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Sulfaphenazole

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(Redirected from Sulfafenazol) Chemical compound Pharmaceutical compound
Sulfaphenazole
Skeletal formula of sulfaphenazole
Space-filling model of the sulfaphenazole molecule
Clinical data
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
IUPAC name
  • 4-amino-N-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamide
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.007.624 Edit this at Wikidata
Chemical and physical data
FormulaC15H14N4O2S
Molar mass314.36 gยทmol
3D model (JSmol)
SMILES
  • O=S(=O)(c1ccc(N)cc1)Nc3ccnn3c2ccccc2
InChI
  • InChI=1S/C15H14N4O2S/c16-12-6-8-14(9-7-12)22(20,21)18-15-10-11-17-19(15)13-4-2-1-3-5-13/h1-11,18H,16H2
  • Key:QWCJHSGMANYXCW-UHFFFAOYSA-N
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Sulfaphenazole (or sulfafenazol) is a sulfonamide antibacterial.

References

  1. Browne SG (1961). "Trial of a long-acting sulfonamide sulfaphenazole (Orisul, Ciba), in the treatment of leprosy". International Journal of Leprosy. 29: 502โ€“5. PMID 13873771.
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
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins
Ophthalmologicals: anti-infectives (S01A)
Antibiotics
Sulfonamides
Antivirals
Fluoroquinolones
Other


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