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Sulfanitran

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Chemical compound Pharmaceutical compound
Sulfanitran
Clinical data
Other namesN-Acetyl-N-(para-nitrophenyl)sulfanilamide; APNPS; NSC-77120
Drug classAntibiotics; Sulfonamides
Identifiers
IUPAC name
  • N-phenyl]acetamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H13N3O5S
Molar mass335.33 gยทmol
3D model (JSmol)
SMILES
  • CC(=O)NC1=CC=C(C=C1)S(=O)(=O)NC2=CC=C(C=C2)(=O)
InChI
  • InChI=1S/C14H13N3O5S/c1-10(18)15-11-4-8-14(9-5-11)23(21,22)16-12-2-6-13(7-3-12)17(19)20/h2-9,16H,1H3,(H,15,18)
  • Key:GWBPFRGXNGPPMF-UHFFFAOYSA-N

Sulfanitran is a sulfonamide antibiotic which is used in the poultry industry. It is a component of Novastat, Polystat, and Unistat, brand names of feed additives for chickens used to control Coccidioides spp.

References

  1. Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 1โ€“. ISBN 978-1-4757-2085-3.
  2. Kreir J (1 January 1977). Gregarines, Haemogregarines, Coccidia, Plasmodia, and Haemoproteids. Elsevier. pp. 65โ€“. ISBN 978-0-323-16325-5.
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


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