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Submit ReviewSCH 28080 is a potent inhibitor of H+,K+-ATPase (IC50 = 20 nM); binds to the K+ recognition site and is competitive with respect to K+. Inhibits gastric acid secretion in vitro and in vivo.
分子量 | 277.33 |
公式 | C17H15N3O |
储存 | Store at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 76081-98-6 |
PubChem ID | 108137 |
InChI Key | PYKJFEPAUKAXNN-UHFFFAOYSA-N |
Smiles | CC1=C(CC#N)N2C=CC=C(OCC3=CC=CC=C3)C2=N1 |
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 | |||
ethanol | 2.77 | 10 | |
DMSO | 6.93 | 25 |
以下数据基于产品分子量 277.33。 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 |
---|---|---|---|
0.25 mM | 14.42 mL | 72.12 mL | 144.23 mL |
1.25 mM | 2.88 mL | 14.42 mL | 28.85 mL |
2.5 mM | 1.44 mL | 7.21 mL | 14.42 mL |
12.5 mM | 0.29 mL | 1.44 mL | 2.88 mL |
参考文献是支持产品生物活性的出版物。
Long et al (1983) Gastric antisecretory and cytoprotective activities of SCH 28080. J.Pharmacol.Exp.Ther. 226 114 PMID: 6864535
Scott et al (1987) Studies on the mechanism of action of the gastric microsomal (H+K+)-ATPase inhibitors SCH 32651 and SCH 28080. Biochem.Pharmacol. 36 97 PMID: 3026407
Vagin et al (2002) SCH 28080, a K+-competitive inhibitor of the gastric H,K-ATPase, binds near the M5-6 luminal loop, preventing K+ access to the ion binding domain. Biochemistry 41 12755 PMID: 12379118
If you know of a relevant reference for SCH 28080, please let us know.
关键词: SCH 28080, SCH 28080 supplier, H+K+-ATPase, inhibitors, inhibits, P-Type, ATPase, Ion, Transporters, Pumps, hydrogen, potassium-ATPase, SCH28080, H+,K+-ATPase, 1690, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 SCH 28080 的部分引用包括:
Lynch et al (2010) Heterogeneity of H-K-ATPase-mediated acid secretion along the mouse collecting duct. Am J Physiol Renal Physiol 298 F408 PMID: 19923411
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