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Details

Stereochemistry RACEMIC
Molecular Formula C11H17NO
Molecular Weight 179.2588
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHOXYPHENAMINE

SMILES

CNC(C)CC1=C(OC)C=CC=C1

InChI

InChIKey=OEHAYUOVELTAPG-UHFFFAOYSA-N
InChI=1S/C11H17NO/c1-9(12-2)8-10-6-4-5-7-11(10)13-3/h4-7,9,12H,8H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C11H17NO
Molecular Weight 179.2588
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Methoxyphenamine also known as 2-methoxy-N-methylamphetamine (OMMA), is a beta adrenergic receptor agonist nd is used as a bronchodilator to treat asthma, chronic obstructive pulmonary disease (COPD) and postinfectious cough. In addition, methoxyphenamine using is prohibited in sports according to the regulations of the World Anti-Doping Agency (WADA).

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
157 ng/mL
60.3 mg single, oral
dose: 60.3 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXYPHENAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
1315 ng × h/mL
60.3 mg single, oral
dose: 60.3 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXYPHENAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
2 h
60.3 mg single, oral
dose: 60.3 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
METHOXYPHENAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: FASTED
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer
Drug as victim
PubMed

PubMed

TitleDatePubMed
Chromatographic analysis of phenethylamine-antihistamine combinations using C8, C18 or cyano columns and micellar sodium dodecyl sulfate-pentanol mixtures.
2001 Apr
Anti-inflammatory effect of methoxyphenamine compound in rat model of chronic obstructive pulmonary disease.
2003 Dec
Microchip-based liquid-liquid extraction for gas-chromatography analysis of amphetamine-type stimulants in urine.
2006 Sep 29
Doping control analysis of methoxyphenamine using liquid chromatography-tandem mass spectrometry.
2008
Induction of metamorphosis of pediveliger larvae of the mussel Mytilus galloprovincialis Lamarck, 1819 using neuroactive compounds, KCl, NH4Cl and organic solvents.
2008
Patents

Sample Use Guides

Unknown
Route of Administration: Oral
In Vitro Use Guide
It was revealed, that methoxyphenamine antagonizes the effects of histamine both in vivo and in vitro. In vitro studies indicate a noncompetitive antagonism. Histamine-induced contractions of the isolated guinea-pig ileum were antagonized by methoxyphenamine (10(-5) to 10(-3) M). The histamine log-concentration-response curve was shifted to the right in a parallel manner by methoxyphenamine (10(-5) to 10(-4) M), without depression of maximum responses. However, at higher concentrations, maximum responses were reduced. The slope of the Schild plot was significantly different from -1. The degree of the rightward shift of the concentration-response curves to histamine, produced by 10(-5) M of methoxyphenamine [3.90-(2.83, 4.97) fold], was not significantly different from that produced by 3 x 10(-9) M of mepyramine [4.60-(2.86, 6.52) fold]. Methoxyphenamine, at concentrations of 10(-5) to 3 x 10(-4) M, had no significant effect on responses of guinea-pig ilea to acetylcholine (10(-9) to 10(-5) M).
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:30:26 GMT 2023
Edited
by admin
on Sat Dec 16 16:30:26 GMT 2023
Record UNII
J3Z5SRI26Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHOXYPHENAMINE
INN   MI   WHO-DD  
INN  
Official Name English
O-METHOXY-N,.ALPHA.-DIMETHYLPHENETHYLAMINE
Common Name English
METHOXYPHENAMINE [MI]
Common Name English
Methoxyphenamine [WHO-DD]
Common Name English
BENZENEETHANAMINE, 2-METHOXY-N,.ALPHA.-DIMETHYL-
Systematic Name English
methoxyphenamine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
WHO-ATC R03CB02
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
WHO-VATC QR03CB02
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
Code System Code Type Description
DRUG BANK
DB13624
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
EVMPD
SUB08860MIG
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
SMS_ID
100000081437
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
ChEMBL
CHEMBL2010507
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
RXCUI
29704
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY RxNorm
FDA UNII
J3Z5SRI26Z
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
DRUG CENTRAL
1755
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
CAS
93-30-1
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
MESH
C005157
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID0023292
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
WIKIPEDIA
Methoxyphenamine
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
PUBCHEM
4117
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
INN
137
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
MERCK INDEX
m7341
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY Merck Index
CHEBI
134817
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
NCI_THESAURUS
C83958
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-237-7
Created by admin on Sat Dec 16 16:30:27 GMT 2023 , Edited by admin on Sat Dec 16 16:30:27 GMT 2023
PRIMARY
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SALT/SOLVATE -> PARENT
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METABOLITE -> PARENT
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ACTIVE MOIETY