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CNQX 115066-14-3

简要描述:CNQX 115066-14-3
CNQX (FG9065) 是高效的 AMPA/kainate 受体拮抗剂。

  • 产品型号:abs812835
  • 厂商性质:生产厂家
  • 更新时间:2026-02-26
  • 访  问  量:2605

详细介绍

品牌absinCAS115066-14-3
分子式C9H4N4O4纯度>98%
分子量232.15货号abs812835
规格10mg供货周期现货
主要用途是高效的 AMPA/kainate 受体拮抗剂。应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

CNQX 115066-14-3

产品描述
描述

 CNQX (FG9065) 是高效的 AMPA/kainate 受体拮抗剂。

纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
FG9065
可溶性/溶解性
DMSO: ≥30 mg/mL
生物活性
靶点
iGluR
In vitro(体外研究)
In rat hippocampal slices bathed in Mg2+-free medium, 10 μM CNQX reversibly blocks responses to a-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA), quisqualate and kainate but not NMDA. Superfusion of hippocampal slices with 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 2-5 μM) reversibly blocks the Schaffer collateral and mossy fibre excitatory postsynaptic potential (EPSP), while sparing the fast and slow GABA-mediated inhibition. CNQX (1-5 μM) produces a selective and dose-dependent reduction in the amplitude of the monosynaptic component of the DR-VRR recorded from lumbar spinal segments. CNQX-mediated depolarizations are mediated by AMPAR but not kainate receptors in TRN neurons.
In vivo(体内研究)
The bilateral infusion of CNQX (0.5 or 1.25 μg) into the amygdala or dorsal hippocampus 10 min prior to a retention test partially blocks the expression of stepdown inhibitory avoidance in rats 24 h after training. CNQX causes a complete blockade at a dose of 0.5 μg.
参考文献
参考文献
[1]. Blake JF, et al. CNQX blocks acidic amino acid induced depolarizations and synaptic components mediated by non-NMDA receptors in rathippocampal slices. Neurosci Lett. 1988 Jun 29;89(2):182-6.
[2]. Neuman RS, et al. Blockade of excitatory synaptic transmission by 6-cyano-7-nitroquinoxaline-2,3-dione(CNQX) in the hippocampus in vitro. Neurosci Lett. 1988 Sep 23;92(1):64-8.
[3]. Alford S, et al. CNQX and DNQX block non-NMDA synaptic transmission but not NMDA-evoked locomotion in lamprey spinal cord. Brain Res. 1990 Jan 8;506(2):297-302.
[4]. Lee SH, et al. Selective excitatory actions of DNQX and CNQX in rat thalamic neurons. J Neurophysiol. 2010 Apr;103(4):1728-34.
[5]. Kim M, et al. Infusion of the non-NMDA receptor antagonist CNQX into the amygdala blocks the expression of fear-potentiated startle. Behav Neural Biol. 1993 Jan;59(1):5-8.
研究领域
研究领域
Neuroscience
Drug DiscoverySmall Molecule DrugLead Compound Discovery
CNQX 115066-14-3温馨提示:本产品仅作科研实验使用,不支持临床等研究

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