Sulfathiourea

Chemical compound
  • J01EB08 (WHO)
Identifiers
  • 4-amino-N-(aminocarbonothioyl)benzenesulfonamide
CAS Number
  • 515-49-1
PubChem CID
  • 3000579
ChemSpider
  • 2272143 checkY
UNII
  • MXF9G4I1V5
KEGG
  • D07239 checkY
ChEBI
  • CHEBI:131723
CompTox Dashboard (EPA)
  • DTXSID4046868 Edit this at Wikidata
ECHA InfoCard100.007.457 Edit this at WikidataChemical and physical dataFormulaC7H9N3O2S2Molar mass231.29 g·mol−13D model (JSmol)
  • Interactive image
  • O=S(=O)(c1ccc(N)cc1)NC(=S)N
InChI
  • InChI=1S/C7H9N3O2S2/c8-5-1-3-6(4-2-5)14(11,12)10-7(9)13/h1-4H,8H2,(H3,9,10,13) checkY
  • Key:UEMLYRZWLVXWRU-UHFFFAOYSA-N checkY
  (verify)

Sulfathiourea is a sulfonamide antibacterial.[1]

References

  1. ^ Schoog M (November 1953). "[Sulfathiourea, chemistry, pharmacology and clinical aspects]". Zeitschrift für Haut- und Geschlechtskrankheiten (in German). 15 (10): 315–8. PMID 13137202.
  • v
  • t
  • e
Antibacterials that inhibit nucleic acid (J01E, J01M)
Antifolates
(inhibit bacterial
purine metabolism,
thereby inhibiting
DNA and RNA
synthesis)
DHFR inhibitor
Sulfonamides
(DHPS inhibitor)
Short-acting
Intermediate-acting
Long-acting
Other/ungrouped
Combinations
Other DHPS inhibitors
Quinolones
(inhibit bacterial
topoisomerase
and/or DNA gyrase,
thereby inhibiting
DNA replication)
1st generation
Fluoroquinolones
2nd generation
3rd generation
4th generation
Veterinary
Newer non-fluorinated
Related (DG)
Anaerobic DNA
inhibitors
Nitroimidazole derivatives
Nitrofuran derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins


Stub icon

This systemic antibiotic-related article is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e