Vonoprazan Fumarate是一种钾竞争性酸阻断剂 (P-CAB),对 H+/K+ ATPase 的抑制 IC50 为 17 nM,同时对 Na+/K+ ATPase 无影响,具有控制胃酸分泌的作用。
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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 HCl | ✔ | 95% | |||||||||||||||||
Gliquidone |
++
Potassium channel, IC50: 27.2 nM |
99% | |||||||||||||||||
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 HCl dihydrate | ✔ | 98% | |||||||||||||||||
ML133 HCl |
+
Kir2.1, IC50: 290 nM |
99% | |||||||||||||||||
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。 |
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]. |
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 |
CAS号 | 881681-01-2 |
分子式 | C21H20FN3O6S |
分子量 | 461.46 |
SMILES Code | O=S(N1C=C(CNC)C=C1C2=CC=CC=C2F)(C3=CC=CN=C3)=O.O=C(O)/C=C/C(O)=O |
MDL No. | MFCD18633280 |
别名 | TAK-438 |
运输 | 蓝冰 |
InChI Key | ROGSHYHKHPCCJW-WLHGVMLRSA-N |
Pubchem ID | 45375887 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place,Sealed in dry,2-8°C |
溶解方案 |
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 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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动物实验配方 |
0.5% methylcellulose+water 17 mg/mL suspension |