Zinterol hydrochloride
Discontinued Product
Chemical Name: N-[5-[2-[(1,1-Dimethyl-2-phenylethyl)amino]-1-hydroxyethyl]-2-hydroxyphenyl]methanesulphonamide hydrochloride
Purity: ≥98%
Biological Activity
Zinterol hydrochloride is a potent and selective β2-adrenoceptor agonist (pKB values are 8.3 and < 5.7 for β 2 and β1 receptors respectively, as measured in human artery).Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Beta-2 adrenergic activation of L-type Ca2+ current in cardiac myocytes.
Arvydas Skeberdis et al.
J.Pharmacol.Exp.Ther., 1997;283:452 -
Four β-adrenoceptor subtypes in the mammalian heart.
Kauman
TiPS, 1997;18:70 -
Agonist effects of zinterol at the mouse and human β3-adrenoceptor.
Hutchinson et al.
Naunyn Schmiedebergs Arch.Pharmacol., 2006;373:158
Product Datasheets
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Citations for Zinterol hydrochloride
The citations listed below are publications that use Tocris products. Selected citations for Zinterol hydrochloride include:
4 Citations: Showing 1 - 4
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ADRB2 polymorphism Arg16Gly modifies the natural outcome of heart failure and dictates therapeutic response to β-blockers in patients with heart failure.
Authors: Huang Et al.
Cell Discov 2018;4:57
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Caveolae compartmentalise β2-adrenoceptor signals by curtailing cAMP production and maintaining phosphatase activity in the sarcoplasmic reticulum of the adult ventricular myocyte.
Authors: Macdougall Et al.
J Mol Cell Cardiol 2012;52:388
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Stress and glucocorticoids impair memory retrieval via β2-adrenergic, Gi/o-coupled suppression of cAMP signaling.
Authors: Schutsky Et al.
J Neurosci 2011;31:14172
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A2B adenosine receptor signaling attenuates acute lung injury by enhancing alveolar fluid clearance in mice.
Authors: Eckle Et al.
J Am Coll Cardiol 2008;118:3301
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