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Sulfisomidine

Catalog No.
BA1099
An orally active, short-acting sulfonamide antibacterial agent.
Grouped product items
SizePriceStock Qty
100mg
$50.00
In stock
200mg
$88.00
In stock
500mg
$124.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Email: [email protected]

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Background

Sulfisomidine (CAS No.: 515-64-0) is a short-acting sulfonamide antibacterial compound widely used as a biochemical tool in studies of microbial metabolism and enzyme inhibition. It exerts its primary activity by competitively interfering with para-aminobenzoic acid (PABA) utilization in the bacterial tetrahydrofolate synthesis pathway, thereby disrupting folate-dependent metabolic processes essential for bacterial growth. In addition to its antimicrobial mechanism, sulfisomidine has been identified as an inhibitor of human serum paraoxonase 1 (hPON1), exhibiting mixed-type inhibition with activity in the millimolar range, making it relevant for investigations into enzyme kinetics, oxidative stress regulation, and lipid metabolism pathways. Experimental applications often include in vitro enzyme assays and cell-based models to evaluate hPON1 modulation or antibacterial activity, with concentrations typically selected around reported inhibitory ranges depending on assay design. Furthermore, sulfisomidine has been utilized in environmental and degradation studies, such as advanced oxidation processes, to examine transformation pathways and ecological fate of sulfonamide compounds. Overall, this molecule serves as a versatile research reagent in microbiology, enzymology, and environmental science for probing folate biosynthesis inhibition and paraoxonase-related biochemical functions.

Chemical Properties

Physical AppearanceA solid
Storage -20°C
M.Wt278.33
Cas No.515-64-0
FormulaC12H14N4O2S
SynonymsSulfisomidine, sulfamethin, Sulfaisodimidine, Sulfadimetine
Solubility≥5 mg/mL in DMSO with ultrasonic; insoluble in EtOH; ≥2.44 mg/mL in H2O with ultrasonic
Chemical Name4-amino-N-(2,6-dimethylpyrimidin-4-yl)benzenesulfonamide
Canonical SMILESO=S(NC1=NC(C)=NC(C)=C1)(C2=CC=C(N)C=C2)=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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