Pumaprazole

Pumaprazole (BY-841) 是一种有效的、可逆的质子泵拮抗剂。

CAS号

158364-59-1

分子式

C19H22N4O2

主要靶点

Proton pump

仅限科研使用

Cat No : CM16712

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Synonyms

普马拉唑|BY-841



产品信息

Pumaprazole is an antagonist of a reversible proton pump.

CAS号 158364-59-1
分子式 C19H22N4O2
主要靶点 Proton pump
主要通路 离子通道
分子量 338.4
纯度 , 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 普马拉唑|BY-841

体内活性

Pumaprazole shows identical ID50 values on day 1 (11 μmol/kg, 95% confidence limits of 5 and 23), and on day 7 (10 μmol/kg, 95% confidence limits of 4 and 23) of a repeated dose study in this model. Basal acid secretion in the Ghosh-Schild rat is inhibited by Pumaprazole with a higher efficacy compared to ranitidine. The lower dose of Pumaprazole (27 μmol/kg) rapidly elevates luminal pH up to almost neutrality, the higher dose (54 μmol/kg) further prolongs this pH-elevating effect[1].

溶解度

DMSO:55 mg/ml (162.53 mM),Sonification is recommended.

参考文献

1.Kromer W, et al. Animal pharmacology of reversible antagonism of the gastric acid pump, compared to standard antisecretory principles. Pharmacology. 2000 May;60(4):179-87.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
×
=
×
C1   V1   C2   V2