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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H9N3O2S2
Molecular Weight 255.317
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFATHIAZOLE

SMILES

NC1=CC=C(C=C1)S(=O)(=O)NC2=NC=CS2

InChI

InChIKey=JNMRHUJNCSQMMB-UHFFFAOYSA-N
InChI=1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
SULFATHIAZOLE
EP   GREEN BOOK   HSDB   INN   MART.   MI   USP   USP-RS   VANDF   WHO-DD  
INN  
Official Name English
SULFATHIAZOLE [VANDF]
Common Name English
SULFATHIAZOLE [ORANGE BOOK]
Common Name English
SULFATHIAZOLE [EP MONOGRAPH]
Common Name English
SULFATHIAZOLE [GREEN BOOK]
Common Name English
Sulfathiazole [WHO-DD]
Common Name English
TRIPLE SULFA (SULFATHIAZOLE)
Common Name English
SULPHATHIAZOLE
Common Name English
SULFATHIAZOLE COMPONENT OF TRYSUL
Common Name English
TRIPLE SULFA (SULFATHIAZOLE) [ORANGE BOOK]
Common Name English
N(SUP 1)-2-THIAZOLYLSULFANILAMIDE
Systematic Name English
VAGILIA COMPONENT SULFATHIAZOLE
Common Name English
SULFATHIAZOLE [USP MONOGRAPH]
Common Name English
SULFATHIAZOLE COMPONENT OF SULTRIN
Common Name English
TRYSUL COMPONENT SULFATHIAZOLE
Common Name English
SULFATHIAZOLE [HSDB]
Common Name English
SULFATHIAZOLE COMPONENT OF GYNE-SULF
Common Name English
NSC-683531
Code English
SULTRIN COMPONENT SULFATHIAZOLE
Common Name English
SULFATHIAZOLE [MART.]
Common Name English
sulfathiazole [INN]
Common Name English
GYNE-SULF COMPONENT SULFATHIAZOLE
Common Name English
BENZENESULFONAMIDE, 4-AMINO-N-2-THIAZOLYL-
Systematic Name English
SULFATHIAZOLE [MI]
Common Name English
NSC-31812
Code English
SULFATHIAZOLE [USP-RS]
Common Name English
SULFATHIAZOLE COMPONENT OF VAGILIA
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 77903
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
WHO-VATC QJ01EQ07
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
WHO-ATC J01EB07
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
WHO-VATC QD06BA02
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
WHO-ATC D06BA02
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
Code System Code Type Description
SMS_ID
100000083763
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
RS_ITEM_NUM
1636504
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
NSC
31812
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
CAS
6052-33-1
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
SUPERSEDED
NCI_THESAURUS
C66571
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
CAS
859037-27-7
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
SUPERSEDED
CAS
158269-46-6
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
SUPERSEDED
INN
428
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
MERCK INDEX
m10344
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY Merck Index
RXCUI
10193
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY RxNorm
FDA UNII
Y7FKS2XWQH
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
EPA CompTox
DTXSID8026068
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
HSDB
4380
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
DRUG CENTRAL
2527
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-771-5
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
DRUG BANK
DB06147
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
DAILYMED
Y7FKS2XWQH
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
WIKIPEDIA
SULFATHIAZOLE
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
EVMPD
SUB10731MIG
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
PUBCHEM
5340
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
NSC
683531
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
ChEMBL
CHEMBL437
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
MESH
C005312
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
CHEBI
9337
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
CAS
72-14-0
Created by admin on Fri Dec 15 15:01:46 UTC 2023 , Edited by admin on Fri Dec 15 15:01:46 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of SULFATHIAZOLE
SALT/SOLVATE (PARENT)
Structure of SULFATHIAZOLE SILVER
SALT/SOLVATE (PARENT)
Structure of PHENYLEPHRINE SULFATHIAZOLE
SALT/SOLVATE (PARENT)
Structure of SULFATHIAZOLE ZINC
SALT/SOLVATE (PARENT)
Structure of SULFATHIAZOLE SODIUM
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966