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Details

Stereochemistry RACEMIC
Molecular Formula C13H18ClF3N2O
Molecular Weight 310.743
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MABUTEROL

SMILES

CC(C)(C)NCC(O)C1=CC(Cl)=C(N)C(=C1)C(F)(F)F

InChI

InChIKey=JSJCTEKTBOKRST-UHFFFAOYSA-N
InChI=1S/C13H18ClF3N2O/c1-12(2,3)19-6-10(20)7-4-8(13(15,16)17)11(18)9(14)5-7/h4-5,10,19-20H,6,18H2,1-3H3

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/6152155

Mabuterol is a long acting βeta 2-adrenergic agonist which stimulates adenylyl cyclase activity and the closing of calcium channels. Studies indicate that the R enantiomer of mabuterol is more potent than the S enantiomer. In addition, the half-life is longer in the R enantiomer than the S. Studies conducted on rats and dogs show that mabuterol acts as a bronchodilator. At high concentrations mabuterol can also antagonize beta1 adrenoceptors in guinea pigs

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Use of molecularly imprinted polymers in the solid-phase extraction of clenbuterol from animal feeds and biological matrices.
2001 Aug 5
Integrated acquisition of analytical and biopharmaceutical screening data for beta-adrenergic-drugs employing diversified macrocycle supported potentiometric detection in HPLC systems.
2002 Aug
Improvement in steroid screening for doping control with special emphasis on stanozolol.
2003 Jan 24
Determination of beta-agonists in liver and retina by liquid chromatography-tandem mass spectrometry.
2005 Jan-Feb
Determination of beta-agonist residues in bovine urine using liquid chromatography-tandem mass spectrometry.
2005 Jan-Feb
Enantioselective pharmacokinetics of mabuterol in rats studied using sequential achiral and chiral HPLC.
2005 Nov
Application of an enzyme-linked immunosorbent assay for the detection of clenbuterol residues in swine urine and feeds.
2007 Feb
Enantiomeric separation of beta2-agonists on macrocyclic antibiotic chiral stationary phases in high performance liquid chromatography.
2007 Nov
Validation of radioimmunoassay screening methods for beta-agonists in bovine liver according to Commission Decision 2002/657/EC.
2008 Dec
Simultaneous enantioseparation of four beta2-agonists by capillary electrophoresis with cyclodextrin additives. Study of the enantioselective mechanism.
2008 Dec
[Multi-residue analysis of 10 beta2-agonists in animal tissues using gas chromatography-mass spectrometry].
2008 Jan
How to decrease ion suppression in a multiresidue determination of beta-agonists in animal liver and urine by liquid chromatography-mass spectrometry with ion-trap detector.
2009 Apr 1
Generic sample preparation combined with high-resolution liquid chromatography-time-of-flight mass spectrometry for unification of urine screening in doping-control laboratories.
2010 Apr
[Determination of fifteen beta-agonists in animal urine by high performance liquid chromatography-tandem mass spectrometry].
2010 Aug
Development and validation of a liquid chromatography tandem mass spectrometry method for the analysis of beta-agonists in animal feed and drinking water.
2010 Sep 24
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
MABUTEROL
INN   MART.   MI   WHO-DD  
INN  
Official Name English
MABUTEROL [MI]
Common Name English
MABUTEROL [MART.]
Common Name English
Mabuterol [WHO-DD]
Common Name English
4-AMINO-.ALPHA.-((TERT-BUTYLAMINO)METHYL)-3-CHLORO-5-(TRIFLUOROMETHYL)BENZYL ALCOHOL
Systematic Name English
mabuterol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
Code System Code Type Description
PUBCHEM
3995
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
MESH
C044573
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
EVMPD
SUB08631MIG
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
SMS_ID
100000081736
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
INN
5089
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
MERCK INDEX
m6973
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL86749
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
WIKIPEDIA
MABUTEROL
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
DRUG CENTRAL
1623
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
FDA UNII
R4K19W6S7Q
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
NCI_THESAURUS
C81647
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
CAS
56341-08-3
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID3048283
Created by admin on Fri Dec 15 17:37:31 GMT 2023 , Edited by admin on Fri Dec 15 17:37:31 GMT 2023
PRIMARY