推荐产品
product name
NBQX 二钠盐 水合物, ≥98% (HPLC)
品質等級
化驗
≥98% (HPLC)
形狀
lyophilized powder
儲存條件
desiccated
顏色
, brown to dark red-brown
溶解度
H2O: >10 mg/mL
儲存溫度
2-8°C
SMILES 字串
O.[Na+].[Na+].NS(=O)(=O)c1cccc2c1c(cc3nc([O-])c([O-])nc23)[N+]([O-])=O
InChI
1S/C12H8N4O6S.2Na.H2O/c13-23(21,22)8-3-1-2-5-9(8)7(16(19)20)4-6-10(5)15-12(18)11(17)14-6;;;/h1-4H,(H,14,17)(H,15,18)(H2,13,21,22);;;1H2/q;2*+1;/p-2
InChI 密鑰
LQSCHRKYVVVUFA-UHFFFAOYSA-L
基因資訊
human ... GRIA1(2890) , GRIA2(2891) , GRIA3(2892) , GRIA4(2893) , GRIK1(2897) , GRIK2(2898) , GRIK3(2899) , GRIK4(2900) , GRIK5(2901)
應用
NBQX 二钠盐水合物已被用于::
- 在 N -甲基- D -天冬氨酸受体 (NMDAR) 动力学研究中作为
- α-氨基-3-羟基-5-甲基-4-异恶唑丙酸 (AMPA) 受体拮抗剂,用于神经元细胞外液电流/电压 (I/V) 关系的电生理研究
- 及 NMDA 受体介导的兴奋性突触后电流 (EPSCs) 整流指数实验 (EPSC NMDAR )
生化/生理作用
NBQX 二钠盐水合物是一种具有神经保护作用的 AMPA/红藻氨酸谷氨酸受体拮抗剂。
特點和優勢
该化合物是受体分类及信号转导手册上谷氨酸受体(离子通道家族)页面上的特色化合物。想要浏览手册的其他页面, 请单击此处。
这种化合物是神经科学研究的特色产品。点击此处发现更多特色神经科学产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Predicting the functional states of human iPSC-derived neurons with single-cell RNA-seq and electrophysiology
Molecular Psychiatry, 21(11), 1573-1573 (2016)
Cross-modal reinstatement of thalamocortical plasticity accelerates ocular dominance plasticity in adult mice
Cell Reports, 24(13), 3433-3440 (2018)
The C-terminal tails of endogenous GluA1 and GluA2 differentially contribute to hippocampal synaptic plasticity and learning
Nature Neuroscience, 21(1), 50-50 (2018)
Neuron, 77(3), 542-558 (2013-02-12)
Membrane fusion during exocytosis is mediated by assemblies of SNARE (soluble NSF-attachment protein receptor) and SM (Sec1/Munc18-like) proteins. The SNARE/SM proteins involved in vesicle fusion during neurotransmitter release are well understood, whereas little is known about the protein machinery that
EMBO reports, 14(4), 389-394 (2013-02-16)
Propagation of tau pathology is linked with progressive neurodegeneration, but the mechanism underlying trans-synaptic spread of tau is unknown. We show that stimulation of neuronal activity, or AMPA receptor activation, induces tau release from healthy, mature cortical neurons. Notably, phosphorylation
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