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PNU-120596

≥98%

N-(5-CHLORO-2,4-DIMETHOXYPHENYL)-N'-(5-METHYL-3-ISOXAZOLYL)-UREA

核磁下載

品牌：源葉(MedMol)

產(chǎn)品編號：S47640 一鍵復制產(chǎn)品信息

CAS號：501925-31-1

分子式：C₁₃H₁₄ClN₃O₄

分子量：311.72

MDL：MFCD00095313

別名：PNU120596 , PNU 120596 , NSC 216666 , 化合物PNU120596 , PNU120596 PNU 120596 NSC 216666

貨號	規(guī)格	價格	上海	北京	武漢	南京
S47640-10mg	≥98%	￥330.00 S47640-10mg ￥330.00 現(xiàn)貨	10 10	-	-	-
S47640-50mg	≥98%	￥680.00 S47640-50mg ￥680.00 現(xiàn)貨	6 6	-	-	-
S47640-100mg	≥98%	￥1300.00 S47640-100mg ￥1300.00 現(xiàn)貨	6 6	-	-	-

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產(chǎn)品介紹參考文獻質(zhì)檢證書(COA) 摩爾濃度計算器相關(guān)產(chǎn)品

產(chǎn)品介紹

PNU-120596 (NSC 216666) is a potent and selective α7 nAChR positive allosteric modulator (PMA) with an EC50 of 216 nM. PNU-120596 is inactive against α4β2, α3β4, and α9α10 nAChRs. PNU-120596 has the potential for psychiatric and neurological disorders research

產(chǎn)品描述：

靶點：

EC50: 216 nM (α7 nAChR);AChR

體外研究：

PNU-120596 increases agonist-evoked calcium flux mediated by an engineered variant of the human α7 nAChR. Electrophysiology studies confirme that PNU-120596 increases peak agonist-evoked currents mediated by wild-type receptors and also demonstrates a pronounced prolongation of the evoked response in the continued presence of agonist. PNU-120596 increases the channel mean open time of α7 nAChRs.
When applied to acute hippocampal slices, PNU-120596 increases the frequency of ACh-evoked GABAergic postsynaptic currents measured in pyramidal neurons.
PNU-120596 enhances agonist-evoked gating of nicotinic receptors by eliciting conformational effects that are similar but nonidentical to the gating conformations promoted by ACh.

體內(nèi)研究：

PNU-120596 (1 mg/kg; intravenous injection; once) treatment improves the auditory gating deficit caused by Amphetamine in rats, a model proposed to reflect a circuit level disturbance associated with schizophrenia.
When administered before carrageenan, NU-120596 (30 mg/kg; i.p.) significantly reduces mechanical hyperalgesia and weight-bearing deficits for up to 4 h in Sprague-Dawley rats. PNU-120596 attenuates the carrageenan-induced increase in levels of TNF-α and IL-6 within the hind paw oedema Animal Model: Male Sprague Dawley rats (250-300 g) treated with Amphetamine Dosage: 1 mg/kg Administration: Intravenous injection; once Result: Improved the auditory gating deficit caused by Amphetamine.

細胞實驗：

Cell lines: MCF7 和 Ishikawa 細胞 Concentrations: 1000 nM Incubation Time: 8天 Method: MCF7和Ishikawa細胞在10%三倍活性炭處理的包含血清的培養(yǎng)基中生長3天。然后細胞以2,000細胞/孔的密度接種在96孔組織培養(yǎng)板，并按照指示每48小時處理一次。使用CellTiter-Glo發(fā)光細胞活性試劑盒根據(jù)制造商方案第一次處理后，第8天，進行細胞增殖試驗

動物實驗：

Animal Models: 負荷 MCF-7 人乳腺腫瘤異種移植物的小鼠 Dosages: 8 mg/kg Administration: p.o.

參考文獻：

1. Hurst RS, et al. A novel positive allosteric modulator of the alpha7 neuronal nicotinic acetylcholine receptor: in vitro and in vivo characterization. J Neurosci, 2005, 25(17), 4396-4405.
2. Barron SC, et al. An allosteric modulator of alpha7 nicotinic receptors, N-(5-Chloro-2,4-dimethoxyphenyl)-N'-(5-methyl-3-isoxazolyl)-urea (PNU-120596), causes conformational changes in the extracellular ligand binding domain similar to those caused by acetylcholine. Mol Pharmacol, 2009 76(2), 253-263.
3. Munro G, et al. The α7 nicotinic ACh receptor agonist compound B and positive allosteric modulator PNU-120596 both alleviate inflammatory hyperalgesia and cytokine release in the rat. Br J Pharmacol, 2012, doi: 10.1111/j.1476-5381.2012.02003.x

溶解性：

Soluble in DMSO

保存條件：

-20℃

配置溶液濃度參考：

	1mg	5mg	10mg
1 mM	3.208 ml	16.04 ml	32.08 ml
5 mM	0.642 ml	3.208 ml	6.416 ml
10 mM	0.321 ml	1.604 ml	3.208 ml
50 mM	0.064 ml	0.321 ml	0.642 ml

注意：

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