Oxybutynin

CAS No. 5633-20-5

Oxybutynin( —— )

Catalog No. M15049 CAS No. 5633-20-5

Oxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Oxybutynin
  • Note
    Research use only, not for human use.
  • Brief Description
    Oxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties.
  • Description
    Oxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties.(In Vitro):Oxybutynin (0.1, 0.3, 1, 3, 10, 30, 100 μM; 200 ms) inhibits vascular Kv channels in a concentration-dependent manner independent of anticholinergic effect in coronary arterial smooth muscle cells.(In Vivo):Oxybutynin (27.2 mg/kg; p.o.; single) exhibits significant binding of mouse brain muscarinic receptors that about a 2-fold increase in Kd?values for specific [3H]N-methylscopolamine binding 0.5 and 2 h later.
  • In Vitro
    Oxybutynin (0.1, 0.3, 1, 3, 10, 30, 100 μM; 200 ms) inhibits vascular Kv channels in a concentration-dependent manner independent of anticholinergic effect in coronary arterial smooth muscle cells. Cell Viability Assay Cell Line:Coronary arterial smooth muscle cells (from male New Zealand White rabbits)Concentration:10 μM Incubation Time:200 ms Result:Rapidly inhibited the Kv current within 2 min and reduced the Kv current by 44% at +60 Mv.Inhibited the Kv current by changing the gating properties of Kv channels.Cell Viability Assay Cell Line:Coronary arterial smooth muscle cells (from male New Zealand White rabbits) Concentration:0.1, 0.3, 1, 3, 10, 30, 100 μM Incubation Time:200 ms Result:Reduced the Kv current amplitude in a concentration-dependent manner, with an IC50 value of 11.51 μM.
  • In Vivo
    Oxybutynin (27.2 mg/kg; p.o.; single) exhibits significant binding of mouse brain muscarinic receptors that about a 2-fold increase in Kd values for specific [3H]N-methylscopolamine binding 0.5 and 2 h later. Animal Model:Male ddY strain mice (9 to 13-week-old).Dosage:27.2 mg/kg (76.1 μmol/kg) Administration:Oral administration; single.Result:Significant increased Kd values for specific [3H]NMS binding in mouse bladder with values of 54.7% and 40.6% when at 0.5 and 2 hours, respectively.Significant increased Kd values for specific [3H]NMS binding in mouse cerebral cortex with values of 120% and 71.2% when at 0.5 and 2 hours, respectively.
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    AChR
  • Recptor
    mAChR
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    5633-20-5
  • Formula Weight
    357.49
  • Molecular Formula
    C22H31NO3
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 71 mg/mL (198.6 mM); DMSO: 71 mg/mL (198.6 mM)
  • SMILES
    CCN(CC)CC#CCOC(=O)C(O)(C1CCCCC1)C1=CC=CC=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ito Y, et al. Eur J Pharmacol. 2009 Aug 1;615(1-3):201-6.
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