Oxybutynin MedChemExpress (MCE)

Product Name	oxybutynin
Synonyms	OXYBUTININ oxybutynin Oxibutynin 4-diethylamino-2-butynylalpha-phenylcyclohexaneglycolate alpha-phenyl-cyclohexaneglycolicaci4-(diethylamino)-2-butynylester 4-(diethylaMino)but-2-yn-1-yl 2-cyclohexyl-2-hydroxy-2-phenylacetate Synonyms OXYBUTININ oxybutynin Oxibutynin 4-diethylamino-2-butynylalpha-phenylcyclohexaneglycolate alpha-phenyl-cyclohexaneglycolicaci4-(diethylamino)-2-butynylester 4-(diethylaMino)but-2-yn-1-yl 2-cyclohexyl-2-hydroxy-2-phenylacetate alpha-cyclohexyl-alpha-hydroxy-benzeneaceticaci4-(diethylamino)-2-butynyl α-cyclohexyl-α-hydroxy-benzeneacetic acid-4-(diethylamino)-2-butyn-1-yl ester Benzeneacetic acid, a-cyclohexyl-a-hydroxy-,4-(diethylaMino)-2-butyn-1-yl ester Benzeneacetic acid, alpha-cyclohexyl-alpha-hydroxy-, 4-(diethylamino)-2-butynyl ester
CAS	5633-20-5
EINECS	630-332-7
Chemical Formula	C22H31NO3
Molecular Weight	357.49
inchi	InChI=1/C22H31NO3/c1-3-23(4-2)17-11-12-18-26-21(24)22(25,19-13-7-5-8-14-19)20-15-9-6-10-16-20/h5,7-8,13-14,20,25H,3-4,6,9-10,15-18H2,1-2H3
Package	10 mM * 1 mL;100 mg;500 mg
Price	Email to quote
Descriptions	Oxybutynin Oxybutynin MedChemExpress (MCE) HY-B0267 5633-20-5 99.55% Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year Room temperature in continental US Descriptions Oxybutynin Oxybutynin MedChemExpress (MCE) HY-B0267 5633-20-5 99.55% Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year Room temperature in continental US may vary elsewhere. Oxybutynin is an anticholinergic agent, which inhibits vascular Kv channels in a concentration-dependent manner, with an IC50 of 11.51 μM. Oxybutynin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. 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[1]. 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[2]. \| \| \| \| \| \| \| \| \| \| [1]. Li H, et al. The anticholinergic drug oxybutynin inhibits voltage-dependent K+ channels in coronary arterial smooth muscle cells. Clin Exp Pharmacol Physiol. 2019 Nov 46(11):1030-1036. [Content Brief] [2]. Oki T, et al. Comparative evaluation of central muscarinic receptor binding activity by oxybutynin, tolterodine and darifenacin used to treat overactive bladder. J Urol. 2007 Feb 177(2):766-70. [Content Brief]
Last Update	2025-04-01 14:45:47

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