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Details

Stereochemistry RACEMIC
Molecular Formula C13H21N3O3.ClH
Molecular Weight 303.785
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBUTEROL HYDROCHLORIDE

SMILES

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

InChI

InChIKey=QHWYYBXPBFQGNI-UHFFFAOYSA-N
InChI=1S/C13H21N3O3.ClH/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);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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 Apr
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 Fri Dec 15 15:25:22 GMT 2023
Edited
by admin
on Fri Dec 15 15:25:22 GMT 2023
Record UNII
G8F3U654FU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBUTEROL HYDROCHLORIDE
MART.   MI   USAN   WHO-DD  
USAN  
Official Name English
Carbuterol hydrochloride [WHO-DD]
Common Name English
CARBUTEROL HYDROCHLORIDE [USAN]
Common Name English
[5-[2-(tert-Butylamino)-1-hydroxyethyl]-2-hydroxyphenyl]urea monohydrochloride
Systematic Name English
CARBUTEROL HYDROCHLORIDE [MI]
Common Name English
SK&F 40383
Code English
CARBUTEROL HCL
Common Name English
UREA, (5-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-2-HYDROXYPHENYL)-, MONOHYDROCHLORIDE
Common Name English
SK&F-40383
Code English
CARBUTEROL HYDROCHLORIDE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
Code System Code Type Description
PUBCHEM
36975
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
NCI_THESAURUS
C81650
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID60956352
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
SMS_ID
100000084872
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
CAS
34866-46-1
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
MERCK INDEX
m3102
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY Merck Index
EVMPD
SUB01054MIG
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
ECHA (EC/EINECS)
252-255-4
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110780
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
FDA UNII
G8F3U654FU
Created by admin on Fri Dec 15 15:25:22 GMT 2023 , Edited by admin on Fri Dec 15 15:25:22 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY