Date published: 2025-9-17

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Oxyfedrine (CAS 15687-41-9)

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Alternate Names:
3-[[(1S,2R)-2-Hydroxy-1-methyl-2-phenylethyl]amino]-1-(3-methoxyphenyl)-1-propanone
CAS Number:
15687-41-9
Molecular Weight:
313.39
Molecular Formula:
C19H23NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Oxyfedrine is a synthetic compound that has been explored for various applications. Its chemical structure allow it to interact with different biological pathways, making it a subject of interest in biochemical research. Compounds like oxyfedrine are studied for their potential effects on metabolic processes and cellular functions. Oxyfedrine′s interactions with cellular receptors and enzymes could provide valuable information on the modulation of various biological activities. Additionally, oxyfedrine′s molecular framework makes it a candidate for chemical studies focused on understanding the relationship between molecular structure and biological activity.


Oxyfedrine (CAS 15687-41-9) References

  1. Positive and negative chronotropic response of the S-A node to oxyfedrine.  |  Sakai, K., et al. 1975. Jpn J Pharmacol. 25: 573-81. PMID: 1221139
  2. Excretion of norephedrine by man after oral administration of oxyfedrine.  |  Appel, E., et al. 1975. Eur J Clin Pharmacol. 8: 161-6. PMID: 1233214
  3. Antimicrobial potentiality of a new non-antibiotic: the cardiovascular drug oxyfedrine hydrochloride.  |  Mazumdar, K., et al. 2003. Microbiol Res. 158: 259-64. PMID: 14521236
  4. In vitro and in vivo synergism between tetracycline and the cardiovascular agent oxyfedrine HCl against common bacterial strains.  |  Mazumdar, K., et al. 2005. Biol Pharm Bull. 28: 713-7. PMID: 15802815
  5. Effects of oxyfedrine on regional myocardial blood flow in patients with coronary artery disease.  |  Kaski, JC., et al. 1991. Cardiovasc Drugs Ther. 5: 991-6. PMID: 1801897
  6. Vasodilator oxyfedrine inhibits aldehyde metabolism and thereby sensitizes cancer cells to xCT-targeted therapy.  |  Otsuki, Y., et al. 2020. Cancer Sci. 111: 127-136. PMID: 31692172
  7. Recent progress in the chemistry of β-aminoketones.  |  Hammouda, MM. and Elattar, KM. 2022. RSC Adv. 12: 24681-24712. PMID: 36128366
  8. The effect of prolonged treatment with oxyfedrine on intracellular potentials and on other features of cardiac function in rabbits and guinea-pigs.  |  Polster, P. and Vaughan Williams, EM. 1973. Br J Pharmacol. 47: 187-95. PMID: 4146572
  9. Effects of oxyfedrine on isolated portal vein and other smooth muscles.  |  Mackenzie, JE. and Parratt, JR. 1973. Br J Pharmacol. 47: 827-37. PMID: 4146743
  10. The haemodynamic effects of prolonged oral administration of oxyfedrine, a partial agonist at beta-adrenoceptors: comparison with propranolol.  |  Parratt, JR. 1974. Br J Pharmacol. 51: 5-13. PMID: 4155336
  11. [Mechanism of action of oxyfedrine as a partial beta receptor agonist].  |  Sternitzke, N., et al. 1984. Z Kardiol. 73: 586-93. PMID: 6095552
  12. [The action of oxyfedrine on haemodynamics, inotropism and blood perfusion of the partially ischaemic myocardium after digoxin premedication. Studies on anaesthetized dogs (author's transl)].  |  Hahn, N., et al. 1981. Arzneimittelforschung. 31: 410-4. PMID: 7194664
  13. Echocardiographic evaluation of acute administration of oxyfedrine in patients with coronary artery disease.  |  Maione, S., et al. 1981. Curr Med Res Opin. 7: 241-6. PMID: 7226873

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Oxyfedrine, 10 mg

sc-477590
10 mg
$630.00