• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

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
100MG ¥332 有现货
200MG ¥470 有现货
500MG ¥786 有现货
1G 获取报价 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 Number
    95510-70-6
  • 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)
  • SMILES
    COC1=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
  • N-Nornuciferine hydr...

    N-Nornuciferine 是荷叶中的一种阿朴啡生物碱,显着抑制 CYP2D6(IC50:3.76 μM,Ki:2.34 μM)。N-Nornuciferine 强烈抑制 CYP2D6 活性,但对其他四种 P450 同工酶(CYP2C19、CYP3A4、 CYP2E1、CYP2C9)。 N-Nornuciferine 竞争性抑制 CYP2D6 催化的右美沙芬 O-去甲基化 (Ki: 2.34 μM)。

  • EN3356

    EN3356 is an orally available and selective inhibitor of steroidal 17-alpha-hydroxylase/C17,20 cleavage enzyme (CYP17A1 or CYP17), a non-steroidal cleavage enzyme-selective compound with potential anti-androgenic and anti-tumor activity.

  • Abiraterone

    Abiraterone (CB-7598) 是一种有效的类固醇细胞色素 P450 17α-羟化酶-17,20-裂合酶 (CYP17) 抑制剂,IC50 为 4 nM。