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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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V419367-50mg | 50mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $27.90 | |
V419367-100mg | 100mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $44.90 | |
V419367-250mg | 250mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $89.90 | |
V419367-1g | 1g | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $251.90 |
Synonyms | Vonoprazan (USAN/INN) | {[5-(2-fluorophenyl)-1-(pyridine-3-sulfonyl)-1H-pyrrol-3-yl]methyl}(methyl)amine | 1-[5-(2-fluorophenyl)-1-pyridin-3-ylsulfonyl-pyrrol-3-yl]-~{N}-methyl-methanamine | AC-36443 | TAK-438 free base | vonoprazanum | 4-hydroxy-4'-metho |
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Specifications & Purity | Moligand™, ≥98% |
Storage Temp | Protected from light,Store at -20°C,Argon charged |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of ATP4A |
Product Description |
Vonoprazan (TAK-438 free base), a proton pump inhibitor (PPI), is a potent potassium-competitive acid blocker (P-CAB), with antisecretory activity. Vonoprazan inhibits H+,K+-ATPase activity in porcine gastric microsomes with an IC50 of 19 nM at pH 6.5. Vonoprazan is developed for the research of acid-related diseases, such as gastroesophageal reflux disease and peptic ulcer disease. Vonoprazan can be used for eradication of Helicobacter pylori.
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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 1-[5-(2-fluorophenyl)-1-pyridin-3-ylsulfonylpyrrol-3-yl]-N-methylmethanamine |
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INCHI | InChI=1S/C17H16FN3O2S/c1-19-10-13-9-17(15-6-2-3-7-16(15)18)21(12-13)24(22,23)14-5-4-8-20-11-14/h2-9,11-12,19H,10H2,1H3 |
InChi Key | BFDBKMOZYNOTPK-UHFFFAOYSA-N |
Canonical SMILES | CNCC1=CN(C(=C1)C2=CC=CC=C2F)S(=O)(=O)C3=CN=CC=C3 |
Isomeric SMILES | CNCC1=CN(C(=C1)C2=CC=CC=C2F)S(=O)(=O)C3=CN=CC=C3 |
Alternate CAS | 881681-00-1 |
PubChem CID | 15981397 |
MeSH Entry Terms | 1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine;TAK 438;TAK-438;TAK438;Vonoprazan |
Molecular Weight | 345.39 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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F2404164 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404165 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404166 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404167 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404168 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404170 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404171 | Certificate of Analysis | Feb 28, 2024 | V419367 |
F2404172 | Certificate of Analysis | Feb 28, 2024 | V419367 |
Sensitivity | light & moisture & heat sensitive |
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1. Arikawa Y, Nishida H, Kurasawa O, Hasuoka A, Hirase K, Inatomi N, Hori Y, Matsukawa J, Imanishi A, Kondo M et al.. (2012) 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, 55 (9): (4446-56). [PMID:22512618] [10.1021/op500134e] |
2. Garnock-Jones KP. (2015) Vonoprazan: first global approval.. Drugs, 75 (4): (439-43). [PMID:25744862] [10.1021/op500134e] |
3. Otake K, Sakurai Y, Nishida H, Fukui H, Tagawa Y, Yamasaki H, Karashima M, Otsuka K, Inatomi N. (2016) Characteristics of the Novel Potassium-Competitive Acid Blocker Vonoprazan Fumarate (TAK-438).. Adv Ther, 33 (7): (1140-57). [PMID:27287852] [10.1021/op500134e] |
4. Scott DR, Munson KB, Marcus EA, Lambrecht NW, Sachs G. (2015) The binding selectivity of vonoprazan (TAK-438) to the gastric H+, K+ -ATPase.. Aliment Pharmacol Ther, 42 (11-12): (1315-26). [PMID:26423447] [10.1021/op500134e] |
5. Inatomi N, Matsukawa J, Sakurai Y, Otake K. (2016) Potassium-competitive acid blockers: Advanced therapeutic option for acid-related diseases.. Pharmacol Ther, 168 (13): (12-22). [PMID:27514776] [10.1021/op500134e] |
6. Abe K, Irie K, Nakanishi H, Suzuki H, Fujiyoshi Y. (2018) Crystal structures of the gastric proton pump.. Nature, 556 (7700): (214-218). [PMID:29618813] [10.1021/op500134e] |
7. Oshima T, Miwa H. (2018) Potent Potassium-competitive Acid Blockers: A New Era for the Treatment of Acid-related Diseases.. J Neurogastroenterol Motil, 24 (3): (334-344). [PMID:29739175] [10.1021/op500134e] |