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Oxotremorine M iodide

CAS No. 3854-04-4

Oxotremorine M iodide ( Oxotremorine methiodide )

产品货号. M26353 CAS No. 3854-04-4

Oxotremorine M iodide 是一种有效的非选择性毒蕈碱乙酰胆碱受体 (mAChR) 激动剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
10MG ¥348 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
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
    Oxotremorine M iodide
  • 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
    Oxotremorine M iodide 是一种有效的非选择性毒蕈碱乙酰胆碱受体 (mAChR) 激动剂。
  • 产品描述
    Oxotremorine M iodide is a potent and non-selective agonist of muscarinic acetylcholine receptor (mAChR).(In Vitro):Oxotremorine M iodide robustly elicits a phosphoinositide response (EC50 = 0.22 μM).?Oxotremorine M iodide shows EC50s of 0.36, 0.52, 1.62, and 1.48 μM for wild-type, M2, M3, and M2/M3 knockout mice, respectively.?Oxotremorine M iodide (0.1-30 μM) dose-dependently inhibits KCNQ2/3 currents.(In Vivo):In male Sprague-Dawley albino rats, Oxotremorine M iodide (0.5 mg/kg; s.c.) increases DA release in the medial prefrontal cortex without affecting the nucleus accumbens.
  • 体外实验
    Oxotremorine M iodide (0.1, 0.3, 1, 3, 10, 30 μM) inhibits KCNQ2/3 currents in the concentration-dependence. Oxotremorine M iodide elicits a robust phosphoinositide response characterized with an EC50 of 0.22 μM. Oxotremorine M iodide has EC50s of 0.36, 0.52, 1.62, and 1.48 μM for wild-type, M2, M3, and M2/M3 knockout mice, respectively.
  • 体内实验
    Oxotremorine M iodide (0.5 mg/kg; s.c.) increases Ddopamine (DA) release in the medial prefrontal cortex (mPFC) and has no effect in the nucleus accumbens (NAC) in male sprague-dawley albino rats weighing 250-350 g.
  • 同义词
    Oxotremorine methiodide
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    5-HT1| 5-HT2| 5-HT4
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    3854-04-4
  • 分子量
    322.19
  • 分子式
    C11H19IN2O
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 125 mg/mL (387.97 mM)
  • SMILES
    [I-].C[N+](C)(C)CC#CCN1CCCC1=O
  • 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.Marquez H, Albertí J, Salvà M, Saurina J, Sentellas S. Characterization of in vitro metabolic profiles of cinitapride obtained with liver microsomes of humans and various mammal species using UHPLC and chemometric methods for data analysis. Anal Bioanal Chem. 2012 May;403(4):909-16.
产品手册
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