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117976-89-3

117976-89-3 structure
117976-89-3 structure
  • Name: Rabeprazole
  • Chemical Name: rabeprazole
  • CAS Number: 117976-89-3
  • Molecular Formula: C18H21N3O3S
  • Molecular Weight: 359.443
  • Catalog: API Digestive system medication Acid and gastric mucosal protective drugs
  • Create Date: 2018-05-16 08:00:00
  • Modify Date: 2024-01-02 18:41:45
  • Rabeprazole is an antiulcer drug in the class of proton pump inhibitors.Target: Proton PumpRabeprazole belongs to a class of antisecretory compounds (substituted benzimidazole proton-pump inhibitors) that do not exhibit anticholinergic or histamine H2-receptor antagonist properties, but suppress gastric acid secretion by inhibiting the gastric H+/K+ATPase (hydrogen-potassium adenosine triphosphatase) at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton-pump inhibitor. Rabeprazole blocks the final step of gastric acid secretion. In gastric parietal cells, rabeprazole is protonated, accumulates, and is transformed to an active sulfenamide. When studied in vitro, rabeprazole is chemically activated at pH 1.2 with a half-life of 78 seconds.

Name rabeprazole
Synonyms Rebeprazole
2-[[[4-(3-Methoxypropoxy)-3-methyl-2-pyridinyl]methyl]sulfinyl]-1H-benzimidazole
Pariprazole
2-(((4-(3-methoxypropoxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1H-benzo[d]imidazole
2-({[4-(3-Methoxypropoxy)-3-methyl-2-pyridinyl]methyl}sulfinyl)-1H-benzimidazole
MFCD00868879
Rabeprazole
1H-Benzimidazole, 2-[[[4-(3-methoxypropoxy)-3-methyl-2-pyridinyl]methyl]sulfinyl]-
2-({[4-(3-Methoxypropoxy)-3-methylpyridin-2-yl]methyl}sulfinyl)-1H-benzimidazole
Description Rabeprazole is an antiulcer drug in the class of proton pump inhibitors.Target: Proton PumpRabeprazole belongs to a class of antisecretory compounds (substituted benzimidazole proton-pump inhibitors) that do not exhibit anticholinergic or histamine H2-receptor antagonist properties, but suppress gastric acid secretion by inhibiting the gastric H+/K+ATPase (hydrogen-potassium adenosine triphosphatase) at the secretory surface of the gastric parietal cell. Because this enzyme is regarded as the acid (proton) pump within the parietal cell, rabeprazole has been characterized as a gastric proton-pump inhibitor. Rabeprazole blocks the final step of gastric acid secretion. In gastric parietal cells, rabeprazole is protonated, accumulates, and is transformed to an active sulfenamide. When studied in vitro, rabeprazole is chemically activated at pH 1.2 with a half-life of 78 seconds.
Related Catalog
References

[1]. http://www.drugbank.ca/drugs/DB01129

Density 1.3±0.1 g/cm3
Boiling Point 603.9±65.0 °C at 760 mmHg
Melting Point 202-204°C
Molecular Formula C18H21N3O3S
Molecular Weight 359.443
Flash Point 319.1±34.3 °C
Exact Mass 359.130371
PSA 96.31000
LogP 1.83
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.655
Storage condition -20℃
Hazard Codes Xi
Risk Phrases R36/38
Safety Phrases S26-S36

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Literature: US2009/5570 A1, ; Page/Page column 3-4 ;

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Literature: EP1992619 A1, ; Page/Page column 16 ;

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Literature: US2007/249662 A1, ; Page/Page column 5 ;

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Literature: US5948789 A1, ; US 5948789 A

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Literature: US5948789 A1, ; US 5948789 A

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Literature: EP1921075 A2, ; Page/Page column 8 ;

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Literature: WO2006/24890 A1, ; Page/Page column 6-7 ;

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Literature: EP1818331 A1, ; Page/Page column 6 ;