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Details

Stereochemistry RACEMIC
Molecular Formula C13H21N3O3
Molecular Weight 267.3241
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBUTEROL

SMILES

CC(C)(C)NCC(O)C1=CC=C(O)C(NC(N)=O)=C1

InChI

InChIKey=KEMXXQOFIRIICG-UHFFFAOYSA-N
InChI=1S/C13H21N3O3/c1-13(2,3)15-7-11(18)8-4-5-10(17)9(6-8)16-12(14)19/h4-6,11,15,17-18H,7H2,1-3H3,(H3,14,16,19)

HIDE SMILES / InChI

Molecular Formula C13H21N3O3
Molecular Weight 267.3241
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Carbuterol is a beta-adrenergic bronchodilator with selectivity for bronchial smooth muscle relative to cardiac and vascular tissues of several species including man. In vitro studies demonstrated that carbuterol was a direct acting beta-adrenergic agonist, not dependent on endogenous catecholamine release, and was devoid of alpha-adrenergic agonist activity. The activity of the racemate was shown to reside primarily in the l-enantiomer. Carbuterol inhibited immunologically induced release of histamine and slow reacting substance of anaphylaxis from passively sensitized fragmented rhesus monkey lung and also inhibited passive cutaneous anaphylaxis in rats. Acute toxicity studies in mice, rats and guinea pigs indicated a wide safety margin for carbuterol. Carbuterol is a safer and more effective bronchodilator than ephedrine.

Approval Year

PubMed

PubMed

TitleDatePubMed
Generic sample preparation combined with high-resolution liquid chromatography-time-of-flight mass spectrometry for unification of urine screening in doping-control laboratories.
2010-04
A controversy that has been tough to swallow: is the treatment of achalasia now digested?
2010-02
Hydrophobicity-aided potentiometric detection of catecholamines, beta-agonists, and beta-blockers in a mixed-solvent capillary electrophoresis system.
2009-01
[Multi-residue analysis of 10 beta2-agonists in animal tissues using gas chromatography-mass spectrometry].
2008-01
Patents

Sample Use Guides

In Vivo Use Guide
2 mg dosage three times daily
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:20:23 GMT 2025
Edited
by admin
on Mon Mar 31 18:20:23 GMT 2025
Record UNII
0N12JR32MR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBUTEROL
INN   MI   WHO-DD  
INN  
Official Name English
CARBUTEROL [MI]
Preferred Name English
carbuterol [INN]
Common Name English
(5-(2-(TERT-BUTYLAMINO)-1-HYDROXYETHYL)-2-HYDROXYPHENYL)UREA
Systematic Name English
UREA, (5-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-2-HYDROXYPHENYL)-
Systematic Name English
Carbuterol [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QR03CC10
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
WHO-ATC R03AC10
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
NCI_THESAURUS C48149
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
WHO-ATC R03CC10
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
WHO-VATC QR03AC10
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
252-257-5
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
SMS_ID
100000084570
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
DRUG CENTRAL
506
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
DRUG BANK
DB13625
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
EVMPD
SUB06621MIG
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
MERCK INDEX
m3102
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY Merck Index
ChEMBL
CHEMBL2110780
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
INN
3360
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
NCI_THESAURUS
C79709
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
MESH
C100249
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
PUBCHEM
36976
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
FDA UNII
0N12JR32MR
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
CAS
34866-47-2
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID00865737
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
WIKIPEDIA
CARBUTEROL
Created by admin on Mon Mar 31 18:20:23 GMT 2025 , Edited by admin on Mon Mar 31 18:20:23 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY