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Details

Stereochemistry ACHIRAL
Molecular Formula C13H11N3O5S
Molecular Weight 321.309
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of SALAZOSULFAMIDE

SMILES

NS(=O)(=O)C1=CC=C(C=C1)\N=N\C2=CC(C(O)=O)=C(O)C=C2

InChI

InChIKey=NBSRUZQXRUNPNY-FOCLMDBBSA-N
InChI=1S/C13H11N3O5S/c14-22(20,21)10-4-1-8(2-5-10)15-16-9-3-6-12(17)11(7-9)13(18)19/h1-7,17H,(H,18,19)(H2,14,20,21)/b16-15+

HIDE SMILES / InChI

Molecular Formula C13H11N3O5S
Molecular Weight 321.309
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Salazosulfamide was studied for the treatment of ankylosing spondylitis. It was found that salazosulfamide efficacy is associated with N-acetyltransferase 1 polymorphisms and in particularly, NAT1 AA/GG genotype at 263 locus. However, future studies should be conducted to investigate these issues.

Approval Year

PubMed

PubMed

TitleDatePubMed
Efficacy research of salazosulfamide in ankylosing spondylitis and NAT1 gene polymorphism.
2017-10
NAT2 polymorphisms combining with smoking associated with breast cancer susceptibility: a meta-analysis.
2010-10
[Observation on therapeutic effect of heat needle combined with herb iontophoresis and western medicine on rheumatoid arthritis].
2007-10
Enhancement of reductive metabolism of p-nitrobenzoate and nitrazepam in isolated perfused rat liver by ethanol.
1979-05-01

Sample Use Guides

The experimental group received 7.5 mg of salazosulfamide (MTX) per week
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:15:48 GMT 2025
Edited
by admin
on Mon Mar 31 18:15:48 GMT 2025
Record UNII
B6831ORH7W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-27236
Preferred Name English
SALAZOSULFAMIDE
INN  
INN  
Official Name English
salazosulfamide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29739
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
Code System Code Type Description
SMS_ID
100000080523
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
INN
2212
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID801317062
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
NCI_THESAURUS
C72640
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
CAS
139-56-0
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
NSC
27236
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
EVMPD
SUB10420MIG
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
ChEMBL
CHEMBL377353
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
FDA UNII
B6831ORH7W
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-366-7
Created by admin on Mon Mar 31 18:15:48 GMT 2025 , Edited by admin on Mon Mar 31 18:15:48 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY