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
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 43 In Stock
5MG 39 In Stock
10MG 68 In Stock
25MG 134 In Stock
50MG 226 In Stock
100MG 323 In Stock
200MG 448 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

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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