Structure via PubChem · Public domain (PubChem)
sulfaquinoxaline
Sign in to saveSulfaquinoxaline (IUPAC name: '4-Amino-N-2-quinoxalinylbenzenesulfonamide') is a veterinary medicine which can be given to cattle and sheep to treat coccidiosis.
Chemical data
- Formula
- C14H12N4O2S
- Molecular weight
- 300.34 g/mol
- IUPAC name
- 4-amino-N-quinoxalin-2-ylbenzenesulfonamide
- SMILES
- C1=CC=C2C(=C1)N=CC(=N2)NS(=O)(=O)C3=CC=C(C=C3)N
- InChIKey
- NHZLNPMOSADWGC-UHFFFAOYSA-N
- XLogP
- 1.7
- Polar surface area
- 106 Ų
- H-bond donors
- 2
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
341 papers- Sulfaquinoxaline Toxicosis in a Juvenile Broiler Breeder Flock.Avian diseases · 2023
- Sulfaquinoxaline Oxidation and Toxicity Reduction by Photo-Fenton Process.International journal of environmental research and public health · 2021
- Sulfaquinoxaline oxidation by UV-C activated sodium persulfate: Degradation kinetics and toxicological evaluation.Water environment research : a research publication of the Water Environment Federation · 2019
- Identification of folic acid and sulfaquinoxaline using a heterometallic Zn-Eu MOF as a sensor.Dalton transactions (Cambridge, England : 2003) · 2023
- History of the discovery of sulfaquinoxaline as a coccidiostat.The Journal of parasitology · 2008
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 300.068
Show 4 more facts
- chemical formula
- C₁₄H₁₂N₄O₂S
- canonical SMILES
- C1=CC=C2C(=C1)N=CC(=N2)NS(=O)(=O)C3=CC=C(C=C3)N
- isomeric SMILES
- C1=CC=C2C(=C1)N/C(=N/S(=O)(=O)C3=CC=C(C=C3)N)/C=N2
- subject has role
- antiprotozoal
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Sulfaquinoxaline (IUPAC name: '4-Amino-N-2-quinoxalinylbenzenesulfonamide') is a veterinary medicine which can be given to cattle and sheep to treat coccidiosis.
==References==
Excerpted from Wikipedia’s “sulfaquinoxaline” article, available under the CC BY-SA 4.0 licence.