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| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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| 描述 | CNQX (FG9065) is a potent and competitive AMPA/kainate receptor antagonist with IC50s of 0.3 μM and 1.5 μM, respectively. CNQX is a competitive non-NMDA receptor antagonist[1]. Superfusion of hippocampal slices with 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 2-5 microM) reversibly blocked the Schaffer collateral and mossy fibre excitatory postsynaptic potential (EPSP), while sparing the fast and slow gamma-aminobutyric acid (GABA)-mediated inhibition. CNQX may be a useful antagonist to study excitatory amino acid-mediated synaptic transmission[2]. 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. The activation of NMDA receptors is sufficient to elicit and maintain fictive locomotion after blockade of non-NMDA receptors with either DNQX or CNQX[3]. |
| Concentration | Treated Time | Description | References | |
| mouse cerebellar Purkinje cells | 40 μM | CNQX completely blocked the rapid EPSC | Neuron. 2008 Aug 14;59(3):392-8 | |
| mouse cerebellar Purkinje cells | 10 μM | CNQX reduced the amplitude of the rapid EPSC by about 90% | Neuron. 2008 Aug 14;59(3):392-8 | |
| pTRG neurons | 50 μM | CNQX and AP5 greatly reduced the EPSCs induced by MLR stimulation | Proc Natl Acad Sci U S A. 2012 Jan 10;109(2):E84-92 | |
| respiratory motoneurons | 1 mM | CNQX and AP5 significantly reduced the area of EPSPs induced by MLR stimulation | Proc Natl Acad Sci U S A. 2012 Jan 10;109(2):E84-92 | |
| GluA1 AMPARs | 100 nM | To study the inhibitory effect of CNQX on GluA1 AMPARs | J Physiol. 2011 Nov 15;589(Pt 22):5383-90 | |
| tsA201 cells | 100 nM | To study the inhibitory effect of CNQX on GluA1 AMPARs | J Physiol. 2011 Nov 15;589(Pt 22):5383-90 | |
| Layer V pyramidal neurons in rat prefrontal cortex slices | 30 µM | To test the effect of CNQX on 5-HT-induced synaptic activity. Results showed that CNQX completely blocked the increase in synaptic activity induced by 5-HT | J Physiol. 2004 May 1;556(Pt 3):739-54 |
| Administration | Dosage | Frequency | Description | References | ||
| Lampreys | Semi-intact preparations | Local injections | 1 mM | Blockade of excitatory transmission in the dorsal MLR markedly reduced the respiratory increases associated with locomotion | Proc Natl Acad Sci U S A. 2012 Jan 10;109(2):E84-92 | |
| Rat | Anesthetized rats | Local application | 20 μM | Single application | Inhibited spontaneous EPSCs | J Physiol. 2012 May 15;590(10):2225-31 |
| Rats | Water maze test | Bilateral intra-LHb infusion | 267 ng/side | Single injection, behavioral testing performed 15 minutes post-injection | To investigate the role of LHb in encoding and retrieval of spatial memory. Results showed that CNQX infusion prevented encoding and retrieval, but not consolidation of spatial information. | Neuropsychopharmacology. 2015 Nov;40(12):2843-51 |
| Cats | Vestibulo-ocular reflex (VOR) model | Bilateral cerebellar cortex injection | 3 mM,5–20 μl | Single injection, lasting 20 minutes | To investigate the effect of CNQX blockade of excitatory neurotransmission in the cerebellar cortex on VOR gain. Results showed complete reversal of short-term memory expression and only partial effect on long-term memory expression. | J Neurosci. 2005 Aug 31;25(35):7979-85 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
4.31mL 0.86mL 0.43mL |
21.54mL 4.31mL 2.15mL |
43.07mL 8.61mL 4.31mL |
|
| CAS号 | 115066-14-3 |
| 分子式 | C9H4N4O4 |
| 分子量 | 232.16 |
| SMILES Code | [O-][N+](=O)C1=C(C=C2NC(=O)C(=O)NC2=C1)C#N |
| MDL No. | MFCD00069232 |
| 别名 | |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, store in freezer, under -20°C |
| 溶解方案 |
DMSO: 18 mg/mL(77.53 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
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