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富马酸沃诺拉赞 /Vonoprazan Fumarate {[allProObj[0].p_purity_real_show]}

货号:A108580 同义名: TAK-438

TAK-438, a potassium proton pump inhibitor, can reversibly inhibit H+/K+ ATPase with IC50 of 17 nM and does not affect Na+/K+ ATPase. It also controls gastric acid secretion.

Vonoprazan Fumarate 化学结构 CAS号:881681-01-2
Vonoprazan Fumarate 化学结构
CAS号:881681-01-2
Vonoprazan Fumarate 3D分子结构
CAS号:881681-01-2
Vonoprazan Fumarate 化学结构 CAS号:881681-01-2
Vonoprazan Fumarate 3D分子结构 CAS号:881681-01-2
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Vonoprazan Fumarate 纯度/质量文件 产品仅供科研

货号:A108580 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Potassium Channel 其他靶点 纯度
Tolbutamide 98%
Glimepiride ++++

SUR1, IC50: 5.4 nM

SUR2B, IC50: 7.3 nM

97%
Dronedarone Hydrochloride 95%
Gliquidone ++

Potassium channel, IC50: 27.2 nM

98%
TRAM-34 +++

IKCa1 (KCa3.1), Kd: 20 nM

98%
Glibenclamide 98%
Amiodarone HCl 97%
Gliclazide ++

Potassium channel, IC50: 184 nM

98%
Repaglinide 98%
Dofetilide 98%
Nateglinide 99%
Quinine hydrochloride dihydrate 98%
ML133 HCl +

Kir2.1, IC50: 290 nM

97%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Vonoprazan Fumarate 生物活性

描述 The potassium-competitive acid blocker (P-CAB), a new class of acid suppressant, inhibits gastric H+,K+-ATPase activity by reversible and K+-competitive ionic binding to the enzyme. TAK-438 is a novel P-CAB that reversibly inhibits H+,K+-ATPase with IC50 of 19 nM (pH 6.5), and exhibits potent gastric acid secretion inhibitory action in vivo. And TAK-438 was selected as a drug candidate for the treatment of gastroesophageal reflux disease (GERD), peptic ulcer, and other acid-related diseases [3]. Under weakly acidic conditions (pH 6.5), TAK-438 inhibited gastric H+,K+-ATPase activity in a concentration-dependent manner. Under neutral conditions (pH 7.5), the inhibitory activity of TAK-438 was almost the same as that under weakly acidic conditions. In Pylorus-Ligated rats, TAK-438 at doses of 0.5, 1, 2, and 4 mg/kg inhibited basal gastric acid secretion in a dose-dependent manner, and the ID50 value was 1.26 mg/kg. In Anesthetized rats, TAK-438 inhibited 2DG-stimulated gastric acid secretion in a dose-dependent manner, and the ID50 value of TAK-438 was 0.83 mg/kg. TAK-438 completely inhibited gastric acid secretion at the 4 mg/kg dose [4].
作用机制 TAK-438 inhibited gastric H+,K+-ATPase in a K+-competitive manner [4].

Vonoprazan Fumarate 参考文献

[1]Arikawa Y, Nishida H, et al. Discovery of a novel pyrrole derivative 1-[5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl] -N-methylmethanamine fumarate (TAK-438) as a potassium-competitive acid blocker (P-CAB). J Med Chem. 2012 May 10;55(9):4446-56.

[2]Hori Y, Imanishi A, et al. 1-[5-(2-Fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl] -N-methylmethanamine monofumarate (TAK-438), a novel and potent potassium-competitive acid blocker for the treatment of acid-related diseases. J Pharmacol Exp Ther. 2010 Oct;335(1):231-8.

[3]Arikawa Y, Nishida H, Kurasawa O, Hasuoka A, Hirase K, Inatomi N, Hori Y, Matsukawa J, Imanishi A, Kondo M, Tarui N, Hamada T, Takagi T, Takeuchi T, Kajino M. Discovery of a novel pyrrole derivative 1-[5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamine fumarate (TAK-438) as a potassium-competitive acid blocker (P-CAB). J Med Chem. 2012 May 10;55(9):4446-56. doi: 10.1021/jm300318t. Epub 2012 Apr 30. PMID: 22512618.

[4]Hori Y, Imanishi A, Matsukawa J, Tsukimi Y, Nishida H, Arikawa Y, Hirase K, Kajino M, Inatomi N. 1-[5-(2-Fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamine monofumarate (TAK-438), a novel and potent potassium-competitive acid blocker for the treatment of acid-related diseases. J Pharmacol Exp Ther. 2010 Oct;335(1):231-8. doi: 10.1124/jpet.110.170274. Epub 2010 Jul 12. Erratum in: J Pharmacol Exp Ther. 2016 Jul;358(1):1-2. PMID: 20624992.

Vonoprazan Fumarate 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.17mL

0.43mL

0.22mL

10.84mL

2.17mL

1.08mL

21.67mL

4.33mL

2.17mL

Vonoprazan Fumarate 技术信息

CAS号881681-01-2
分子式C21H20FN3O6S
分子量 461.463
别名 TAK-438
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,Room temperature

溶解度

DMSO: 50 mg/mL(108.35 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方

0.5% methylcellulose+water 17 mg/mL suspension

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