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Submit ReviewBAY 1797 is a selective purinergic P2X4 receptor antagonist (IC50 values are 108, 112 and 233 nM for the human, mouse and rat P2X4, respectively). It is selective for P2X4 over P2X3, P2X7, and P2X1 receptors (IC50 values are 8.3, 10.6 and >50 μM, respectively, for the human receptors). BAY 1797 dose-dependently reduces prostaglandin E2 levels and exhibits anti-inflammatory and analgesic effects in an in vivo model of inflammatory pain. Orally active.
This probe is supplied in conjunction with the Structural Genomics Consortium. For further characterization details, please visit the BAY 1797 probe summary on the SGC website.
分子量 | 416.88 |
公式 | C20H17ClN2O4S |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 2055602-83-8 |
PubChem ID | 124125214 |
InChI Key | CSJYMAFXYMYNCK-UHFFFAOYSA-N |
Smiles | NS(=O)(C1=C(C=CC(NC(CC2=CC=CC=C2)=O)=C1)OC3=CC(Cl)=CC=C3)=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 | |||
DMSO | 41.69 | 100 | |
ethanol | 41.69 | 100 |
以下数据基于产品分子量 416.88。 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 | 2.4 mL | 11.99 mL | 23.99 mL |
5 mM | 0.48 mL | 2.4 mL | 4.8 mL |
10 mM | 0.24 mL | 1.2 mL | 2.4 mL |
50 mM | 0.05 mL | 0.24 mL | 0.48 mL |
参考文献是支持产品生物活性的出版物。
Werner et al (2019) Discovery and characterization of the potent and selective P2X4 inhibitor N-[4-(3-chlorophenoxy)-3-sulfamoylphenyl]-2-phenylacetamide (BAY-1797) and structure-guided amelioration of its CYP3A4 induction profile. J.Med.Chem. 62 11194 PMID: 31746599
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关键词: BAY 1797, BAY 1797 supplier, BAY1797, selective, antagonizes, antagonists, purinergic, P2X4, receptor, antinociceptive, anti-inflammatory, P2X, Receptors, 7573, Tocris Bioscience
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