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Sulfisoxazole Acetyl

Catalog No.
B4954
Sulfonamide antibacterial agent
Grouped product items
SizePriceStock Qty
5mg
$50.00
In stock
10mg
$65.00
In stock
50mg
$140.00
In stock
100mg
$210.00
In stock
200mg
$348.00
In stock
500mg
$556.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

Sulfisoxazole Acetyl (CAS No.: 80-74-0) is an acetylated derivative of the sulfonamide antibiotic sulfisoxazole and functions as a synthetic analog of para-aminobenzoic acid (PABA), placing it within the class of small-molecule inhibitors targeting bacterial folate biosynthesis. This compound exerts its biological activity through competitive inhibition of the bacterial enzyme dihydropteroate synthase, thereby blocking the incorporation of PABA into dihydrofolic acid and disrupting the downstream production of folic acid, purines, and pyrimidines essential for nucleic acid synthesis. As a result, sulfisoxazole acetyl induces bacteriostatic or bactericidal effects in susceptible microbial systems, making it a valuable tool compound for investigating folate-dependent metabolic pathways and antimicrobial resistance mechanisms. In vitro studies with sulfonamide analogs, including sulfisoxazole derivatives, typically demonstrate activity in the low micromolar to millimolar range depending on the organism and assay conditions. Sulfisoxazole acetyl is widely utilized in microbiological and biochemical research to evaluate enzyme inhibition, probe bacterial growth dynamics, and serve as a reference compound in antimicrobial screening assays, with experimental concentrations or dosing regimens varying according to specific study designs and model systems.

Chemical Properties

Physical AppearanceA solid
Storage -20°C
M.Wt309.34
Cas No.80-74-0
FormulaC13H15N3O4S
SynonymsLipo Gantrisin, Gantrisin Pediatric, Acetylsulfisoxazole
Solubilityinsoluble in H2O; insoluble in EtOH; ≥14.15 mg/mL in DMSO
Chemical NameN-((4-aminophenyl)sulfonyl)-N-(3,4-dimethylisoxazol-5-yl)acetamide
Canonical SMILESO=S(C1=CC=C(N([H])[H])C=C1)(N(C(C)=O)C2=C(C)C(C)=NO2)=O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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