Procaterol

CAT:
804-HY-114732
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Procaterol - image 1

Procaterol

  • Description:

    Procaterol is an oral selective β2 adrenergic receptor agonist. Procaterol inhibits eosinophil migration and the release of eosinophil chemotactic factor from BEAS-2B cells through a cyclic AMP-dependent mechanism. Procaterol has a large dose difference existing between the bronchodilator effect and the anabolic effect in rat, can be used for asthma research in athletes[1].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302-H312-H332
  • Target:

    Adrenergic Receptor
  • Type:

    Reference compound
  • Related Pathways:

    GPCR/G Protein; Neuronal Signaling
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Others
  • Assay Protocol:

    https://www.medchemexpress.com/procaterol.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O[C@@H](C(C=C1)=C(C=CC2=O)C(N2)=C1O)[C@@H](CC)NC(C)C
  • Molecular Formula:

    C16H22N2O3
  • Molecular Weight:

    290.36
  • Precautions:

    P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
  • References & Citations:

    [1]Ikezono K, et al. Bronchodilating effect and anabolic effect of inhaled procaterol. Int J Sports Med. 2008 Nov;29 (11) :888-94. |[2]Tashimo H, et al. Effect of procaterol, a beta (2) selective adrenergic receptor agonist, on airway inflammation and hyperresponsiveness. Allergol Int. 2007 Sep;56 (3) :241-7. |[3]Koyama S, et al. Procaterol inhibits IL-1beta- and TNF-alpha-mediated epithelial cell eosinophil chemotactic activity. Eur Respir J. 1999 Oct;14 (4) :767-75. |[4]Yamaya M, et al. Procaterol inhibits rhinovirus infection in primary cultures of human tracheal epithelial cells. Eur J Pharmacol. 2011 Jan 10;650 (1) :431-44. |[5]Komatani-Tamiya N, et al. Procaterol-stimulated increases in ciliary bend amplitude and ciliary beat frequency in mouse bronchioles. Cell Physiol Biochem. 2012;29 (3-4) :511-22.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Phase 4
  • Isoform:

    β adrenergic receptor
  • CAS Number:

    [72332-33-3]