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2-(1-Piperazinyl)pyrimidine
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。
2-(1-Piperazinyl)pyrimidine图片
规格:98%
分子量:164.2
包装与价格:
包装价格(元)
10g询价
25g询价
50g询价
100g询价

An α2-AR antagonist and active metabolite of azapirones
货号:ajcx25296
CAS:20980-22-7
分子式:C8H12N4
分子量:164.2
溶解度:DMF: 10mg/ml,DMSO: 10mg/ml,Ethanol: 10mg/ml,PBS (pH 7.2): 10mg/ml
纯度:98%
存储:Store at -20°C
库存:现货

Background:

2-(1-Piperazinyl)pyrimidine is an antagonist of α2-adrenergic receptors (α2-ARs; pA2= 6.8 in rat brain synaptosomes) and active metabolite of various azapirones, including buspirone.1,2,3,4It is formed from buspirone by the cytochrome P450 (CYP) isoform CYP3A4 in human liver microsomes.52-(1-Piperazinyl)pyrimidine inhibits decreases in gastrointestinal transit induced by clonidine in rats (ED50= 0.8 mg/kg).2It increases drinking in the Vogel punished drinking task, indicating anxiolytic-like activity, in rats when administered at doses ranging from 1 to 4 mg/kg.32-(1-Piperazinyl)pyrimidine (0.25-1 mg/kg) also reduces the amplitude of electrically stimulated excitatory post-synaptic potentials (EPSPs) in the hippocampal CA1 region in rats, an effect that can be blocked by the serotonin (5-HT) receptor subtype 5-HT1Aantagonist spiroxatrine.4It has also been used a phosphopeptide derivatization agent.6


1.Gobbi, M., Frittoli, E., and Mennini, T.Antagonist properties of 1-(2-pyrimidinyl)piperazine at presynaptic α2-adrenoceptors in the rat brainEur. J. Pharmacol.180(1)183-186(1990) 2.Bianchi, G., Caccia, S., Della Vedova, F., et al.The α2-adrenoceptor antagonist activity of ipsapirone and gepirone is mediated by their common metabolite 1-(2-pyrimidinyl)-piperazine (PmP)Eur. J. Pharmacol.151(3)365-371(1988) 3.Gower, A.J., and Tricklebank, M.D.α2-adrenoceptor antagonist activity may account for the effects of buspirone in an anticonflict test in the ratEur. J. Pharmacol.155(1-2)129-137(1988) 4.Manahan-Vaughan, D., Anwyl, R., and Rowan, M.J.The azapirone metabolite 1-(2-pyrimidinyl)piperazine depresses excitatory synaptic transmission in the hippocampus of the alert rat via 5-HT1A receptorsEur. J. Pharmacol.294(2-3)617-624(1995) 5.Zhu, M., Zhao, W., Jimenez, H., et al.Cytochrome P450 3A-mediated metabolism of buspirone in human liver microsomesDrug Metab. Dispos.33(4)500-507(2005) 6.Zhang, L., Xu, Y., Lu, H., et al.Carboxy group derivatization for enhanced electron-transfer dissociation mass spectrometric analysis of phosphopeptidesProteomics9(16)4093-4097(2009)

 
 
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