Sulfathiazole Explained

Verifiedrevid:470473528
Iupac Name:4-amino-N-(1,3-thiazol-2-yl)benzenesulfonamide
Cas Number:72-14-0
Atc Prefix:D06
Atc Suffix:BA02
Pubchem:5340
Drugbank:DB06147
Chemspiderid:5148
Unii:Y7FKS2XWQH
Kegg:D01047
Chebi:9337
Chembl:437
C:9
H:9
N:3
O:2
S:2
Smiles:O=S(=O)(Nc1nccs1)c2ccc(N)cc2
Stdinchi: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)
Stdinchikey:JNMRHUJNCSQMMB-UHFFFAOYSA-N
Melting Point:202
Melting High:202.5

Sulfathiazole is an organosulfur compound used as a short-acting sulfa drug.[1] Formerly, it was a common oral and topical antimicrobial, until less toxic alternatives were discovered.[2]

Sulfathiazole exists in various forms (polymorphs). The imine tautomer is dominant in solid samples.[3]

Cultural references

Notes and References

  1. Encyclopedia: Mertschenk B, Beck F, Bauer W . Thiourea and Thiourea Derivatives. Ullmann's Encyclopedia of Industrial Chemistry. 2002. Wiley-VCH. 10.1002/14356007.a26_803. 3527306730 .
  2. Rouf A, Tanyeli C . Bioactive thiazole and benzothiazole derivatives . European Journal of Medicinal Chemistry . 97 . 911–27 . June 2015 . 25455640 . 10.1016/j.ejmech.2014.10.058 .
  3. Kruger GT, Gafner G . The crystal structure of sulphathiazole II. . Acta Crystallographica Section B . February 1971 . 27 . 2 . 326–33 . 10.1107/S0567740871002176 . 1971AcCrB..27..326K . free .
  4. Book: Chapman FS . The Jungle is Neutral . WW norton . 1949 . 108 .