CAS 72-14-0
:Sulfatiazol
- 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-thiazolylbenzenesulfonamide
- 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
- N<sup>1</sup>-(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, N<sup>1</sup>-2-thiazolyl-
- Sulfanilamide, N<sup>1</sup>-4-thiazolin-2-ylidene-
- Sulfanilamidothiazole
- Sulfanilamine, N1-2-Thiazolyl-
- Sulfathiazol
- Sulfathiazole
- Sulfathiazole Granule
- Sulfatiazol
- Sulfavitina
- Sulfocerol
- Sulphathiazole
- Sulzol
- Thiacoccine
- Thiasulfol
- Thiazamide
- Thiozamide
- Wintrazole
- Ver más sinónimos
Sulfathiazole
CAS:Producto controladoApplications Antibacterial.This compound is a contaminant of emerging concern (CECs).
References Kapoor, V.K., et al.: Anal. Profiles Drug Subs. Excip., 22, 389 (1993),Fórmula:C9H9N3O2S2Forma y color:NeatPeso molecular:255.324-Amino-N-(thiazol-2-yl)benzenesulfonamide
CAS:Fórmula:C9H9N3O2S2Pureza:95%Forma y color:Solid, Crystalline Powder or PowderPeso molecular:255.31Sulfathiazole
CAS:4-Amino-N-(thiazol-2-yl)benzenesulfonamideFórmula:C9H9N3O2S2Pureza:98+%Peso molecular:255.32Sulfathiazole
CAS: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.
Fórmula:C9H9N3O2S2Pureza:Min. 95%Forma y color:PowderPeso molecular:255.32 g/mol





