
CAS 967-80-6: Sulfaquinoxaline sodium
Formula:C14H12N4O2S·Na
InChI:InChI=1S/C14H12N4O2S.Na/c15-10-5-7-11(8-6-10)21(19,20)18-14-9-16-12-3-1-2-4-13(12)17-14;/h1-9H,15H2,(H,17,18);
InChI key:InChIKey=UBDSWJJGFQSVLE-UHFFFAOYSA-N
SMILES:N(S(=O)(=O)C1=CC=C(N)C=C1)C2=NC3=C(N=C2)C=CC=C3.[Na]
Synonyms:- Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, monosodium salt
- Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, sodium salt (1:1)
- Embazin
- N'1-Quinoxalin-2-ylsulphanilamide sodium salt
- Noxal
- Noxal (antimicrobial)
- Sodium 2-sulfanilamidoquinoxaline
- Sodium [(4-Aminophenyl)Sulfonyl](Quinoxalin-6-Yl)Azanide
- Sodium sulfaquinoxaline
- Sodium, (N<sup>1</sup>-2-quinoxalinylsulfanilamido)-
- Sulfanilamide, N<sup>1</sup>-2-quinoxalinyl-, monosodium salt
- See more synonyms
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Found 11 products.
Sulfaquinoxaline sodium salt
CAS:Formula:C14H11N4NaO2SPurity:≥ 95.0%Color and Shape:White to yellow powderMolecular weight:322.32Sulfaquinoxaline sodium salt
CAS:Sulfaquinoxaline sodium salt (SQ-Na) is a veterinary broad-spectrum antimicrobial agent, which can be used to prevent coccidiosis and bacterial infections.Formula:C14H11N4NaO2SPurity:99.72%Color and Shape:SolidMolecular weight:322.32Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, monosodium salt
CAS:Formula:C14H11N4NaO2SPurity:98%Color and Shape:SolidMolecular weight:322.3175Sulfaquinoxaline sodium 100 µg/mL in Acetonitrile
CAS:Formula:C14H11N4O2S·NaColor and Shape:Single SolutionMolecular weight:322.32Sulfaquinoxaline sodium salt
CAS:Sulfaquinoxaline sodium salt is a dpp-iv inhibitor that has been shown to be effective in the treatment of inflammatory bowel disease. The drug inhibits the enzyme dipeptidyl peptidase 4, which is involved in the degradation of immunoreactive insulin and glucagon-like peptide-1. Sulfaquinoxaline sodium salt produces an antimicrobial effect by inhibiting microbial growth and also has a synergic effect with other antibiotics such as amoxicillin. As well as being used to treat bowel diseases, sulfaquinoxaline sodium salt is also used for sample preparation before DNA or RNA extraction. It can be used as a co-substrate with sodium carbonate to precipitate proteins in biological samples, such as urine or stool samples, or wastewater before treatment.Formula:C14H12NaN4O2SPurity:Min. 95%Molecular weight:323.33 g/molSulfaquinoxaline Sodium Salt
CAS:Stability Hygroscopic Applications Coccidiostat. References Mathis, G.F., et al.: Poult. Sci., 63, 1149 (1984), Cassiano, N., et al.: Anal. Bioanal. Chem., 384, 1462 (2006), Chung, H., et al.: Food Chem., 113, 297 (2009),Formula:C14H11N4O2S·NaColor and Shape:Off-WhiteMolecular weight:322.32Sodium ((4-Aminophenyl)Sulfonyl)(Quinoxalin-2-Yl)Amide
CAS:Sodium ((4-Aminophenyl)Sulfonyl)(Quinoxalin-2-Yl)AmidePurity:98%Molecular weight:322.32g/mol