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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
Structure of BROXATEROL HYDROCHLORIDE

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

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 C9H15BrN2O2
Molecular Weight 263.132
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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

Sources: JP 55108862

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative pharmacology of human beta-adrenergic receptor subtypes--characterization of stably transfected receptors in CHO cells.
2004 Feb
Novel mutants of the human beta1-adrenergic receptor reveal amino acids relevant for receptor activation.
2006 Jun 30
Patents

Patents

Sample Use Guides

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 Sat Dec 16 10:24:42 GMT 2023
Edited
by admin
on Sat Dec 16 10:24:42 GMT 2023
Record UNII
19BN8D5HET
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BROXATEROL HYDROCHLORIDE
Common Name English
5-ISOXAZOLEMETHANOL, 3-BROMO-.ALPHA.-(((1,1-DIMETHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
BROXATEROL HYDROCHLORIDE, (±)-
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
278-496-5
Created by admin on Sat Dec 16 10:24:42 GMT 2023 , Edited by admin on Sat Dec 16 10:24:42 GMT 2023
PRIMARY
FDA UNII
19BN8D5HET
Created by admin on Sat Dec 16 10:24:42 GMT 2023 , Edited by admin on Sat Dec 16 10:24:42 GMT 2023
PRIMARY
PUBCHEM
190536
Created by admin on Sat Dec 16 10:24:42 GMT 2023 , Edited by admin on Sat Dec 16 10:24:42 GMT 2023
PRIMARY
CAS
76596-58-2
Created by admin on Sat Dec 16 10:24:42 GMT 2023 , Edited by admin on Sat Dec 16 10:24:42 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE