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

Details

Stereochemistry ACHIRAL
Molecular Formula C12H12N2O2S
Molecular Weight 248.301
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFABENZ

SMILES

NC1=CC=C(C=C1)S(=O)(=O)NC2=CC=CC=C2

InChI

InChIKey=YBUXKQSCKVQATK-UHFFFAOYSA-N
InChI=1S/C12H12N2O2S/c13-10-6-8-12(9-7-10)17(15,16)14-11-4-2-1-3-5-11/h1-9,14H,13H2

HIDE SMILES / InChI

Molecular Formula C12H12N2O2S
Molecular Weight 248.301
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfabenz is an antibacterial; coccidiostat (for poultry).

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Identification of a class of sulfonamides highly active against dihydropteroate synthase form Toxoplasma gondii, Pneumocystis carinii, and Mycobacterium avium.
1996-03
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:46:35 GMT 2025
Edited
by admin
on Mon Mar 31 17:46:35 GMT 2025
Record UNII
2Y70F6K03F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFABENZ
INN   MI   USAN  
USAN   INN  
Official Name English
NSC-2619
Preferred Name English
SULFABENZ [USAN]
Common Name English
4-AMINO-N-PHENYLBENZENESULFONAMIDE
Systematic Name English
SULFABENZ [MI]
Common Name English
sulfabenz [INN]
Common Name English
Sulfanilanilide
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29739
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
Code System Code Type Description
CAS
127-77-5
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
FDA UNII
2Y70F6K03F
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
SMS_ID
100000083259
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-865-7
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
NCI_THESAURUS
C152452
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
ChEMBL
CHEMBL359839
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
NSC
2619
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
INN
2227
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID9046287
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
PUBCHEM
31390
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
MERCK INDEX
m10298
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY Merck Index
EVMPD
SUB10683MIG
Created by admin on Mon Mar 31 17:46:35 GMT 2025 , Edited by admin on Mon Mar 31 17:46:35 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY