首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Synthesis and evaluation of the anticonvulsant activity of 8-alkoxy-4,5-dihydrobenzo[b][1,2,4]triazolo[4,3-d][1,4]thiazepine derivatives
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Synthesis and evaluation of the anticonvulsant activity of 8-alkoxy-4,5-dihydrobenzo[b][1,2,4]triazolo[4,3-d][1,4]thiazepine derivatives

机译:8-烷氧基-4,5-二氢苯并[b] [1,2,4]三唑并[4,3-d] [1,4]硫氮平衍生物的合成及其抗惊厥活性

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摘要

Two series of 8-alkoxy-4,5-dihydrobenzo[b][1,2,4]triazolo[4,3-d][1,4] thiazepine derivatives (6a-q and 7a-q) were synthesized and evaluated for their anticonvulsant activity using the maximal electroshock (MES) method. All of the compounds prepared were effective in the MES screens. Among which, compound 7j was considered as the most promising one with an ED50 value of 26.3 mg/kg and a superior protective index value of 12.6. The potency of compound 7j against seizures induced by pentylenetetrazole, 3-mercaptopropionic acid and bicuculline suggested that two different mechanisms of action might potentially be involved in its anticonvulsant activity, including the inhibition of voltage-gated ion channels and the modulation of GABAergic activity. A computational study was also conducted to predict the pharmacokinetic properties of the compounds prepared, with the results supporting the use of these compounds as a group of promising antiepileptic agents.
机译:合成并评估了两个系列的8-烷氧基-4,5-二氢苯并[b] [1,2,4]三唑并[4,3-d] [1,4]硫氮平衍生物(6a-q和7a-q)使用最大电击(MES)方法测定其抗惊厥活性。制备的所有化合物在MES筛选中均有效。其中,化合物7j被认为是最有前途的化合物,ED50值为26.3 mg / kg,优越的保护指数值为12.6。化合物7j对抗戊四唑,3-巯基丙酸和双瓜氨酸诱发的癫痫发作的效力表明,其抗惊厥活性可能涉及两种不同的作用机制,包括抑制电压门控离子通道和调节GABA能活性。还进行了计算研究以预测所制备化合物的药代动力学性质,结果支持将这些化合物用作一组有希望的抗癫痫药。

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