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Oxotremorine M iodide

CAS No. 3854-04-4

Oxotremorine M iodide( Oxotremorine methiodide )

Catalog No. M26353 CAS No. 3854-04-4

Oxotremorine M iodide is a potent and non-selective agonist of muscarinic acetylcholine receptor (mAChR).

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    Oxotremorine M iodide
  • Note
    Research use only, not for human use.
  • Brief Description
    Oxotremorine M iodide is a potent and non-selective agonist of muscarinic acetylcholine receptor (mAChR).
  • Description
    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.
  • In Vitro
    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.
  • In Vivo
    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.
  • Synonyms
    Oxotremorine methiodide
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    5-HT1| 5-HT2| 5-HT4
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    3854-04-4
  • Formula Weight
    322.19
  • Molecular Formula
    C11H19IN2O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (387.97 mM)
  • SMILES
    [I-].C[N+](C)(C)CC#CCN1CCCC1=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

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.
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