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Deterenol

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(Redirected fromIsopropyloctopamine)
Deterenol
Clinical data
Trade namesBetafrine
Other namesIsopropylnorsynephrine, Isopropyloctopamine
Identifiers
  • 4-[1-hydroxy-2-(propan-2-ylamino)ethyl]phenol
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H17NO2
Molar mass195.262g·mol−1
3D model (JSmol)
  • CC(C)NCC(C1=CC=C(C=C1)O)O
  • InChI=1S/C11H17NO2/c1-8(2)12-7-11(14)9-3-5-10(13)6-4-9/h3-6,8,11-14H,7H2,1-2H3
  • Key:MPCPSVWSWKWJLO-UHFFFAOYSA-N

Deterenol(also known asIsopropylnorsynephrineandIsopropyloctopamine;trade nameBetaphrine) is astimulantdrug which acts as abeta agonist.It has been found as an ingredient ofdietary supplementproducts, but is banned in most countries due to risk ofcardiac arrest.[1][2][3][4][5]

See also

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References

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  1. ^Anderson WG (June 1983). "The sympathomimetic activity of N-isopropyloctopamine in vitro".The Journal of Pharmacology and Experimental Therapeutics.225(3): 553–8.PMID6306210.
  2. ^Mercader J, Wanecq E, Chen J, Carpéné C (September 2011). "Isopropylnorsynephrine is a stronger lipolytic agent in human adipocytes than synephrine and other amines present in Citrus aurantium".Journal of Physiology and Biochemistry.67(3): 443–52.doi:10.1007/s13105-011-0078-2.PMID21336650.S2CID22449550.
  3. ^Venhuis B, Keizers P, van Riel A, de Kaste D (June 2014). "A cocktail of synthetic stimulants found in a dietary supplement associated with serious adverse events".Drug Testing and Analysis.6(6): 578–81.doi:10.1002/dta.1664.PMID24802503.
  4. ^Zhao J, Wang M, Avula B, Khan IA (March 2018)."Detection and quantification of phenethylamines in sports dietary supplements by NMR approach".Journal of Pharmaceutical and Biomedical Analysis.151:347–355.doi:10.1016/j.jpba.2018.01.025.PMID29413984.S2CID46837518.
  5. ^Cohen PA, Travis JC, Vanhee C, Ohana D, Venhuis BJ (March 2021)."Nine prohibited stimulants found in sports and weight loss supplements: deterenol, phenpromethamine (Vonedrine), oxilofrine, octodrine, beta-methylphenylethylamine (BMPEA), 1,3-dimethylamylamine (1,3-DMAA), 1,4-dimethylamylamine (1,4-DMAA), 1,3-dimethylbutylamine (1,3-DMBA) and higenamine".Clinical Toxicology.59(11): 975–981.doi:10.1080/15563650.2021.1894333.PMID33755516.