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
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
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
Title | Date | PubMed |
---|---|---|
[Multi-residue analysis of 10 beta2-agonists in animal tissues using gas chromatography-mass spectrometry]. | 2008 Jan |
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Hydrophobicity-aided potentiometric detection of catecholamines, beta-agonists, and beta-blockers in a mixed-solvent capillary electrophoresis system. | 2009 Jan |
|
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/368368
2 mg dosage three times daily
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:25:22 GMT 2023
by
admin
on
Fri Dec 15 15:25:22 GMT 2023
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Record UNII |
G8F3U654FU
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Record Status |
Validated (UNII)
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Record Version |
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-
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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
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Code System | Code | Type | Description | ||
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36975
Created by
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C81650
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PRIMARY | |||
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DTXSID60956352
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PRIMARY | |||
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100000084872
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PRIMARY | |||
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34866-46-1
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PRIMARY | |||
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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
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PRIMARY | Merck Index | ||
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SUB01054MIG
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252-255-4
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PRIMARY | |||
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CHEMBL2110780
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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
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |