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Sulfadicramide

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Chemical compound

Pharmaceutical compound
Sulfadicramide
Clinical data
ATC code
Identifiers
IUPAC name
  • N-(4-aminophenyl)sulfonyl-3-methylbut-2-enamide
CAS Number
PubChem CID
DrugBank
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.003.727 Edit this at Wikidata
Chemical and physical data
FormulaC11H14N2O3S
Molar mass254.30 g·mol
3D model (JSmol)
SMILES
  • CC(=CC(=O)NS(=O)(=O)C1=CC=C(C=C1)N)C
InChI
  • InChI=InChI=1S/C11H14N2O3S/c1-8(2)7-11(14)13-17(15,16)10-5-3-9(12)4-6-10/h3-7H,12H2,1-2H3,(H,13,14)
  • Key:XRVJPLDTMUSSDE-UHFFFAOYSA-N

Sulfadicramide (marketed as Irgamid) is an anti-infective.

References

  1. Grześkowiak E, Partyka D, Simon M, Zgrabczyńska M, Wiśniewska A (2001). "Technology and physico-chemical evaluation of solid ocular inserts containing sulfadicramide and hyaluronic acid". Acta Poloniae Pharmaceutica. 58 (6): 453–458. PMID 12197618.
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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