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Sulfathiourea

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Sulfathiourea
Clinical data
Other names(4-aminophenyl)sulfonylthiourea
ATC code
Identifiers
  • 4-amino-N-(aminocarbonothioyl)benzenesulfonamide
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEBI
CompTox Dashboard(EPA)
ECHA InfoCard100.007.457Edit this at Wikidata
Chemical and physical data
FormulaC7H9N3O2S2
Molar mass231.29 g·mol−1
3D model (JSmol)
  • O=S(=O)(c1ccc(N)cc1)NC(=S)N
  • 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 asulfonamideantibacterial.[1]

References

[edit]
  1. ^Schoog M (November 1953). "[Sulfathiourea, chemistry, pharmacology and clinical aspects]".Zeitschrift für Haut- und Geschlechtskrankheiten (in German).15 (10):315–8.PMID 13137202.
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/orDNA 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
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins


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