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设计和合成芳脒衍生物作为 5-羟色胺/去甲肾上腺素双重再摄取抑制剂。

Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors.

机构信息

Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.

National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.

出版信息

Molecules. 2019 Jan 30;24(3):497. doi: 10.3390/molecules24030497.

Abstract

To improve the in vivo antidepressant activity of previously reported serotonin (5-HT) and norepinephrine (NE) dual reuptake inhibitors, three series of arylamidine derivatives were designed and synthesized. The in vitro 5-HT and NE reuptake inhibitory activities of these compounds were evaluated, and compound was identified as the most potent 5-HT (IC = 620 nM) and NE (IC = 10 nM) dual reuptake inhibitor. Compound exhibited potent antidepressant activity in the rat tail suspension test and showed an acceptable safety profile in a preliminary acute toxicity test in mice. Our results show that these arylamidine derivatives exhibit potent 5-HT/NE dual reuptake inhibition and should be explored further as antidepressant drug candidates.

摘要

为了提高先前报道的 5-羟色胺(5-HT)和去甲肾上腺素(NE)双重再摄取抑制剂的体内抗抑郁活性,设计并合成了三系列芳脒衍生物。评估了这些化合物的体外 5-HT 和 NE 再摄取抑制活性,发现化合物 是最有效的 5-HT(IC = 620 nM)和 NE(IC = 10 nM)双重再摄取抑制剂。化合物 在大鼠悬尾试验中表现出较强的抗抑郁活性,在小鼠初步急性毒性试验中表现出可接受的安全性特征。我们的结果表明,这些芳脒衍生物表现出较强的 5-HT/NE 双重再摄取抑制作用,应该作为抗抑郁药物候选物进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b17/6385122/999b7305ab17/molecules-24-00497-g001.jpg

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