/kg, and the protective index (PI) of 22.0, which is much better than PI of the reference drugs. In a subsequent test, compound 2r had median hypnotic dose (HD50) of 746.6 mg/kg, thus demonstrating much better margin of safety compared to reference drugs. Compound 2r also showed oral activity against MES-induced seizures and lower oral neurotoxicity. For explanation of the putative mechanism of action, compound 2r was tested in chemical induced models.

摘要

合成了一系列 6-烷氧基-[1,2,4]三唑并[4,3-b]哒嗪衍生物。在初步筛选和定量评估中,化合物 2r 是最活跃的药物之一,同时表现出最低的毒性。在最大电休克试验中,它的半数有效剂量 (ED50) 为 17.3mg/kg,半数毒性剂量 (TD50) 为 380.3mg/kg,保护指数 (PI) 为 22.0,明显优于参比药物。在随后的试验中,化合物 2r 的催眠半数有效剂量 (HD50) 为 746.6mg/kg,与参比药物相比,安全性更好。化合物 2r 对 MES 诱导的癫痫发作也具有口服活性,且口服神经毒性较低。为了解释其可能的作用机制,对化合物 2r 进行了化学诱导模型的测试。

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