PfDHODH-IN-2
目录号: PL06541 纯度: ≥99%
CAS No. :425629-94-3
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中文名称
PfDHODH-IN-2
英文名称
PfDHODH-IN-2
英文别名
ethyl 2-[(4-chlorophenyl)amino]-4-oxo-4,5-dihydro-3-thiophenecarboxylate;PfDHODH-IN-2
Cas No.
425629-94-3
分子式
C13H12NO3Scl
分子量
297.76
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
PfDHODH-IN-2 是一种有效的恶性疟原虫二氢旋酸脱氢酶 (PfDHODH) 抑制剂,其 IC50 值为 1.11 µM。PfDHODH-IN-2 具有抗疟作用,可用于疟疾的研究。
生物活性
PfDHODH-IN-2, a dihydrothiophenone derivative (Compound 11), is a potent Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH) inhibitor with an IC 50 of 1.11 μM. PfDHODH-IN-2 acts as an antimalarial agent and can be used for the research of malaria.
性状
Solid
IC50 & Target[1][2]
IC50: 1.113 μM (PfDHODH)
IC50: >50 μM ( hDHODH)
体外研究(In Vitro)
Malaria is a global parasitic infectious disease caused by Plasmodium parasites, among which Plasmodium falciparum is the most dangerous one with the highest rates of complications and mortality.
PfDHODH-IN-2 shows an overall selectivity for PfDHODH (IC50=1.113 μM) over hDHODH (IC50>50 μM). PfDHODH-IN-2 demonstrats in vitro potency against the 3D7 and Dd2 strains of P. falciparum with IC50 values of both >20 μM, respectively in whole cell assays.
has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Minghao Xu, et al. Novel selective and potent inhibitors of malaria parasite dihydroorotate dehydrogenase: discovery and optimization of dihydrothiophenone derivatives. J Med Chem. 2013 Oct 24;56(20):7911-24.
溶解度数据
In Vitro: DMSO : 12.5 mg/mL (41.98 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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