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首页> 外文期刊>Letters in drug design & discovery >Synthesis and Anticonvulsant Activity of Novel 3-(2-(4H-1,2,4-triazol-4-yl)ethyl)-1-alkyl-1H-indole Derivatives
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Synthesis and Anticonvulsant Activity of Novel 3-(2-(4H-1,2,4-triazol-4-yl)ethyl)-1-alkyl-1H-indole Derivatives

机译:新型3-(2-(2-(4H-1,2,4-三唑-4-基)乙基)-1-烷基-1H-吲哚衍生物的合成和抗惊厥活性

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摘要

A series of novel 3-[2-(4H-1,2,4-triazol-4-yl) ethyl]-1-alkyl-1H-indole derivatives (4a-s) were synthesized and evaluated for their anticonvulsant activity and neurotoxicity by using maximal electroshock (MES) and rotarod neurotoxicity (TOX) tests. Among the compounds studied, compound 3-[2-(4H-1,2,4-triazol-4-yl) ethyl]-1-nonyl-1H-indole (4p) was found by intraperitoneal (i.p.) administration in mice to be the most potent compound with a median effective dose (ED50) value of 10.2 mg/kg, possessed better anticonvulsant activity and higher safety than carbamazepine.
机译:合成了一系列新型的3- [2-(4H-1,2,4-三唑-4-基)乙基] -1-烷基-1H-吲哚衍生物(4a-s),并对其抗惊厥活性和神经毒性进行了评估通过使用最大电击(MES)和轮状神经毒性(TOX)测试。在研究的化合物中,通过在小鼠腹膜内(ip)给药发现了化合物3- [2-(4H-1,2,4-三唑-4-基)乙基] -1-壬基-1H-吲哚(4p)。是最有效的化合物,中位有效剂量(ED50)值为10.2 mg / kg,比卡马西平具有更好的抗惊厥活性和更高的安全性。

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