CAS NO: | 23256-30-6 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Nifurtimox, an antiprotozoal agent, which is generally used for the treatment of infections withTrypanosomacruzi, has been used in the therapy of neuroblastoma. Nifurtimox affects enzyme activity oflactate dehydrogenase(LDH). | ||||||||||||||||
IC50& Target | Trypanosoma cruzi[1] | ||||||||||||||||
体外研究 (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[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 287.30 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C10H13N3O5S | ||||||||||||||||
CAS 号 | 23256-30-6 | ||||||||||||||||
中文名称 | 硝呋替莫 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 150 mg/mL(522.10 mM;Need ultrasonic) 配制储备液
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