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Methoxyphenamine

From Wikipedia, the free encyclopedia
Pair of enantiomers
Pharmaceutical compound
Methoxyphenamine
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 1-(2-methoxyphenyl)-N-methylpropan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.002.035Edit this at Wikidata
Chemical and physical data
FormulaC11H17NO
Molar mass179.263 g·mol−1
3D model (JSmol)
  • CC(CC1=CC=CC=C1OC)NC
  • InChI=1S/C11H17NO/c1-9(12-2)8-10-6-4-5-7-11(10)13-3/h4-7,9,12H,8H2,1-3H3
  • Key:OEHAYUOVELTAPG-UHFFFAOYSA-N

Methoxyphenamine (trade namesASMI,Euspirol,Orthoxine,Ortodrinex,Proasma), also known as2-methoxy-N-methylamphetamine (OMMA), is aβ-adrenergic receptoragonist of theamphetamine class used as abronchodilator.[1]

It acts as ananti-inflammatory in rats.[2]

Chemistry

[edit]

Methoxyphenamine was first synthesized at the Upjohn company by Woodruff and co-workers.[3] A later synthesis by Heinzelman, from the same company, corrects the melting point given for methoxyphenamine hydrochloride in the earlier paper, and describes an improved synthetic procedure, as well as resolution of theracemic methoxyphenamine.[4]

See also

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References

[edit]
  1. ^Swiss Pharmaceutical Society (2000).Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers.ISBN 3-88763-075-0.
  2. ^Wang YH, Bai CX, Hong QY, Chen J (December 2003)."Anti-inflammatory effect of methoxyphenamine compound in rat model of chronic obstructive pulmonary disease".Acta Pharmacologica Sinica.24 (12):1324–7.PMID 14653967.
  3. ^Woodruff EH, Lambooy JP, Burt WE (April 1940). "Physiologically active amines. III. Secondary and tertiary β-phenylpropylamines and β-phenylisopropylamines".Journal of the American Chemical Society.62 (4):922–4.Bibcode:1940JAChS..62..922W.doi:10.1021/ja01861a060.
  4. ^Heinzelman RV (February 1953). "Physiologically active secondary amines. β-(o-Methoxyphenyl)-isopropyl-N-methylamine and related compounds".Journal of the American Chemical Society.75 (4):921–5.Bibcode:1953JAChS..75..921H.doi:10.1021/ja01100a043.
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
Miscellaneous


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