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Details

Stereochemistry RACEMIC
Molecular Formula C9H15BrN2O2
Molecular Weight 263.132
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROXATEROL

SMILES

CC(C)(C)NCC(O)C1=CC(Br)=NO1

InChI

InChIKey=JBRBWHCVRGURBA-UHFFFAOYSA-N
InChI=1S/C9H15BrN2O2/c1-9(2,3)11-5-6(13)7-4-8(10)12-14-7/h4,6,11,13H,5H2,1-3H3

HIDE SMILES / InChI

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
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 16:59:55 UTC 2023
Edited
by admin
on Sat Dec 16 16:59:55 UTC 2023
Record UNII
ZE4IRB4DUC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BROXATEROL
INN   MART.  
INN  
Official Name English
BROXATEROL [MART.]
Common Name English
broxaterol [INN]
Common Name English
(±)-3-BROMO-.ALPHA.-((TERT-BUTYLAMINO)METHYL)-5-ISOXAZOLEMETHANOL
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
Code System Code Type Description
EVMPD
SUB05937MIG
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
MESH
C045916
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
PUBCHEM
71149
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
SMS_ID
100000085860
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID20868402
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
CAS
76596-57-1
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
WIKIPEDIA
BROXATEROL
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
INN
5481
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
NCI_THESAURUS
C74195
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
ChEMBL
CHEMBL2105475
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
ECHA (EC/EINECS)
278-494-4
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
FDA UNII
ZE4IRB4DUC
Created by admin on Sat Dec 16 16:59:56 UTC 2023 , Edited by admin on Sat Dec 16 16:59:56 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY