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

Details

Stereochemistry ACHIRAL
Molecular Formula C13H13N3O3S
Molecular Weight 291.326
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMIDAPSONE

SMILES

NC(=O)NC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(N)C=C2

InChI

InChIKey=UPWPBIUUSLIWAI-UHFFFAOYSA-N
InChI=1S/C13H13N3O3S/c14-9-1-5-11(6-2-9)20(18,19)12-7-3-10(4-8-12)16-13(15)17/h1-8H,14H2,(H3,15,16,17)

HIDE SMILES / InChI
Amidapsone (aminoureidosulfone) is an urea analog of dapsone used in treatment of herpesvirus caused Marek's diseases.

Approval Year

PubMed

PubMed

TitleDatePubMed
AUS in the prevention of Marek's disease.
1984-01-01
Evaluation of the sulfones and streptomycin in experimental tuberculosis.
1949-12-14
Patents

Sample Use Guides

Chicks infected with Marek's disease (MD) virus (5000 plaque-forming units) at 1 day of age were given Amidapsone in the feed from 1 day of age until the experiment was terminated. Amidapsone, at all concentrations tested, reduced mortality due to Marek's disease. Chickens receiving Amidapsone at the 0.002% level had a 4% mortality rate, those receiving 0.005% had 9% mortality, and those receiving 0.01% had 2% mortality; mortality rates in the respective controls were 44%, 49%, and 50%.
Route of Administration: Oral
Name Type Language
AMIDAPSONE
INN   USAN  
INN   USAN  
Official Name English
SULFACIDE
Preferred Name English
NSC-28120
Code English
(P-SULFANILYLPHENYL)UREA
Common Name English
AMIDAPSONE [USAN]
Common Name English
amidapsone [INN]
Common Name English
UREA, (4-((4-AMINOPHENYL)SULFONYL)PHENYL)-
Systematic Name English
UREA, N-(4-((4-AMINOPHENYL)SULFONYL)PHENYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C849
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
Code System Code Type Description
INN
3290
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID80189201
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
NSC
28120
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
SMS_ID
100000087221
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
EVMPD
SUB05426MIG
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
CAS
3569-77-5
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
FDA UNII
8N5BE1I42E
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105929
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
PUBCHEM
66267
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY
NCI_THESAURUS
C73196
Created by admin on Mon Mar 31 18:31:46 GMT 2025 , Edited by admin on Mon Mar 31 18:31:46 GMT 2025
PRIMARY