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
SMILES
CC(C)(C)NCC(O)C1=CC(NC(N)=O)=C(O)C=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)
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
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 16:09:15 UTC 2023
by
admin
on
Fri Dec 15 16:09:15 UTC 2023
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Record UNII |
0N12JR32MR
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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WHO-VATC |
QR03CC10
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WHO-ATC |
R03AC10
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NCI_THESAURUS |
C48149
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WHO-ATC |
R03CC10
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WHO-VATC |
QR03AC10
Created by
admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
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Code System | Code | Type | Description | ||
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252-257-5
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100000084570
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506
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DB13625
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SUB06621MIG
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m3102
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PRIMARY | Merck Index | ||
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CHEMBL2110780
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3360
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C79709
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C100249
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36976
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0N12JR32MR
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34866-47-2
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DTXSID00865737
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CARBUTEROL
Created by
admin on Fri Dec 15 16:09:15 UTC 2023 , Edited by admin on Fri Dec 15 16:09:15 UTC 2023
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |