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Submit Review5,7-Dichlorokynurenic acid sodium salt is a sodium salt of 5,7-Dichlorokynurenic acid (Cat. No. 0286), a potent antagonist at the glycine site of the NMDA receptor (Ki = 79 nM vs. [3H]-glycine).
分子量 | 280.04 |
公式 | C10H4Cl2NNaO3 |
储存 | Desiccate at RT |
纯度 | ≥98% (HPLC) |
CAS Number | 1184986-70-6 |
PubChem ID | 44134672 |
InChI Key | VPRPMJHKWHCUFW-UHFFFAOYSA-M |
Smiles | [Na+].OC1=CC(=NC2=CC(Cl)=CC(Cl)=C12)C([O-])=O |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
1eq. NaOH | 28 | 100 |
以下数据基于产品分子量 280.04。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.57 mL | 17.85 mL | 35.71 mL |
5 mM | 0.71 mL | 3.57 mL | 7.14 mL |
10 mM | 0.36 mL | 1.79 mL | 3.57 mL |
50 mM | 0.07 mL | 0.36 mL | 0.71 mL |
参考文献是支持产品生物活性的出版物。
Baron et al (1990) Activity of 5,7-dichlorokynurenic acid. A potent antagonist at the NMDA receptor-associated glycine binding site. Mol.Pharmacol. 38 554 PMID: 2172769
Moore et al (1990) Substituted kynurenic acid derivatives. Potent and selective antagonists at the glycine site on the NMDA receptor. Eur.Fed.Med.Chem. (under auspices of IUPAC) XIth I
If you know of a relevant reference for 5,7-Dichlorokynurenic acid sodium salt, please let us know.
关键词: 5,7-Dichlorokynurenic acid sodium salt, 5,7-Dichlorokynurenic acid sodium salt supplier, Potent, NMDA, antagonists, glycine, site, Glutamate, Receptors, N-Methyl-D-Aspartate, iGluR, Ionotropic, 3698, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 5,7-Dichlorokynurenic acid sodium salt 的部分引用包括:
Rafael et al (2022) GluN3A excitatory glycine receptors control adult cortical and amygdalar circuits. Neuron 110 2438-2454.e8 PMID: 35700736
Lan-Zhen et al (2019) Differences in the Conformational Energy Landscape of CDK1 and CDK2 Suggest a Mechanism for Achieving Selective CDK Inhibition. Cell Chem Biol 26 121-130.e5 PMID: 30472117
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