Vonoprazan - 98%, high purity , CAS No.881681-00-1, Inhibitor of ATP4A

Item Number
V419367
Grouped product items
SKUSizeAvailabilityPrice Qty
V419367-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$27.90
V419367-100mg
100mg
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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

Basic Description

SynonymsVonoprazan (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
Specifications & PurityMoligand™, ≥98%
Storage TempProtected from light,Store at -20°C,Argon charged
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor 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.

Associated Targets(Human)

ATP4A Tclin Potassium-transporting ATPase alpha chain 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 1-[5-(2-fluorophenyl)-1-pyridin-3-ylsulfonylpyrrol-3-yl]-N-methylmethanamine
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

Certificates

Certificate of Analysis(COA)

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8 results found

Lot NumberCertificate TypeDateItem
F2404164Certificate of AnalysisFeb 28, 2024 V419367
F2404165Certificate of AnalysisFeb 28, 2024 V419367
F2404166Certificate of AnalysisFeb 28, 2024 V419367
F2404167Certificate of AnalysisFeb 28, 2024 V419367
F2404168Certificate of AnalysisFeb 28, 2024 V419367
F2404170Certificate of AnalysisFeb 28, 2024 V419367
F2404171Certificate of AnalysisFeb 28, 2024 V419367
F2404172Certificate of AnalysisFeb 28, 2024 V419367

Chemical and Physical Properties

Sensitivitylight & moisture & heat sensitive

Related Documents

References

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]

Solution Calculators