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Details

Stereochemistry ACHIRAL
Molecular Formula C24H28Br2N2O4.ClH
Molecular Weight 604.759
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROVANEXINE HYDROCHLORIDE

SMILES

Cl.COC1=CC(=CC=C1OC(C)=O)C(=O)NC2=C(CN(C)C3CCCCC3)C=C(Br)C=C2Br

InChI

InChIKey=GOPILTWRTSSNPV-UHFFFAOYSA-N
InChI=1S/C24H28Br2N2O4.ClH/c1-15(29)32-21-10-9-16(12-22(21)31-3)24(30)27-23-17(11-18(25)13-20(23)26)14-28(2)19-7-5-4-6-8-19;/h9-13,19H,4-8,14H2,1-3H3,(H,27,30);1H

HIDE SMILES / InChI

Molecular Formula C24H28Br2N2O4
Molecular Weight 568.298
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Brovanexine is a derivative of bromhexine used as an adjunct to antibacterials in preparations for the treatment of respiratory-tract infections. Oral administration of brovanexine hydrochloride (BR-222) caused a significant increase in the output volume of respiratory tract fluid. Brovanexine at 10 and 20 mg/kg showed a tendency to reduce the viscosity of respiratory tract fluid in anesthetized dogs. Brovanexine also showed a tendency to reduce the viscosity of sputum obtained from the SO2-exposed rabbits.

Approval Year

PubMed

PubMed

TitleDatePubMed
Molecular nature of three liver alkaline phosphatases detected by drug administration in vivo: differences between soluble and membranous enzymes.
1987
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Sources: Archivos de Farmacologia y Toxicologia Volume 2 Issue 1 Pages 61-8 Journal 1976
Brovanexine (50 mg​/kg, orally) increased secretion of nasal mucus in rabbits.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:53:18 GMT 2023
Edited
by admin
on Fri Dec 15 16:53:18 GMT 2023
Record UNII
51I4IS0SMG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BROVANEXINE HYDROCHLORIDE
MART.   WHO-DD  
Common Name English
BR-222
Code English
4-(ACETYLOXY)-N-(2,4-DIBROMO-6-((CYCLOHEXYLMETHYLAMINO)METHYL)PHENYL)-3-METHOXYBENZAMIDE MONOHYDROCHLORIDE
Systematic Name English
UR-389
Code English
BR 222
Code English
BROVANEXINE HCL
Common Name English
Brovanexine hydrochloride [WHO-DD]
Common Name English
BROVANEXINE HYDROCHLORIDE [MART.]
Common Name English
BENZAMIDE, 4-(ACETYLOXY)-N-(2,4-DIBROMO-6-((CYCLOHEXYLMETHYLAMINO)METHYL)PHENYL)-3-METHOXY-, HYDROCHLORIDE (1:1)
Systematic Name English
UR 389
Code English
Classification Tree Code System Code
NCI_THESAURUS C74536
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C95604
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
SMS_ID
100000085125
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID90202718
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
CAS
54340-60-2
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
DRUG BANK
DBSALT002815
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
RXCUI
402579
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY RxNorm
EVMPD
SUB00882MIG
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
FDA UNII
51I4IS0SMG
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
259-110-4
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
PUBCHEM
20055430
Created by admin on Fri Dec 15 16:53:18 GMT 2023 , Edited by admin on Fri Dec 15 16:53:18 GMT 2023
PRIMARY
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ACTIVE MOIETY