21312-10-7
Chemical Structure
N4-Acetylsulfamethoxazole
Synonym(s): Acetylsulfamethoxazole
- CAS No.: 21312-10-7
- Formula:C12H13N3O4S
- Molecular Weight:295.31
IUPAC Name: N-(4-(N-(5-methylisoxazol-3-yl)sulfamoyl)phenyl)acetamide
InChIKey: GXPIUNZCALHVBA-UHFFFAOYSA-N
SMILES: CC(NC1=CC=C(C=C1)S(=O)(NC2=NOC(C)=C2)=O)=O
Biological Activity: N4-Acetylsulfamethoxazole (Acetylsulfamethoxazole) is the N4-acetylated metabolite of Sulfamethoxazole (HY-B0322)[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N4-Acetylsulfamethoxazole | 99.72% | N4-Acetylsulfamethoxazole (Acetylsulfamethoxazole) is the N4-acetylated metabolite of Sulfamethoxazole (HY-B0322). | ||||||||||||||||||||
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N4-Acetylsulfamethoxazole (Standard) | ≥98% | N4-Acetylsulfamethoxazole (Acetylsulfamethoxazole) Standard of N4-Acetylsulfamethoxazole (HY-W013266). This product is intended for research and analytical applications. N4-Acetylsulfamethoxazole (Acetylsulfamethoxazole) is the N4-acetylated metabolite of Sulfamethoxazole (HY-B0322). | ||||||||||||||||||||
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N4-Acetylsulfamethoxazole-13C6 | N4-Acetylsulfamethoxazole-13C6 (Acetylsulfamethoxazole-13C6) is the 13C-labeled N4-Acetylsulfamethoxazole (HY-W013266). N4-Acetylsulfamethoxazole (Acetylsulfamethoxazole) is a metabolite of?Sulfamethoxazole (HY-B0322). Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic, used for bacterial infections. | |||||||||||||||||||||
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N4-Acetylsulfamethoxazole-d4 | N4-Acetylsulfamethoxazole-d4 (Acetylsulfamethoxazole-d4) is the deuterium labeled N4-Acetylsulfamethoxazole (HY-W013266). N4-Acetylsulfamethoxazole (Acetylsulfamethoxazole) is the N4-acetylated metabolite of Sulfamethoxazole (HY-B0322). | |||||||||||||||||||||
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- [1]. van der Ven AJ, et al. Formation and elimination of sulphamethoxazole hydroxylamine after oral administration of sulphamethoxazole. Br J Clin Pharmacol. 1994;38(2):147-150. [Content Brief]
- [2]. Straub J O. Aquatic environmental risk assessment for human use of the old antibiotic sulfamethoxazole in Europe. Environmental toxicology and chemistry, 2016, 35(4): 767-779.