الصفحة الرئيسية>>Signaling Pathways>> Membrane Transporter/Ion Channel>> Proton Pump>>Vonoprazan

Vonoprazan

رقم الكتالوجGC37920

Vonoprazan (قاعدة خالية من TAK-438) ، مثبط مضخة البروتون (PPI) ، هو مانع حمض قوي وفعال عن طريق الفم منافس للبوتاسيوم (P-CAB) ، مع نشاط مضاد للإفراز

Products are for research use only. Not for human use. We do not sell to patients.

Vonoprazan التركيب الكيميائي

Cas No.: 881681-00-1

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
27٫00
متوفر
50mg
25٫00
متوفر
100mg
35٫00
متوفر
250mg
70٫00
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com

مراجعات العميل

بناء على آراء العملاء.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

    Bioactive Compounds Premium Provider

Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Vonoprazan (TAK-438 free base) is an orally active potassium-competitive acid blocker which inhibits H+, K+-ATPase activity with an IC50 of 19 nM.

[1]. Arikawa Y, 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, 55(9), 4446-4456. [2]. Hori Y, 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, 335(1), 231-238. [3]. Hori Y, et al. A study comparing the antisecretory effect of TAK-438, a novel potassium-competitive acid blocker, with lansoprazole in animals. J Pharmacol Exp Ther, 2011, 337(3), 797-804.

مراجعات

Review for Vonoprazan

Average Rating: 5 ★★★★★ (Based on Reviews and 32 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for Vonoprazan

GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.

Required fields are marked with *

You may receive emails regarding this submission. Any emails will include the ability to opt-out of future communications.