Sulfamethoxazole

CAS No. 723-46-6

Sulfamethoxazole( NSC 147832 | Ro 4-2130 )

Catalog No. M15770 CAS No. 723-46-6

Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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50MG 41 In Stock
100MG 52 In Stock
200MG 63 In Stock
500MG 81 In Stock
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Biological Information

  • Product Name
    Sulfamethoxazole
  • Note
    Research use only, not for human use.
  • Brief Description
    Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic.
  • Description
    Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic. Target: Antibacterial Sulfonamides are structural analogs and competitive antagonists of para-aminobenzoic acid (PABA). (In Vitro):Sulfonamides are structural analogs and competitive antagonists of para-aminobenzoic acid (PABA). They inhibit normal bacterial utilization of PABA for the synthesis of folic acid, an important metabolite in DNA synthesis. The effects seen are usually bacteriostatic in nature. Folic acid is not synthesized in humans, but is instead a dietary requirement. This allows for the selective toxicity to bacterial cells (or any cell dependent on synthesizing folic acid) over human cells. Bacterial resistance to sulfamethoxazole is caused by mutations in the enzymes involved in folic acid synthesis that prevent the drug from binding to it.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    NSC 147832 | Ro 4-2130
  • Pathway
    Autophagy
  • Target
    Autophagy
  • Recptor
    DHPS| FolC
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    723-46-6
  • Formula Weight
    253.28
  • Molecular Formula
    C10H11N3O3S
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 23 mg/mL (90.8 mM); DMSO: 51 mg/mL (201.35 mM)
  • SMILES
    CC1=CC(NS(=O)(C2=CC=C(N)C=C2)=O)=NO1
  • Chemical Name
    4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Winstanley PA, et al. Antimicrob Agents ChemOthers. 1995 Apr;39(4):948-52.
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