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Lansoprazole CAS NO.103577-45-3

Min.Order Quantity:
10 Gram
Purity:
99%
Port:
Tianjin xingang
Payment Terms:
T/T,Western Union,MoneyGram,Other

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Product Details

Keywords

  • Lansoprazole
  • 103577-45-3,chemical
  • research,C16H14F3N3O2S

Quick Details

  • ProName: Lansoprazole
  • CasNo: 103577-45-3
  • Molecular Formula: C16H14F3N3O2S
  • Appearance: Solid
  • Application: Orally active estrogenic steroid. It w...
  • DeliveryTime: 3days
  • PackAge: in foil bag or customized
  • Port: Tianjin xingang
  • ProductionCapacity: 10 Kilogram/Week
  • Purity: 99%
  • Storage: Refrigerator
  • Transportation: shipping by courier or by sea
  • LimitNum: 10 Gram

Superiority

product name: lansoprazole
synonyms: 1h-benzimidazole,2-(((3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl)methyl)su;2-(((3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl)methyl)sulfinyl)-1h-benz;lfinyl)-;prevacid;ogast;lansoprazole;lansaprazole;lansox
cas: 103577-45-3
mf: c16h14f3n3o2s
mw: 369.36
einecs:
product categories: active pharmaceutical ingredients;intermediates & fine chemicals;pharmaceuticals;sulfur & selenium compounds;ion pump inhibitors;monovalent ion channels;voltage-gated ion channels;atpase;pharmaceutical intermediates;api reference standardfree base api;other apis;pharmaceutical

Details

lansoprazole usage and synthesis
chemical properties white crystalline powder
usage used as a gastric proton pump inhibitor. an antiulcerative
usage anthelmintic
usage a h+,k+-atpase inhibitor that displays antisecretory activity
usage treatment of gastroesophageal reflux disease (gerd), erosive esophagitis, duodenal ulcers, helicobacter pylori (h. pylori) infections,stomach ulcers, prevention of stomach ulcers in those people taking non-steroidal anti-inflammatory drugs (nsaids), such
usage for the treatment of acid-reflux disorders (gerd), peptic ulcer disease, h. pylori eradication, and prevention of gastroinetestinal bleeds with nsaid use.
biological activity h + ,k + -atpase inhibitor (ic 50 = 6.3 μ m) that displays antisecretory and antiulcer activity. inhibits gastric acid secretion (ic 50 = 0.09 μ m for histamine-induced acid formation) and reduces gastric lesion formation induced by a variety of ulcerative stimuli. antibacterial against helicobacter pylori in vitro . also blocks swelling-dependent chloride channel (iciswell) in nih3t3 fibroblasts. more potent than omeprazole (5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1h-benzimidazole ).

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