Catalog Number: 0634
Chemical Name: α1-[[(1,1-Dimethylethyl)amino]methyl]-4-hydroxy-1,3-benzenedimethanol hemisulfate
Biological Activity
Non-selective β-adrenergic agonist, more potent at β2 than β1 receptors.
Technical Data
  • M.Wt:
    288.35
  • Formula:
    C13H21NO3.1/2H2SO4
  • Solubility:
    Soluble to 100 mM in water
  • Purity:
    >99%
  • Storage:
    Store at RT
  • CAS No:
    51022-70-9
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.
Background References

  1. Kishimoto T et al.
    Leucocyte Typing VI. Garland Publishing Inc. London.
  2. Function and regulation of the β3-adrenoceptor.
    Strosberg and Pietri-Rouxel
    TiPS, 1996;17:373
  3. Salmeterol-induced desensitisation, internalization and phosphorylation of the human β2-adrenoceptor.
    January et al.
    Br.J.Pharmacol., 1998;123:701
  4. Effects of the enantiomers of R,S-salbutamol on incompletely fused tetanic contractions of slow- and fast-twitch skeletal muscles of the guinea-pig.
    Prior et al.
    Br.J.Pharmacol., 1998;123:558
Citations:

The citations listed below are publications that use Tocris products. Selected citations for Salbutamol hemisulfate include:

2 Citations: Showing 1 - 2
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  1. Monitoring G protein-coupled receptor and [beta]-arrestin trafficking in live cells using enhanced bystander BRET
    Authors: Namkung Et al.
    Nature Communications 2016;7:12178
  2. Slow receptor dissociation is not a key factor in the duration of action of inhaled long-acting β2-adrenoceptor agonists.
    Authors: Sykes and Charlton
    Br J Pharmacol 2012;165:2672

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