Oxybutynin hydrochloride
CAS No. 1508-65-2
Oxybutynin hydrochloride( MJ4309-1 )
Catalog No. M12107 CAS No. 1508-65-2
Oxybutynin is also a possible treatment of hyperhidrosis (hyper-active sweating) .
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | 27 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 54 | In Stock |
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| 1G | 79 | In Stock |
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Biological Information
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Product NameOxybutynin hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionOxybutynin is also a possible treatment of hyperhidrosis (hyper-active sweating) .
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DescriptionOxybutynin is also a possible treatment of hyperhidrosis (hyper-active sweating) .(In Vitro):Oxybutynin chloride (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 chloride (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 chloride (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 chloride (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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SynonymsMJ4309-1
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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 Number1508-65-2
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Formula Weight393.96
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Molecular FormulaC22H32ClNO3
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Purity>98% (HPLC)
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SolubilityEthanol: 79 mg/mL (200.53 mM); Water: 4 mg/mL (10.15 mM); DMSO: 79 mg/mL (200.53 mM)
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SMILESO=C(OCC#CCN(CC)CC)C(O)(C1CCCCC1)C2=CC=CC=C2.[H]Cl
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Chemical Name4-Diethylaminobut-2-ynyl 2-cyclohexyl-2-hydroxy-2-phenylethanoate Hydrochloride
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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