Sulfisoxazole

Sulfisoxazole

Catalog Number:
M001342403TOK
Mfr. No.:
TOK-S120
Price:
$221
  • Size:
    5g
    Quantity:
    Add to Cart:
      • Overview
        • Sulfisoxazole is a bioactive small molecule and broad-spectrum sulfanilamide antibacterial agent with an oxazole substituent. It is an ETA selective endothelin receptor antagonist (ETAR antagonist). It is a synthetic analog of the natural compound para-aminobenzoic acid (PABA).

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          Background

          Sulfisoxazole competes with PABA for the bacterial dihydropteroate synthase, thus preventing incorporation of PABA into dihydrofolic acid, the precursor to folic acid. Folic acid is a coenzyme in the synthesis of purines and pyrimidines, leading to reduced cell growth and cell death. Unlike bacteria (and fungi/ plants) that synthesize their own folic acid, mammals do not, and thus are unaffected by PABA inhibitors.

      • Properties
        • CAS Number
          127-69-5
          Molecular Formula
          C11H13N3O3S
          Molecular Weight
          267.30
          Appearance
          Solid
          Solubility
          soluble in DMSO. acetone. slightly soluble in alcohol
          Other Properties
          Source: Synthetic
          Purity Level: ≥98% (HPLC)
          Storage
          2-8°C

          * For research use only

      • Applications
        • Application Description
          Spectrum: Broad-spectrum against a range of Gram-positive and Gram-negative bacteria including otitis media.

          Microbiology Applications: Sulfisoxazole is commonly used in clinical in vitro microbiological antimicrobial susceptibility tests (Sensi-Disc, from BD) against Gram- positive and Gram-negative bacteria.Sulfisoxazole has IC50 of 0.6 uM for ETA receptor, and 22 uM for rETA receptor. Sulfisoxazole was used in a novel engineered E. coli 12-member reporter panel of bioluminescent reporter stains, constructed using a novel non-antibiotic selection system, to survey environmental residues. The selectivity marker was developed based on the requirement for tryptophan, and folic acid-free medium was employed (Melamed et al, 2012).

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