Methoxyphenamine: Difference between revisions

	WikiDoc Resources for Methoxyphenamine
Articles
Most recent articles on Methoxyphenamine Most cited articles on Methoxyphenamine Review articles on Methoxyphenamine Articles on Methoxyphenamine in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Methoxyphenamine Images of Methoxyphenamine Photos of Methoxyphenamine Podcasts & MP3s on Methoxyphenamine Videos on Methoxyphenamine
Evidence Based Medicine
Cochrane Collaboration on Methoxyphenamine Bandolier on Methoxyphenamine TRIP on Methoxyphenamine
Clinical Trials
Ongoing Trials on Methoxyphenamine at Clinical Trials.gov Trial results on Methoxyphenamine Clinical Trials on Methoxyphenamine at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Methoxyphenamine NICE Guidance on Methoxyphenamine NHS PRODIGY Guidance FDA on Methoxyphenamine CDC on Methoxyphenamine
Books
Books on Methoxyphenamine
News
Methoxyphenamine in the news Be alerted to news on Methoxyphenamine News trends on Methoxyphenamine
Commentary
Blogs on Methoxyphenamine
Definitions
Definitions of Methoxyphenamine
Patient Resources / Community
Patient resources on Methoxyphenamine Discussion groups on Methoxyphenamine Patient Handouts on Methoxyphenamine Directions to Hospitals Treating Methoxyphenamine Risk calculators and risk factors for Methoxyphenamine
Healthcare Provider Resources
Symptoms of Methoxyphenamine Causes & Risk Factors for Methoxyphenamine Diagnostic studies for Methoxyphenamine Treatment of Methoxyphenamine
Continuing Medical Education (CME)
CME Programs on Methoxyphenamine
International
Methoxyphenamine en Espanol Methoxyphenamine en Francais
Business
Methoxyphenamine in the Marketplace Patents on Methoxyphenamine
Experimental / Informatics
List of terms related to Methoxyphenamine

Methoxyphenamine
Clinical data
AHFS/Drugs.com	International Drug Names
Routes of; administration	Oral
ATC code	R03CB02 (WHO) ;
Legal status
Legal status	In general: ℞ (Prescription only);
Identifiers
	IUPAC name 1-(2-methoxyphenyl)-N-methylpropan-2-amine;
CAS Number	93-30-1;
PubChem CID	4117;
ChemSpider	3974;
UNII	J3Z5SRI26Z;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C11H17NO
Molar mass	179.26 g/mol
3D model (JSmol)	Interactive image;
	SMILES CC(CC1=CC=CC=C1OC)NC;
	InChI 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;

VisualWikitext

Latest revision as of 16:42, 20 August 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Methoxyphenamine (trade names ASMI, Euspirol, Orthoxine, Ortodrinex, Proasma), also known as 2-methoxy-N-methyl amphetamine (OMMA), is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator.^[1]

Chemistry

Methoxyphenamine was first synthesized at the Upjohn company by Woodruff and co-workers.^[2] A later synthesis by Heinzelman, from the same company, corrects the m.p. given for methoxyphenamine hydrochloride in the earlier paper, and describes an improved synthetic procedure, as well as resolution of the racemic methoxyphenamine.^[3]

References

↑ Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. ISBN 3-88763-075-0.
↑ E. H. Woodruff, J. P. Lambooy and W. E. Burt (1940). "Physiologically active amines. III. Secondary and tertiary β-phenylpropylamines and β-phenylisopropylamines." J. Am. Chem. Soc. 62 922-924.
↑ R. V. Heinzelman (1953). "Physiologically active secondary amines. β-(o-Methoxyphenyl)-isopropyl-N-methylamine and related compounds." J. Am. Chem. Soc. 75 921-925.

Template:Phenethylamines

[isbn3-88763-075-0-1] 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] E. H. Woodruff, J. P. Lambooy and W. E. Burt (1940). "Physiologically active amines. III. Secondary and tertiary β-phenylpropylamines and β-phenylisopropylamines." J. Am. Chem. Soc. 62 922-924.

[3] R. V. Heinzelman (1953). "Physiologically active secondary amines. β-(o-Methoxyphenyl)-isopropyl-N-methylamine and related compounds." J. Am. Chem. Soc. 75 921-925.

[1]

[2]

[3]

Revision as of 15:56, 13 April 2015 (view source) Aparna Vuppala (talk \| contribs) No edit summary ← Older edit	Latest revision as of 16:42, 20 August 2015 (view source) WikiBot (talk \| contribs) m (Protected "Methoxyphenamine": Bot: Protecting all pages from category Drug ([Edit=Allow only administrators] (indefinite) [Move=Allow only administrators] (indefinite)))
(No difference)

Clinical data

AHFS/Drugs.com	International Drug Names
Routes of administration	Oral
ATC code	R03CB02 (WHO)
Legal status
Legal status	In general: ℞ (Prescription only)
Identifiers
IUPAC name 1-(2-methoxyphenyl)-N-methylpropan-2-amine
CAS Number	93-30-1
PubChem CID	4117
ChemSpider	3974
UNII	J3Z5SRI26Z
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C₁₁H₁₇NO
Molar mass	179.26 g/mol
3D model (JSmol)	Interactive image
SMILES CC(CC1=CC=CC=C1OC)NC
InChI 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: Difference between revisions

Latest revision as of 16:42, 20 August 2015

Overview

Chemistry

References

Navigation menu