Sulphanilamide

CAS : 63-74-1

Ref. 3D-FS07881

Informations sur le produit

• Nom: Sulphanilamide
• Synonymes: p-Aminobenzenesulfonamide, (4-(Aminosulfonyl)phenyl)amine, 1162F, 4-(Aminosulfonyl)aniline, 4-Aminobenzene-1-sulfonamide, 4-Aminobenzenesulfonamide, 4-Aminophenylsulfonamide, 4-Aminosulfoneamide, 4-Sulfamoylaniline, A-349, AVC, Albexan, Albosal, Ambeside, Aminobenzenesulfonamide, Antistrept, Astreptine, Astrocid, Bacteramid, Bactesid, Collomide, Colsulanyde, Copticide, Deseptyl, Dipron, Ergaseptine, Erysipan, Estreptocida, Exoseptoplix, Gerison, Gombardol, Infepan, Lusil, Lysococcine, Neococcyl, Orgaseptine, P-Aminophenylsulfonamide, Pabs, Prontalbin, Prontylin, Proseptal, Proseptine, Proseptol, Pysococcine, Sanamid, Septanilam, Septinal, Septolix, Septoplex, Septoplix, Stramid, Strepamide, Strepsan, Streptagol, Streptamid, Streptasol, Streptocid, Streptocide, Streptoclase, Streptocom, Streptol, Strepton, Streptopan, Streptosil, Streptozol, Streptozone, Streptrocide, Sulfamidyl, Sulfamine, Sulfana, Sulfanalone, Sulfanidyl, Sulfanil, Sulfanilamid, Sulfanilamida, Sulfanilimide, Sulfocidine, Sulfonamid, Sulfonamide, Sulfonylamide, Sulphonamide, Therapol, Tolder, Vagitrol, p-Anilinesulfonamide, p-Sulfamidoaniline, p-Sulfamoylaniline, sulfonamide p, prontosil albom, aniline-p-sulfonic amide, pronzin album, rubiazol a, septamide album, fourneau 1162, Industrial Sulfanilamide, Sulphanilamide crystals, prontosil white, stopton album, Streptocid album, Prontosil album, Sulfanilamide, prontosil i, 1162 F, F 1162, F 1162, Benzenesulfonamide, 4-amino-

Description

Sulphanilamide is an antimicrobial agent that inhibits the growth of bacteria by binding to their enzymes and blocking protein synthesis. In addition, sulphanilamide has been shown to inhibit the production of sulfanilamide, a potent inhibitor of tetracycline. Sulphanilamide is soluble in water and alcohol but not in organic solvents. The solubility of sulphanilamide can be increased by adding sodium salts or pH adjustment. Sulphanilamide is also used for wastewater treatment as it has inhibitory properties against sulfate-reducing bacteria. X-ray crystal structures have revealed that sulphanilamide binds to the active site of bacterial beta-lactamases through hydrogen bonds with both the NH group and the COOH group on its sulfur atom, resulting in inhibition of these enzymes. Sulphanilamide also interferes with bacterial DNA replication by inhibiting dna gyrase and topoisomerase IV. Sulphanilamide also

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 172.21 g/mol
• Formule: C₆H₈N₂O₂S
• Couleur/Forme: Powder
• InChI: InChI=1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)
• Code InChI: InChIKey=FDDDEECHVMSUSB-UHFFFAOYSA-N
• SMILES: Nc1ccc(S(N)(=O)=O)cc1