Sulfathiazole

CAS : 72-14-0

Ref. 3D-FS27944

Informations sur le produit

• Nom: Sulfathiazole
• Synonymes: 4-Amino-N-2-thiazolylbenzenesulfonamide, 2-(P-Aminobenzenesulfonamido)Thiazole, 2-(Sulfanilylamino)thiazole, 2-(p-Aminobenzenesulphonamido)thiazole, 2-Sulfanilamidothiazole, 2-Sulfathiazole, 2090 R.P., 4-Amino-N-2-Thiazolyl-Benzenesulfonamide, 4-Amino-N-2-thiazolylbenzensulfonamide, 4-[(1,3-Thiazol-2-yl)aminosulfonyl]aniline, 4-amino-N-(1,3-thiazol-2-yl)benzenesulfonamide, Azoquimiol, Azoseptale, Benzenesulfonamide, 4-amino-N-2-thiazolyl-, Chemosept, Ciba 3714, Cibazol, Duatok, Dulana, Eleudron, Enterobiocine, Estafilol, M and B 760, M&B 760, N'-2-thiazolylsulfanylamide, N-(Thiazol-2-yl)-4-aminobenzenesulfonamide, N1-(2-Thiazolyl)sulfanilamide, N¹-(2-Thiazolyl)sulfanilamide, Neostrepsan, Norsulfasol, Norsulfazol, Norsulfazole, Nsc 31812, Nsc 683531, Planomide, Poliseptil, ST, Sanotiazol, Streptosilthiazole, Sulfamul, Sulfanilamide, N1-2-thiazolyl-, Sulfanilamide, N1-4-thiazolin-2-ylidene-, Sulfanilamide, N¹-2-thiazolyl-, Sulfanilamide, N¹-4-thiazolin-2-ylidene-, Sulfanilamidothiazole, Sulfanilamine, N1-2-Thiazolyl-, Sulfathiazol, Sulfathiazole Granule, Sulfatiazol, Sulfavitina, Sulfocerol, Sulphathiazole, Sulzol, Thiacoccine, Thiasulfol, Thiazamide, Thiozamide, Wintrazole, p-Amino-N-(2-thiazolyl)benzenesulfonamide
• CAS: 72-14-0

Description

Sulfathiazole is a sulfonamide antibacterial agent with a chemical structure similar to that of the sulfa drugs. It is active against Gram-positive and Gram-negative bacteria, including those resistant to other antibiotics. Sulfathiazole has been shown to be effective against infectious diseases caused by Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, and Salmonella typhi. The mechanism of action of sulfathiazole is not fully understood. One hypothesis is that it inhibits the synthesis of folic acid in bacteria by inhibiting enzymes involved in purine metabolism. This drug also has complex pharmacological effects on human cells because it can inhibit both receptor activity and enzyme activity in complex cellular processes such as protein synthesis and DNA synthesis.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 255.32 g/mol
• Formule: C₉H₉N₃O₂S₂
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)
• Code InChI: InChIKey=JNMRHUJNCSQMMB-UHFFFAOYSA-N
• SMILES: Nc1ccc(S(=O)(=O)Nc2nccs2)cc1