Indications and Uses Mechanisms of Action Clinical Research Patents
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Vonoprazan

Indications and Uses Mechanisms of Action Clinical Research Patents
Product Name
Vonoprazan
CAS No.
881681-00-1
Chemical Name
Vonoprazan
Synonyms
1-[5-(2-Fluorophenyl)-1-[(pyridin-3-yl)sulfonyl]-1H-pyrrol-3-yl]-N-methylmethanamine;Vonoprazan;Vonoprazan-025;TAK-438 (free base);Vonoprazan USP/EP/BP;TAK438 Intermediate 6;Vonoprazan Impurity 132;Vonoprazan Impurity 133;Vonoprazan Impurity 134;Vonoprazan Impurity 135
CBNumber
CB22716734
Molecular Formula
C17H16FN3O2S
Formula Weight
345.39
MOL File
881681-00-1.mol
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Vonoprazan Property

Boiling point:
530.3±60.0 °C(Predicted)
Density 
1.31±0.1 g/cm3(Predicted)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka
9.06±0.10(Predicted)
form 
Solid
color 
Pale Yellow to Light Yellow
Stability:
Hygroscopic
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
InChIKey
BFDBKMOZYNOTPK-UHFFFAOYSA-N
SMILES
N1(S(C2=CC=CN=C2)(=O)=O)C(C2=CC=CC=C2F)=CC(CNC)=C1
CAS DataBase Reference
881681-00-1
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
V767015
Product name
Vonoprazan
Packaging
50mg
Price
$50
Updated
2021/12/16
TRC
Product number
V767015
Product name
Vonoprazan
Packaging
500mg
Price
$160
Updated
2021/12/16
ChemScene
Product number
CS-5555
Product name
Vonoprazan
Purity
99.89%
Packaging
100mg
Price
$50
Updated
2021/12/16
ChemScene
Product number
CS-5555
Product name
Vonoprazan
Purity
99.89%
Packaging
250mg
Price
$100
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0026066
Product name
TAK-438
Purity
95.00%
Packaging
5MG
Price
$503.91
Updated
2021/12/16
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Vonoprazan Chemical Properties,Usage,Production

Indications and Uses

  Vanoprazan fumarate is a new oral gastric acidity drug developed by Takeda Pharmaceutical and Otsuka Pharmaceuticals. It is used to treat duodenal ulcers, gastric ulcers, reflux esophagitis, gastric ulcers or recurrent duodenal ulcers caused by low dosages of Aspirin, and Helicobacter pylori. It can also supplement treatment of gastric ulcers, duodenal ulcers, gastric MALT lymphoma, idiopathic thrombocytopenic purpura, early gastric cancer, and Helicobacter pylori infection gastritis.
Compared to traditional irreversible proton pump inhibitors (omeprazole, esomeprazole, etc.), Takecab has the following advantages:
1. Rapid effects, having the most drastic acid-suppressing effects on the first day of ingestion.
2. Oral intake, efficacy unaffected by gastric acid, does not require enteric administration.
Alleviated nighttime acid reflux.

Mechanisms of Action

Takecab (TAK-438) is a kind of potassium ion (K+) competitive acid blocker (P-CAB) and a reversible proton pump inhibitor. After this product enters the body, at the last step of gastric parietal cell acid secretion, it inhibits K+ ions from bonding with H+-K+-ATP enzymes (proton pump), thus stopping gastric acid secretion. It has a strong, lasting gastric acid suppression effect. TAK-438 is not mainly metabolized by protein CYP2C19, and it does not need to be activated by acid to inhibit protein pumps. As the drug enters the stomach at a high concentration, it will have the strongest suppressing effect at its first dosage, an effect which can last for up to 24 hours. TAK-438 is a stable acid, its formula is readily available and does not require optimized formulation (e.g. enteric coating), and its effective dosage amount does not vary dramatically between different patients.

