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RO5166017
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。
RO5166017图片
规格:98%
分子量:219.3
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议

产品介绍
RO5166017 是一种具有口服活性的跨物种 TAAR1 激动剂,对小鼠、大鼠、人和食蟹猴的 Ki 值分别为 1.9 nM、2.7 nM、31 nM 和 24 nM。
货号:ajcx24828
CAS:1048346-74-2
分子式:C12H17N3O
分子量:219.3
溶解度:DMF: 30 mg/ml,DMF:PBS (pH 7.2) (1:2): 0.33 mg/ml,DMSO: 10 mg/ml,Ethanol: 10 mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

RO5166017 is an agonist of trace amine-associated receptor 1 (TAAR1).1It binds to TAAR1 (Kis = 31, 24, 1.9, and 2.7 nM in HEK293 cells expressing the recombinant human, cynomolgus monkey, mouse, or rat receptor, respectively) and is greater than 15-fold selective for TAAR1 over a panel of 123 receptors, ion channels, and transporters at 10 µM. RO5166017 induces cAMP production in HEK293 cells expressing the recombinant human, cynomolgus monkey, mouse, or rat TAAR1 (EC50s = 55, 97, 3.3, and 14 nM, respectively). It reduces the frequency of neuronal firing in mouse ventral tegmental area (VTA) and dorsal raphe nucleus (DRN) slices (IC50s = 1.73 and 2.99 nM, respectively), which endogenously express high levels of dopaminergic and serotonergic neurons, respectively. RO5166017 (0.3 mg/kg) inhibits stress-induced hyperthermia, indicating anxiolytic-like activity, as well as reduces cocaine-induced hyperlocomotion, in mice. It also impairs expression, but not reconsolidation, of cocaine-induced place preference in rats.2


1.Revel, F.G., Moreau, J.-L., Gainetdinov, R.R., et al.TAAR1 activation modulates monoaminergic neurotransmission, preventing hyperdopaminergic and hypoglutamatergic activityProc. Natl. Acad. Sci. USA108(20)8485-8490(2011) 2.Liu, J.-F., Thorn, D.A., Zhang, Y., et al.Effects of trace amine-associated receptor 1 agonists on the expression, reconsolidation, and extinction of cocaine reward memoryInt. J. Neuropsychopharmacol.19(7)pyw009(2016)