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
| Size | Price / USD | Stock | Quantity |
| 100MG | 42 | In Stock |
|
| 200MG | 58 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameOxybutynin
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NoteResearch use only, not for human use.
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Brief DescriptionOxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties.
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DescriptionOxybutynin 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.
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In VitroOxybutynin (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.
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In VivoOxybutynin (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.
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetAChR
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RecptormAChR
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number5633-20-5
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Formula Weight357.49
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Molecular FormulaC22H31NO3
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Purity>98% (HPLC)
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SolubilityEthanol: 71 mg/mL (198.6 mM); DMSO: 71 mg/mL (198.6 mM)
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SMILESCCN(CC)CC#CCOC(=O)C(O)(C1CCCCC1)C1=CC=CC=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Ito Y, et al. Eur J Pharmacol. 2009 Aug 1;615(1-3):201-6.
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