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Details

Stereochemistry ACHIRAL
Molecular Formula C11H13N3O3S
Molecular Weight 267.304
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFATROXAZOLE

SMILES

CC1=C(C)C(NS(=O)(=O)C2=CC=C(N)C=C2)=NO1

InChI

InChIKey=DAUFGBIKKGOPJA-UHFFFAOYSA-N
InChI=1S/C11H13N3O3S/c1-7-8(2)17-13-11(7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6H,12H2,1-2H3,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C11H13N3O3S
Molecular Weight 267.304
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfatroxazole is a sulfamide derivative patented by Swiss multinational healthcare company F. Hoffmann-La Roche & Co., A.-G. as an antibacterial agent and bacteriostatic antibiotic. Sulfatroxazole competitively inhibits dihydropteroate synthase preventing the formation of dihydropteroic acid, a precursor of folic acid which is required for bacterial growth. Sulfatroxazole is a component present in various veterinary drugs.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
260.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Pharmacokinetics, metabolism and renal excretion of sulfatroxazole and its 5-hydroxy- and N4-acetyl-metabolites in man.
1986 May-Jun
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:15:13 GMT 2023
Edited
by admin
on Fri Dec 15 19:15:13 GMT 2023
Record UNII
ZXC0PT8FFS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFATROXAZOLE
INN   MART.  
INN  
Official Name English
sulfatroxazole [INN]
Common Name English
N(SUP 1)-(4,5-DIMETHYL-3-ISOXAZOLYL)SULFANILAMIDE
Systematic Name English
SULFATROXAZOLE [MART.]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01EW14
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
WHO-VATC QJ01EQ14
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
Code System Code Type Description
INN
3362
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
ChEMBL
CHEMBL26630
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
SMS_ID
100000083784
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
MESH
C048358
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
EPA CompTox
DTXSID20177829
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
NCI_THESAURUS
C152459
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
EVMPD
SUB10734MIG
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
FDA UNII
ZXC0PT8FFS
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
PUBCHEM
31771
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
CAS
23256-23-7
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
ECHA (EC/EINECS)
245-530-5
Created by admin on Fri Dec 15 19:15:13 GMT 2023 , Edited by admin on Fri Dec 15 19:15:13 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY