N-Acetyl dapsone

CAS : 565-20-8

Ref. 3D-FA17014

Informations sur le produit

• Nom: N-Acetyl dapsone
• Synonymes: N-[4-[(4-Aminophenyl)sulfonyl]phenyl]-acetamide4-Acetamido-4'-aminodiphenyl sulphoneMADDS, 4'-Sulfanilylacetanilide, 4-Acetamido-4′-aminodiphenyl sulfone, 4-Acetamidophenyl 4′-aminophenyl sulfone, 4-Acetylamino-4′-aminodiphenyl sulfone, 4-Acetylamino-4′-aminophenyl sulfone, 4-Amino-4′-acetamidodiphenyl sulfone, Acetamide, N-(4-((4-aminophenyl)sulfonyl)phenyl)-, Acetamide, N-(4-((4-aminophenyl)sulfonyl)phenyl)- (9CI), Acetanilide, 4'-sulfanilyl-, Acetyldapsone, Brn 2746651, Ccris 5693, Madds, Monoacetyldapsone, N-(4-((4-Aminophenyl)sulfonyl)phenyl)acetamide, N-Acetyl-4,4'-diaminodiphenylsulfone, N-Acetyldapsone, Nsc 27184
• CAS: 565-20-8

Description

N-Acetyl dapsone is a drug used to treat metabolic disorders. It is a structural analog of dapsone that has the same mechanism of action and therapeutic use, but with fewer side effects. N-Acetyl dapsone is converted by oxidation in the liver to dapsone, which inhibits the activity of a number of enzymes, including dehydrogenases and monoamine oxidases. The activity index for N-acetyl dapsone is 1.5 times that for dapsone. The binding constants for N-acetyl dapsone are higher than those for dapsone and have been shown to be more selective for human serum albumin than for rat liver microsomes. In addition, N-acetyl dapsone does not bind to lysine residues on proteins as well as does its parent compound, which may explain its lower incidence of side effects such as agranulocytosis and methemoglobinemia in humans compared

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 290.34 g/mol
• Formule: C₁₄H₁₄N₂O₃S
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: 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)
• Code InChI: InChIKey=WDOCBIHNYYQINH-UHFFFAOYSA-N
• SMILES: CC(=O)Nc1ccc(S(=O)(=O)c2ccc(N)cc2)cc1