Synthesis and anticonvulsant activity of 7-benzylamino-4, 5dihydro-[1,2,4] triazolo[4,3-a]quinolines

被引:0
作者
Cui Xiangshu
Guan Liping
Li Hailan
Piao Huri
Quart Zheshan [1 ]
机构
[1] Yanbian Univ, Minist Educ, Key Lab Organ Funct Factors Changbai Mt, Yanji 133002, Peoples R China
[2] Yanbian Univ, Coll Basic Med, Yanji 133000, Peoples R China
[3] Yanbian Univ, Coll Pharm, Yanji 133000, Peoples R China
关键词
quinoline; triazole; synthesis; anticonvulsant; epilepsia;
D O I
暂无
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series of 7-substituted-benzylamino-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline derivatives was synthesized and evaluated for their anticonvulsant activity. The subcutaneous pentylenetetrazole test (sc-PTZ) demonstrated that the most effective compound in controlling the sc-PTZ induced seizure was 7-(3-bromine-benzylamino)-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline (4j) with an ED50 of 5.0 mg/kg and the PI of 20.7, which was also safer than the reference drugs. And the maximal electroshock test (MES) demonstrated that among these derivatives, 7-(3-fluorobenzylamino) -4, 5-dihydro-[ 1, 2, 4]trizolo[4, 3-a]quinoline (4i), with an ED50 of 15.3 mg/kg and the PI of 7.2, was the safest in MES test. Furthermore, their neurotoxicities were measured by the rotated neurotoxicity test, and the results showed that all derivatives possessed lower neurotoxicity.
引用
收藏
页码:1104 / 1108
页数:5
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