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α-细辛脑衍生物的合成、抗癫痫作用及构效关系:部分衍生物的体外和体内神经保护作用。

Synthesis, antiepileptic effects, and structure-activity relationships of α-asarone derivatives: In vitro and in vivo neuroprotective effect of selected derivatives.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

Key Laboratory of Drug Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

出版信息

Bioorg Chem. 2021 Oct;115:105179. doi: 10.1016/j.bioorg.2021.105179. Epub 2021 Jul 15.

Abstract

In the present study, we compared the antiepileptic effects of α-asarone derivatives to explore their structure-activity relationships using the PTZ-induced seizure model. Our research revealed that electron-donating methoxy groups in the 3,4,5-position on phenyl ring increased antiepileptic potency but the placement of other groups at different positions decreased activity. Besides, in allyl moiety, the optimal activity was reached with either an allyl or a 1-butenyl group in conjugation with the benzene ring. The compounds 5 and 19 exerted better neuroprotective effects against epilepsy in vitro (cell) and in vivo (mouse) models. This study provides valuable data for further exploration and application of these compounds as potential anti-seizure medicines.

摘要

在本研究中,我们比较了α-细辛脑衍生物的抗癫痫作用,以使用 PTZ 诱导的癫痫模型来探索它们的构效关系。我们的研究表明,苯基环上 3、4、5 位的供电子甲氧基增加了抗癫痫效力,但在不同位置放置其他基团则降低了活性。此外,在烯丙基部分,与苯环共轭的烯丙基或 1-丁烯基具有最佳的活性。化合物 5 和 19 在体外(细胞)和体内(小鼠)癫痫模型中表现出更好的神经保护作用。这项研究为进一步探索和应用这些化合物作为潜在的抗癫痫药物提供了有价值的数据。

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