| Weight | 309.347 g/mol |
|---|---|
| Formula | C13H15N3O4S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
Sulfisoxazole acetyl (80-74-0)
acetyl sulfisoxazole
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- Effects of lipids on bioavailability of sulfisoxazole acetyl, dicumarol, and griseofulvin in rats (Journal of Pharmaceutical Sciences, 1976)
- Influence of protein binding and metabolic interconversion on the disposition of sulfisoxazole and its N4-acetyl metabolite by the isolated perfused rat kidney. (Drug Metabolism and Disposition, 1984)
- Comparative studies on blood levels and urinary excretion of sulfisoxazole and acetyl sulfisoxazole. (Antibiotics and Chemotherapy, 1954)
- Saturable First-Pass Metabolism of Sulfisoxazole N1-Acetyl in Rats (Journal of Pharmaceutical Sciences, 1976)
- Effect of 4-N-acetyl-sulfisoxazole on the disposition of sulfisoxazole in the rat (International Journal of Pharmaceutics, 1979)
- Absorption and chemotherapeutic activity of acetyl sulfisoxazole suspended in an oil in water emulsion. (Antibiotic medicine & clinical therapy (New York), 1956)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - acetyl sulfisoxazole
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SMILESCC1=C(ON=C1C)N(C(=O)C)S(=O)(=O)C2=CC=C(C=C2)N
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InChIKeyJFNWFXVFBDDWCX-UHFFFAOYSA-N
- Pubchem - Sulfisoxazole acetyl
- Wikipedia - sulfisoxazole acetyl
Sulfafurazole (INN, also known as sulfisoxazole) is a sulfonamide antibacterial with an oxazole substituent. It has antibiotic activity against a wide range of Gram-negative and Gram-positive organisms. It is sometimes given in combination with erythromycin (see erythromycin/Sulfafurazole) or phenazopyridine.
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