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T1756LIlaprazole艾普拉唑；IY81149；IY-81149；IY 81149
Ilaprazole is a proton pump inhibitor used in the treatment of dyspepsia gastroesophageal reflux disease (GORD/GERD) and duodenal ulcer. Studies also showed that Ilaprazole significantly prevented the development of reflux oesophagitis.
价 格：￥电议型 号：T1756L产 地：中国大陆
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T1756Ilaprazole sodium艾普拉唑钠；IY-81149 sodium
Ilaprazole, a substituted benzimidazole prodrug, is a selective and irreversible proton pump inhibitor. A weak base, Ilaprazole accumulates in the acidic environment of the secretory canaliculus of the gastric parietal cell where it is converted to an act
价 格：￥电议型 号：T1756产 地：中国大陆
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T1756Ilaprazole sodiumIlaprazole sodium,IY-81149 sodium,
Ilaprazole, a substituted benzimidazole prodrug, is a selective and irreversible proton pump inhibitor. A weak base, Ilaprazole accumulates in the acidic environment of the secretory canaliculus of the gastric parietal cell where it is converted to an act
价 格：￥电议型 号：T1756产 地：美洲
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T78218Ilaprazole sodium hydrate；化合物 Ilaprazole sodium hydrateIY-81149 sodium hydrate；IY-81149 sodium hydra
Ilaprazole (IY-81149) sodium hydrate is an orally active proton pump inhibitor that irreversibly inhibits H+/K+-ATPase in rabbit parietal cells with a dose-dependent IC50 of 6 μM. It is employed in gastric ulcer research and acts as a potent inhibitor of T-lymphokine-activated killer cell-originated protein kinase (TOPK) [1] [2].
价 格：￥电议型 号：T78218产 地：中国大陆
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T1756LIlaprazole；艾普拉唑IY81149|||IY 81149|||IY-81149；IY81149|||艾普拉唑|||IY 81149|||IY-81149
Ilaprazole (IY-81149) is a proton pump inhibitor used in the treatment of dyspepsia gastroesophageal reflux disease (GORD/GERD) and duodenal ulcer. Studies also showed that Ilaprazole significantly prevented the development of reflux oesophagitis.
价 格：￥电议型 号：T1756L产 地：中国大陆
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T1756Ilaprazole sodium；艾普拉唑钠IY-81149 sodium；IY-81149 sodium|||艾普拉唑钠
Ilaprazole sodium (IY-81149 sodium) , a substituted benzimidazole prodrug, is a selective and irreversible proton pump inhibitor. A weak base, Ilaprazole accumulates in the acidic environment of the secretory canaliculus of the gastric parietal cell where it is converted to an active sulfenamide form that binds to cysteine sulfhydryl groups on the luminal aspect of the proton pump hydrogen-potassium adenosine triphosphatase (H+/K+ ATPase), thereby inhibiting the pump´s activity and the par
价 格：￥电议型 号：T1756产 地：中国大陆
