BQR-695 (Synonyms: NVP-BQR695)
目录号: PL08865 纯度: ≥99%
CAS No. :1513879-21-4
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中文名称
BQR-695
英文名称
BQR-695
英文别名
BQR-695
Cas No.
1513879-21-4
分子式
C19H20N4O3
分子量
352.39
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
BQR-695 是一种 PI4KIIIβ 抑制剂,对于人类和疟原虫 PI4KIIIβ 的 IC50 值分别为 80 和 3.5 nM。
生物活性
BQR-695 is a PI4KIIIβ inhibitor with IC 50 s of 80 and 3.5 nM for human PI4KIIIβ and Plasmodium variant of PI4KIIIβ, respectively.
性状
Solid
IC50 & Target[1][2]
human PI4KIIIβ 80 nM (IC50) Plasmodium pan> <
体外研究(In Vitro)
Treatment with 0.5 μM of either KAI407 or BQR695 causes GFP-PH to redistribute to the parasite plasma membrane, consistent with depletion of intracellular PI4P upon inhibition of PfPI4K function. BQR695 shows no evidence of toxicity against mature red blood cells (RBCs), induces a schizont-stage arrest indistinguishable from that observed in imidazopyrazine-treated parasites and exhibits cross-resistance with the imidazopyrazine-resistant lines. 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]. Fowler ML, et al. Using hydrogen deuterium exchange mass spectrometry to engineer optimized constructs for crystallization of protein complexes: Case study of PI4KIIIβ with Rab11. Protein Sci. 2016 Apr;25(4):826-39.
[2]. McNamara CW, et al. Targeting Plasmodium PI(4)K to eliminate malaria. Nature. 2013 Dec 12;504(7479):248-253.
溶解度数据
In Vitro: DMSO : 50 mg/mL (141.89 mM; Need ultrasonic)配制储备液
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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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