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Famotidine

CAS No. 76824-35-6

Famotidine ( MK-208 | YM-11170 )

产品货号. M15908 CAS No. 76824-35-6

法莫替丁是一种竞争性组胺 H2 受体拮抗剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Famotidine
  • 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
    法莫替丁是一种竞争性组胺 H2 受体拮抗剂。
  • 产品描述
    Famotidine is a competitive histamine H2-receptor antagonist. Its main pharmacodynamic effect is the inhibition of gastric secretion.(In Vitro):Famotidine (MK-208) is a histamine H2-receptor antagonist that inhibits stomach acid production, and it is commonly used in the treatment of peptic ulcer disease (PUD) and gastroesophageal reflux disease (GERD/GORD). Famotidine (MK-208) Group(2 mg/kg/day) were significantly lower than the equivalent parameters for the Control Group on both the third and seventh days post-surgery. Famotidine (MK-208) exerts detrimental effects on the anastomotic bursting pressure and hydroxyproline content of perianastomotic tissues in the colon of rats. Famotidine (MK-208) increased the transgastric potential difference (PD) and promoted the recovery of decreased transgastric PD induced by acidified ethanol in rats. The preventive effect of famotidine on gastric lesions is attributable not only to suppression of acid secretion but to activation of the gastric mucosal defensive mechanisms.
  • 体外实验
    Famotidine (MK-208) is a histamine H2-receptor antagonist that inhibits stomach acid production, and it is commonly used in the treatment of peptic ulcer disease (PUD) and gastroesophageal reflux disease (GERD/GORD). Famotidine (MK-208) Group(2 mg/kg/day) were significantly lower than the equivalent parameters for the Control Group on both the third and seventh days post-surgery. Famotidine (MK-208) exerts detrimental effects on the anastomotic bursting pressure and hydroxyproline content of perianastomotic tissues in the colon of rats. Famotidine (MK-208) increased the transgastric potential difference (PD) and promoted the recovery of decreased transgastric PD induced by acidified ethanol in rats. The preventive effect of famotidine on gastric lesions is attributable not only to suppression of acid secretion but to activation of the gastric mucosal defensive mechanisms.
  • 体内实验
    ——
  • 同义词
    MK-208 | YM-11170
  • 通路
    GPCR/G Protein
  • 靶点
    Histamine Receptor
  • 受体
    H2 receptor
  • 研究领域
    Other Indications
  • 适应症
    ——

化学信息

  • CAS Number
    76824-35-6
  • 分子量
    337.45
  • 分子式
    C8H15N7O2S3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: 67 mg/mL (198.54 mM)
  • SMILES
    N/C(N)=N\C1=NC(CSCC/C(N)=N/S(=O)(N)=O)=CS1
  • 化学全称
    (Z)-3-(((2-((diaminomethylene)amino)thiazol-4-yl)methyl)thio)-N'-sulfamoylpropanimidamide

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. Takahashi HK, et al. Mol Pharmacol. 2006 Aug;70(2):450-3.
产品手册
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