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Agomelatine
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Agomelatine图片
CAS NO:138112-76-2
包装与价格:
包装价格(元)
10mM (in 1mL DMSO)电议
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
Agomelatine (S-20098) 是 MT1 和 MT2 受体的特异性激动剂,对 CHO-hMT1、HEK-hMT1、CHO-hMT2 和 HEK-hMT2 的 Kis 分别为 0.1、0.06、0.12 和 0.27 nM。
Cas No.138112-76-2
别名阿戈美拉汀; S-20098
化学名N-[2-(7-methoxynaphthalen-1-yl)ethyl]acetamide
Canonical SMILESCC(=O)NCCC1=CC=CC2=C1C=C(C=C2)OC
分子式C15H17NO2
分子量243.3
溶解度≥ 12.2mg/mL in DMSO
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

Agomelatine is an agonist of melatonin receptors and an antagonist of the serotonin 5-HT2C receptor with Ki values of 0.062nM and 0.268nM and IC50 value of 0.27μM, respectively for MT1, MT2 and 5-HT2C [1].

Agomelatine is a unique antidepressant and is developed for treatment of major depressive disorder (MDD). Agomelatine is selective against 5-HT2C. It shows low affinities to cloned human 5-HT2A and 5-HT1A. For melatonin receptors, agomelatine shows similar affinities to cloned human MT1 and MT2 with Ki values of 0.09nM and 0.263nM, respectively. In the in vivo studies, agomelatine causes increase of dopamine and noradrenaline levels via blocking the inhibitory input of 5-HT2C. Moreover, the administration of agomelatine counteractes the stress-induced decrease in sucrose consumption in a rat model of depression. Besides that, agomelatine exerts alleviated anxiety efficacy in a rodent model of anxiety [1].

References:
[1] Zupancic M, Guilleminault C. Agomelatine. CNS drugs, 2006, 20(12): 981-992.