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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10Br2ClNO2S
Molecular Weight 463.571
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BROTIANIDE

SMILES

CC(=O)OC1=C(Br)C=C(Cl)C=C1C(=S)NC2=CC=C(Br)C=C2

InChI

InChIKey=NRFGEDASJHBPPN-UHFFFAOYSA-N
InChI=1S/C15H10Br2ClNO2S/c1-8(20)21-14-12(6-10(18)7-13(14)17)15(22)19-11-4-2-9(16)3-5-11/h2-7H,1H3,(H,19,22)

HIDE SMILES / InChI

Molecular Formula C15H10Br2ClNO2S
Molecular Weight 463.571
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

BROTIANIDE is salicylanilide derivative used to treat fascioliasis in sheep. A dose of 7 mg/kg of brotianide shows 91-99% activity against 7-14 weeks old flukes; however, its activity against 6 weeks old flukes is weak (50-90%). It also possesses 85-90% activity against paramphistomes in sheep and cattle. The maximum tolerated dose of brotianide is 27 mg/kg in sheep.

Approval Year

PubMed

PubMed

TitleDatePubMed
Treatment of Dicrocoelium dendriticum with a combination of thiophanate and brotianide.
1988 Dec 17
Patents

Patents

Sample Use Guides

A dose of 7 mg/kg of brotianide shows 91-99% activity against 7-14 weeks old flukes; The maximum tolerated dose of brotianide is 27 mg/kg in sheep
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:59:56 GMT 2023
Edited
by admin
on Fri Dec 15 15:59:56 GMT 2023
Record UNII
30OGU6XH7S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BROTIANIDE
INN   MART.  
INN  
Official Name English
3,4'DIBROMO-5-CHLOROTHIOSALICYLANILIDE ACETATE (ESTER)
Common Name English
brotianide [INN]
Common Name English
FBA-4059
Code English
BROTIANIDE [MART.]
Common Name English
BAY 4059 VA
Code English
FBA 4059
Code English
BAY-4059-VA
Code English
Classification Tree Code System Code
NCI_THESAURUS C250
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
Code System Code Type Description
EVMPD
SUB05932MIG
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
FDA UNII
30OGU6XH7S
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
MESH
C010873
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID00177807
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106593
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
ECHA (EC/EINECS)
245-505-9
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
CAS
23233-88-7
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
PUBCHEM
3034337
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
INN
2904
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
SMS_ID
100000085838
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
NCI_THESAURUS
C72595
Created by admin on Fri Dec 15 15:59:56 GMT 2023 , Edited by admin on Fri Dec 15 15:59:56 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY