U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C9H5Br2NO
Molecular Weight 302.95
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROXYQUINOLINE

SMILES

OC1=C2N=CC=CC2=C(Br)C=C1Br

InChI

InChIKey=ZDASUJMDVPTNTF-UHFFFAOYSA-N
InChI=1S/C9H5Br2NO/c10-6-4-7(11)9(13)8-5(6)2-1-3-12-8/h1-4,13H

HIDE SMILES / InChI

Molecular Formula C9H5Br2NO
Molecular Weight 302.95
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Broxyquinoline is an anti-infective agent. It exerts activity against fungi and protozoa. Broxyquinoline (Intestopan) has been used in the treatment of diarrhoeas of different aetiology. Broxyquinoline is able to promote neovascularization.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: UNIPROT: Q208C2 (Acyl-CoA-binding protein)
64.9 µM [IC50]
PubMed

PubMed

TitleDatePubMed
2-[(5,7-Dibromo-quinolin-8-yl)-oxy]-N-(2-meth-oxy-phen-yl)acetamide.
2010-11-24
Liquid phase microextraction and ultratrace determination of cadmium by modified graphite furnace atomic absorption spectrometry.
2009-06-15
Solid phase extraction vis-à-vis coprecipitation preconcentration of cadmium and lead from soils onto 5,7-dibromoquinoline-8-ol embedded benzophenone and determination by FAAS.
2006-06-15
The evaluation of liposome-water partitioning of 8-hydroxyquinolines and their copper complexes.
2006-03-15
A simple spectrophotometric method for the determination of cadmium in industrial, environmental, biological and soil samples using 5,7-dibromo-8-hydroxyquinoline.
2004-06
A rapid spectrophotometric method for the determination of molybdenum in industrial, environmental, biological and soil samples using 5,7-dibromo-8-hydroxyquinoline.
2002-04
A study on the neurotoxicity of broxyquinoline and brobenzoxaldine combination in therapeutic doses.
1986-01
THE IN VITRO EFFECT OF 8-HYDROXYQUINOLINE DERIVATIVES ON STRAINS OF MYCOBACTERIUM TUBERCULOSIS.
1964-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:29:47 GMT 2025
Edited
by admin
on Mon Mar 31 18:29:47 GMT 2025
Record UNII
UK4C618C8T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STAROGYN
Preferred Name English
BROXYQUINOLINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
BROXYQUINOLINE [MI]
Common Name English
5,7-DIBROMO-8-QUINOLINOL
Systematic Name English
NSC-1810
Code English
Broxyquinoline [WHO-DD]
Common Name English
DIBROMOXIN
Systematic Name English
broxyquinoline [INN]
Common Name English
BROXYQUINOLINE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
WHO-ATC P01AA01
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
WHO-VATC QA07AX01
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
WHO-ATC G01AC06
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
WHO-VATC QG01AC06
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
WHO-ATC A07AX01
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID9045849
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
FDA UNII
UK4C618C8T
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
DRUG BANK
DB13536
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
WIKIPEDIA
BROXYQUINOLINE
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
MESH
C002276
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
INN
1244
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
EVMPD
SUB05940MIG
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
PUBCHEM
2453
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
SMS_ID
100000085842
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
CAS
521-74-4
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
NCI_THESAURUS
C73253
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
MERCK INDEX
m2732
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY Merck Index
DRUG CENTRAL
412
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-317-8
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
ChEMBL
CHEMBL223448
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
NSC
1810
Created by admin on Mon Mar 31 18:29:47 GMT 2025 , Edited by admin on Mon Mar 31 18:29:47 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY