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Nifurtimox

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.

Product Specifications

CAS Number

23256-30-6

Product Name Alternative

BAY-2502 | BAY-A-2502

Field of Research

Pharmacology & Drug Discovery

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

Molecular Formula

C10H13N3O5S

Molecular Weight

287.3

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

(E) -3-methyl-4- (((5-nitrofuran-2-yl) methylene) amino) thiomorpholine 11-dioxide

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