Omeprazole Sodium
CAS No. 95510-70-6
Omeprazole Sodium ( H 16868 sodium )
产品货号. M27570 CAS No. 95510-70-6
奥美拉唑钠是一种质子泵抑制剂(PPI),可抑制胃酸分泌。奥美拉唑钠是一种有效的中性鞘磷脂酶 (N-SMase) 抑制剂(外泌体抑制剂)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 200MG | ¥113 | 有现货 |
|
| 500MG | ¥255 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥94 | 有现货 |
|
生物学信息
-
产品名称Omeprazole Sodium
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述奥美拉唑钠是一种质子泵抑制剂(PPI),可抑制胃酸分泌。奥美拉唑钠是一种有效的中性鞘磷脂酶 (N-SMase) 抑制剂(外泌体抑制剂)。
-
产品描述Omeprazole Sodium is a proton pump inhibitor(PPI) and suppresses gastric acid secretion. Omeprazole Sodium is a potent neutral sphingomyelinase (N-SMase) inhibitor (exosome inhibitor). Omeprazole Sodium shows competitive inhibition of CYP2C19 activity with a Ki of 2 to 6 μM. Omeprazole Sodium inhibits growth of Gram-positive and Gram-negative bacteria.(In Vivo):Omeprazole Sodium virtually eliminated intragastric acidity in all patients: the median 24 hour intragastric pH rose from 1.4 to 5.3 and the mean hourly hydrogen ion activity fell from 38.50 to 1.95 mmol(mEq)/1 (p less than 0.001) .
-
体外实验Omeprazole (H 16868) is a proton pump inhibitor used in the treatment of dyspepsia, peptic ulcer disease, gastroesophageal reflux disease, laryngopharyngeal reflux, and Zollinger-Ellison syndrome. Omeprazole (H 16868) virtually eliminated intragastric acidity in all patients: the median 24 hour intragastric pH rose from 1.4 to 5.3 and the mean hourly hydrogen ion activity fell from 38.50 to 1.95 mmol(mEq)/1 (p less than 0.001). This inhibition of 24 hour intragastric acidity is more profound than that previously reported with either cimetidine 1 g daily or ranitidine 300 mg daily. The pharmacokinetics of omeprazole were studied in a group of healthy male subjects after single and repeated oral doses of 30 and 60 mg. Absorption of Omeprazole (H 16868) from its enteric-coated formulation was unpredictable. There was a highly significant increase in the area under the plasma concentration time curve (AUC) after repeated dosing. Omeprazole (H 16868) increases its own relative availability following repeated dosing. This may be due to inhibition of gastric acid secretion by omeprazole which is an acid-labile compound.Omeprazole sodium is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor (exosome inhibitor).
-
体内实验——
-
同义词H 16868 sodium
-
通路Metabolic Enzyme/Protease
-
靶点P450
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number95510-70-6
-
分子量367.4
-
分子式C17H18N3NaO3S
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 125 mg/mL (340.23 mM)
-
SMILESCOC1=CC2=C(C=C1)[N]([Na])C(=N2)[S](=O)CC3=NC=C(C)C(=C3C)OC
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Masanori Miwa, et al. Food Applications of Curdlan. Food Hydrocolloids pp 119-124.
产品手册
关联产品
-
Chamaechromone
Chamaechromone 是从 Stellera chamaejasme L. 的根中分离出来的天然产物。 Chamaechromone 具有抗 HBV 和杀虫活性。
-
Verapamil
Verapamil 是一种钙通道阻滞剂,也是一种口服有效的 P-gp 抑制剂。
-
AS1810722
AS1810722 是一种口服有效的 STAT6 抑制剂 (IC50 :1.9 nM)。 AS1810722 显示出良好的 CYP3A4 抑制特性。 AS1810722是稠合双环嘧啶的衍生物,具有用于哮喘等过敏性疾病和特应性疾病研究的潜力。
021-51111890
购物车()
sales@molnova.cn

