Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C9H15BrN2O2.ClH |
| Molecular Weight | 299.593 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C)(C)NCC(O)C1=CC(Br)=NO1
InChI
InChIKey=JILLNVBIEKMQLV-UHFFFAOYSA-N
InChI=1S/C9H15BrN2O2.ClH/c1-9(2,3)11-5-6(13)7-4-8(10)12-14-7;/h4,6,11,13H,5H2,1-3H3;1H
| Molecular Formula | C9H15BrN2O2 |
| Molecular Weight | 263.132 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
| 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 |
Broxaterol is a β2 adrenoreceptor agonist used for the treatment of respiratory disease. Broxaterol produced a significant clinical improvement, an increase in FEV1 and a decrease in supplemental anti-asthmatic drugs used in patients with reversible airflow obstruction and in asthmatic children. The increases in FEV1 versus baseline were significantly maintained after the end of the treatment. Prompt disappearance of the asthmatic attack with significant improvement in lung function was observed in children. In two long-term controlled trials, the respiratory effects of broxaterol nebulizer solution were significantly greater than placebo. Moreover, broxaterol by metered dose inhaler was more effective than salbutamol after 3 months follow-up, showing the absence of tachyphylaxis. In long-term clinical evaluation, broxaterol has been shown to be well tolerated, with an incidence of adverse reactions equal to or less than that reported in the literature for other beta 2-agonists. The side effects most frequently associated with broxaterol were tremor, nervousness, and palpitations.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2572038
0.6-1.2 mg/day by metered dose inhaler or 0.5-1.5 mg/day orally, from 2 weeks to 1 year
Route of Administration:
Other
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:13:17 GMT 2025
by
admin
on
Mon Mar 31 23:13:17 GMT 2025
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| Record UNII |
19BN8D5HET
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| Record Status |
Validated (UNII)
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| Record Version |
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278-496-5
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19BN8D5HET
Created by
admin on Mon Mar 31 23:13:17 GMT 2025 , Edited by admin on Mon Mar 31 23:13:17 GMT 2025
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190536
Created by
admin on Mon Mar 31 23:13:17 GMT 2025 , Edited by admin on Mon Mar 31 23:13:17 GMT 2025
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76596-58-2
Created by
admin on Mon Mar 31 23:13:17 GMT 2025 , Edited by admin on Mon Mar 31 23:13:17 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |