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Details

Stereochemistry ACHIRAL
Molecular Formula C9H10N4O2S2
Molecular Weight 270.331
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFAMETHIZOLE

SMILES

CC1=NN=C(NS(=O)(=O)C2=CC=C(N)C=C2)S1

InChI

InChIKey=VACCAVUAMIDAGB-UHFFFAOYSA-N
InChI=1S/C9H10N4O2S2/c1-6-11-12-9(16-6)13-17(14,15)8-4-2-7(10)3-5-8/h2-5H,10H2,1H3,(H,12,13)

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
SULFAMETHIZOLE
EP   GREEN BOOK   HSDB   INN   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD  
INN  
Official Name English
NSC-757327
Code English
SULFAMETHIZOLE [ORANGE BOOK]
Common Name English
SULPHAMETHIZOLE
Common Name English
SULFAMETHIZOLE [EP IMPURITY]
Common Name English
N (SUP 1)-(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANILAMIDE
Systematic Name English
sulfamethizole [INN]
Common Name English
SULFAMETHIZOLE [MART.]
Common Name English
SULFAMETHIZOLE [VANDF]
Common Name English
BENZENESULFONAMIDE, 4-AMINO-N-(5-METHYL-1,3,4-THIADIAZOL-2-YL)-
Systematic Name English
SULFAMETHIZOLE [MI]
Common Name English
SULFAMETHIZOLE [EP MONOGRAPH]
Common Name English
SULFAMETHIZOLE [HSDB]
Common Name English
SULFAMETHIZOLE [JAN]
Common Name English
SULFAMETHIZOLE [USP MONOGRAPH]
Common Name English
THIOSULFIL
Brand Name English
Sulfamethizole [WHO-DD]
Common Name English
SULFAMETHIZOLE [USP-RS]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 520.2280
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-VATC QD06BA04
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-ATC B05CA04
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-ATC S01AB01
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-VATC QB05CA04
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-ATC D06BA04
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-VATC QS01AB01
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
LIVERTOX 910
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
NCI_THESAURUS C29739
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-VATC QJ01EQ02
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
WHO-ATC J01EB02
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL1191
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
CAS
144-82-1
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
INN
529
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
NSC
757327
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
MESH
D013419
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
EVMPD
SUB10710MIG
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
SMS_ID
100000092325
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
RS_ITEM_NUM
1630009
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
CHEBI
9331
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
DRUG BANK
DB00576
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
ECHA (EC/EINECS)
205-641-1
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
HSDB
4379
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
RXCUI
10179
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID5023615
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
WIKIPEDIA
SULFAMETHIZOLE
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
FDA UNII
25W8454H16
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
MERCK INDEX
m10318
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY Merck Index
DAILYMED
25W8454H16
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
PUBCHEM
5328
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
NCI_THESAURUS
C47736
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
DRUG CENTRAL
2512
Created by admin on Fri Dec 15 15:01:54 UTC 2023 , Edited by admin on Fri Dec 15 15:01:54 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of SULFAMETHIZOLE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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