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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14N2O3S
Molecular Weight 290.338
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOACETYLDAPSONE

SMILES

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

InChI

InChIKey=WDOCBIHNYYQINH-UHFFFAOYSA-N
InChI=1S/C14H14N2O3S/c1-10(17)16-12-4-8-14(9-5-12)20(18,19)13-6-2-11(15)3-7-13/h2-9H,15H2,1H3,(H,16,17)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Interaction of sulfonamide and sulfone compounds with Toxoplasma gondii dihydropteroate synthase.
1990-02
Bilirubin/rat serum albumin interaction.
1986
Binding of dapsone and its analogues to human serum albumin.
1985-06
Bilirubin-displacing effect of ampicillin, indomethacin, chlorpromazine, gentamicin, and parabens in vitro and in newborn infants.
1983-03
Name Type Language
NSC-27184
Preferred Name English
MONOACETYLDAPSONE
Common Name English
ACETAMIDE, N-(4-((4-AMINOPHENYL)SULFONYL)PHENYL)-
Systematic Name English
4'-SULFANILYLACETANILIDE
Systematic Name English
Code System Code Type Description
NSC
27184
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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FDA UNII
A4YKS8ULCN
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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CAS
565-20-8
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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MESH
C018965
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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CHEBI
139473
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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PUBCHEM
11257
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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EPA CompTox
DTXSID70205040
Created by admin on Mon Mar 31 19:04:38 GMT 2025 , Edited by admin on Mon Mar 31 19:04:38 GMT 2025
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