Nifurtimox

CAS No. 23256-30-6

Nifurtimox( BAY-2502 | BAY-A-2502 )

Catalog No. M20095 CAS No. 23256-30-6

Nifurtimox is an antiprotozoal agent (IC50s = 9.91 12.28 and 10.44 μM against Taluahuén LQ and Brener strains of T. cruzi- epimastigotes respectively).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 155 In Stock
25MG 303 In Stock
50MG 533 In Stock
100MG 767 In Stock
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Biological Information

  • Product Name
    Nifurtimox
  • Note
    Research use only, not for human use.
  • Brief Description
    Nifurtimox is an antiprotozoal agent (IC50s = 9.91 12.28 and 10.44 μM against Taluahuén LQ and Brener strains of T. cruzi- epimastigotes respectively).
  • Description
    Nifurtimox is an antiprotozoal agent (IC50s = 9.91 12.28 and 10.44 μM against Taluahuén LQ and Brener strains of T. cruzi- epimastigotes respectively).(In Vitro):Nifurtimox affects enzyme activity of lactate dehydrogenase (LDH). To differentiate if this effect is a result of a reduced LDH activity or a shift in pyruvate metabolism due to activation of PDH, the enzyme activity of LDH is determined after 4 h treatment with 50 μg/mL Nifurtimox. Compared to the untreated control, the LDH activity is significantly reduced for LA-N-1 (P=0.005), IMR-32 (P=0.009), LS (P=0.0035) and SK-N-SH (P=0.0065). Nifurtimox reduces cell viability and induces cell cycle arrest and apoptosis in neuroblastoma cells. To characterize the cytotoxic impacts of Nifurtimox on neuroblastoma, 4 cell lines are subjected to several experiments. Cell viability is reduced for all 4 neuroblastoma cell lines after 24 h incubation with 50 μg/mL to an average of 66%, 63%, 62% and 75% (LA-N-1, IMR-32 LS and SK-N-SH, respectively). The reduction is significant compared to the untreated control (P<0.01) and the vehicle control with DMSO (P<0.05) for all cell lines.
  • In Vitro
    Nifurtimox affects enzyme activity of lactate dehydrogenase (LDH). To differentiate if this effect is a result of a reduced LDH activity or a shift in pyruvate metabolism due to activation of PDH, the enzyme activity of LDH is determined after 4 h treatment with 50 μg/mL Nifurtimox. Compared to the untreated control, the LDH activity is significantly reduced for LA-N-1 (P=0.005), IMR-32 (P=0.009), LS (P=0.0035) and SK-N-SH (P=0.0065). Nifurtimox reduces cell viability and induces cell cycle arrest and apoptosis in neuroblastoma cells. To characterize the cytotoxic impacts of Nifurtimox on neuroblastoma, 4 cell lines are subjected to several experiments. Cell viability is reduced for all 4 neuroblastoma cell lines after 24 h incubation with 50 μg/mL to an average of 66%, 63%, 62% and 75% (LA-N-1, IMR-32 LS and SK-N-SH, respectively). The reduction is significant compared to the untreated control (P<0.01) and the vehicle control with DMSO (P<0.05) for all cell lines.
  • In Vivo
    ——
  • Synonyms
    BAY-2502 | BAY-A-2502
  • Pathway
    Microbiology/Virology
  • Target
    Parasite
  • Recptor
    Parasite
  • Research Area
    Cancer
  • Indication
    Medulloblastoma; Neuroblastoma

Chemical Information

  • CAS Number
    23256-30-6
  • Formula Weight
    287.3
  • Molecular Formula
    C10H13N3O5S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 50 mg/mL (174.03 mM);Water: Insoluble
  • SMILES
    CC1CS(=O)(=O)CCN1\N=C\c1ccc(o1)[N+]([O-])=O
  • Chemical Name
    (E)-3-methyl-4-(((5-nitrofuran-2-yl)methylene)amino)thiomorpholine 11-dioxide

Shipping & Storage Information

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

Reference

1.Maya JD et al. Trypanosoma cruzi: effect and mode of action of nitroimidazole and nitrofuran derivatives. Biochem Pharmacol. 2003 Mar 15;65(6):1999-12006.
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