Sulfisoxazole Acetyl
Sulfisoxazole acetyl is the acetyl ester prodrug of sulfisoxazole used in pediatric oral liquid formulations to mask the bitter taste of sulfisoxazole, providing equivalent systemic antibacterial activity after intestinal hydrolysis to the parent compound. See sulfisoxazole for complete pharmacological details.
Moleküler Ağırlık
309,3400 g/mol
LogP
1,30
TPSA
115,00 Ų
Lipinski RO5
Geçer
Etki Mekanizması
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
2D Yapı
Cite this structure
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SMILES
CC(=O)N(c1onc(C)c1C)S(=O)(=O)c1ccc(N)cc1
InChI
InChI=1S/C13H15N3O4S/c1-8-9(2)15-20-13(8)16(10(3)17)21(18,19)12-6-4-11(14)5-7-12/h4-7H,14H2,1-3H3
Molecular Formula
C13H15N3O4S
HBD / HBA
1 / 6
Döndürülebilir Bağlar
3
Ağır Atomlar
21
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Sıkça Sorulan Sorular
Sulfisoxazole acetyl is the acetyl ester prodrug of sulfisoxazole used in pediatric oral liquid formulations to mask the bitter taste of sulfisoxazole, providing equivalent systemic antibacterial activity after intestinal hydrolysis to the parent compound. See sulfisoxazole for complete pharmacological details.
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Yes, Sulfisoxazole Acetyl is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200910. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6662. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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