Cat. No. 0634
Chemical Name: α1-[[(1,1-Dimethylethyl)amino]methyl
Biological ActivityNon-selective β-adrenergic agonist, more potent at β2 than β1 receptors.
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Certificate of Analysis / Product Datasheet / Safety Datasheet
January et al (1998) Salmeterol-induced desensitisation, internalization and phosphorylation of the human β2-adrenoceptor. Br.J.Pharmacol. 123 701. PMID: 9517390.
Prior et al (1998) Effects of the enantiomers of R,S-salbutamol on incompletely fused tetanic contractions of slow- and fast-twitch skeletal muscles of the guinea-pig. Br.J.Pharmacol. 123 558. PMID: 9504397.
Strosberg and Pietri-Rouxel (1996) Function and regulation of the β3-adrenoceptor. TiPS 17 373. PMID: 8979772.
Merck Index 12 217.
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Citations are publications that use Tocris products. Selected citations for Salbutamol hemisulfate include:
Namkung et al (2016) Monitoring G protein-coupled receptor and [beta]-arrestin trafficking in live cells using enhanced bystander BRET Nature Communications 7 12178. PMID: 27397672.
Sykes and Charlton (2012) Slow receptor dissociation is not a key factor in the duration of action of inhaled long-acting β2-adrenoceptor agonists. Br J Pharmacol 165 2672. PMID: 21883146.
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Keywords: Salbutamol hemisulfate, supplier, β-adrenoceptor, beta-adrenoceptor, b-adrenoceptor, agonists, β-adrenergic, beta-adrenergic, b-adrenergic, Receptors, albuterol, Tocris Bioscience, Adrenergic β2 Receptor Agonist products
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