Clinical Research

Compared to the traditional protein pump inhibitor Lansoprazole, Vonoprazan takes effect through competitive and reversible inhibition of K+ in protein pumps. Clinical and animal experiments show that Vonoprazan acts faster than PPI or H2 receptor blockers, has a stronger pH raising effect, can swiftly alleviate gastric symptoms, allows enzyme recovery after dissociation, and has few side effects. Multiple clinical trials have proved that in cases of erosive esophagitis, Vonoprazan prevents and treats gastric and duodenal ulcers. As a first-line response for eradicating helicobacter pylori, it has shown significant efficacy, higher than Lansoprazole and with minimal side effects.
Vonoprazan has high lipophilicity and dissociation constant, so in acidic environments, it can take effect without the activation of acid. Vonoprazan’s inhibition of protein pumps does not require acid activation. Upon entering the stomach at a high concentration in its first dosage, it produces its strongest inhibiting effect, which can last for 24 hours. Vonoprazan is a stable acid, and it can rapidly increase the pH in the stomach and suppress gastric acid.
Vonoprazan has minimal influence on other enzyme and bodily functions, making it very safe and tolerable. Traditional PPIs are metabolized by CYP2C19, while Vonoprazan is not. Its efficacy and required dosage do not differ dramatically in different patients, making it an advantageous individualized drug regimen for patients.

Patents

Chemical compound patent: 200680040789.7, application date: August 29, 2006, expiration date: August 29, 2026, legal status: holding rights.
Process patent: 201080018114.9, application date: February 24, 2013, expiration date: February 24, 2030. Legal status: In review – trial.
Composition patent: WO2014003199, application date: June 26, 2013, no Chinese patent.

Uses

Vonoprazan is used to treat an infection caused by the bacteria H. pylori. This bacteria can cause stomach/intestinal ulcers and irritation/swelling of the lining of the stomach. It may also increase the risk of stomach cancer. Treating the infection will help the ulcers get better and reduces the risk of serious damage to the lining of the stomach/intestines (such as bleeding, tearing).Vonoprazan is an acid blocker. It works by blocking acid production in the stomach. Decreasing excess stomach acid can help ulcers heal. Amoxicillin is an antibiotic used to treat a wide variety of bacterial infections (including H. pylori). Treating the infection helps the ulcers heal and reduces the risk of ulcers returning. Amoxicillin is a penicillin-type antibiotic. It works by stopping the growth of bacteria. Amoxicillin treats only bacterial infections. It will not work for viral infections (such as common cold, flu).

Definition

ChEBI: Vonoprazan is a member of pyrroles.

Side effects

Vonoprazan may cause any of the following side effects: diarrhoea, constipation, nausea, stomach discomfort, bloatedness, changes in taste, and rash. Some side effects may need immediate medical help.

Vonoprazan Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Vonoprazan manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Vonoprazan 881681-00-1
Price
US $0.00-0.00/Kg/Drum
Min. Order
1KG
Purity
99%min
Supply Ability
100kg
Release date
2021-10-22
BEIJING SJAR TECHNOLOGY DEVELOPMENT CO., LTD.
Product
Vonoprazan 881681-00-1
Price
US $0.00/g
Min. Order
1g
Purity
More Than 99%
Supply Ability
100kg/Month
Release date
2024-11-15
Shaanxi Dideu Medichem Co. Ltd
Product
Vonoprazan 881681-00-1
Price
US $1.00-1.00/Kg/Bag
Min. Order
1g
Purity
99%
Supply Ability
50tons
Release date
2020-04-30

881681-00-1, VonoprazanRelated Search:


  • Vonoprazan
  • 1-[5-(2-Fluorophenyl)-1-[(pyridin-3-yl)sulfonyl]-1H-pyrrol-3-yl]-N-methylmethanamine
  • 1H-Pyrrole-3-methanamine,5-(2-fluorophenyl)-N-methyl-1-(3-pyridinylsulfonyl)
  • TAK-438 (free base)
  • Vonoprazan-025
  • Voronazan interfluoroisomer
  • Vonoprazan related Impuirty 29
  • Vonoprazan m-Fluoro Isomer
  • Vonopraza/Vonoprazan fumarate
  • Vonoprazan USP/EP/BP
  • Vonoprazan Impurity 132
  • Vonoprazan Impurity 133
  • Vonoprazan Impurity 134
  • Vonoprazan Impurity 135
  • TAK438 Intermediate 6
  • 1- [5- (2-Fluorophenyl)-1- (pyridine-3-sulfonyl)-1H-pyrrol-3-yl] N-methylmethanamine
  • Vonoprazan Impurity 186
  • 881681-00-1
  • API