| Identification | More | [Name]
Sulfathiazole sodium | [CAS]
144-74-1 | [Synonyms]
4-AMINO-N-2-THIAZOLYBENZENESULFONAMIDE SODIUM SALT
4-AMINO-N-(2-THIAZOLYL)BENZENESULFONAMIDE SODIUM SALT
LABOTEST-BB LT00772308
SODIUM SULFATHIAZOLE
SULFATHIAZOLE
SULFATHIAZOLE SODIUM
SULFATHIAZOLE SODIUM SALT
thiazamide
(n(sup1)-2-thiazolylsulfanilamido)-sodiu
2-sulfanilamidothiazolesodiumsalt
4-amino-n-2-thiazolyl-benzenesulfonamidmonosodiumsalt
monosodium2-sulfanilamidothiazole
n(sup1)-2-thiazolylsulfanilamidesodiumsalt
n(sup1)-2-thiazolyl-sulfanilamidmonosodiumsalt
n(sup1)-2-thiazolyl-sulfanilamidn(sup1)-sodiumderiv.
sodium2-sulfanilamidothiazole
sodiumnorsulfazole
sodiumsulphathiazole
solublesulfathiazole
ST-NA | [EINECS(EC#)]
205-638-5 | [Molecular Formula]
C9H9N3NaO2S2 | [MDL Number]
MFCD00072133 | [Molecular Weight]
278.31 | [MOL File]
144-74-1.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S24/25:Avoid contact with skin and eyes .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) . | [WGK Germany ]
2
| [RTECS ]
WP2450000
| [F ]
10 |
| Hazard Information | Back Directory | [Uses]
Sulfathiazole sodium salt is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA). It can also be used in biological study of thermotherapy and sulfonamide antibiotics deciphered Cyanobacteria and Proteobacteria microbiome in huanglongbing-affected Citrus paradise and Citrus limon. | [General Description]
Chemical structure: sulfonamide | [Biochem/physiol Actions]
Sulfathiazole is a sulfonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfathiazole is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA), which is required for bacterial synthesis of folic acid. It is active against Gram positive bacteria, Gram negative bacteria and Chlamydia. Mode of resistance is via the alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis. |
|
|