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BQR-695 99%+

货号:A725053 同义名: NVP-BQR695 Ambeed 开学季,买赠积分,赢豪礼

BQR695 is a PI4K specific inhibitor with IC50 value of 80nM.

BQR-695 化学结构 CAS号:1513879-21-4
BQR-695 化学结构
CAS号:1513879-21-4
BQR-695 3D分子结构
CAS号:1513879-21-4
BQR-695 化学结构 CAS号:1513879-21-4
BQR-695 3D分子结构 CAS号:1513879-21-4
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BQR-695 纯度/质量文件 产品仅供科研

货号:A725053 标准纯度: 99%+
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BQR-695 生物活性

描述 Furthermore, treatment with 0.5 μM of either KAI407 or BQR695 leads to the redistribution of GFP-PHOsh2 to the plasma membrane of parasites, aligning with the depletion of intracellular PI4P upon inhibition of PfPI4K function. BQR695, in particular, demonstrates no toxicity against mature red blood cells (RBCs), induces a schizont-stage arrest similar to that observed with imidazopyrazine-treated parasites, and exhibits cross-resistance with imidazopyrazine-resistant lines[2].
体外研究

Furthermore, treatment with 0.5 μM of either KAI407 or BQR695 leads to the redistribution of GFP-PHOsh2 to the plasma membrane of parasites, aligning with the depletion of intracellular PI4P upon inhibition of PfPI4K function. BQR695, in particular, demonstrates no toxicity against mature red blood cells (RBCs), induces a schizont-stage arrest similar to that observed with imidazopyrazine-treated parasites, and exhibits cross-resistance with imidazopyrazine-resistant lines[2].

BQR-695 参考文献

[1]McNamara CW, et al. Targeting Plasmodium PI(4)K to eliminate malaria. Nature. 2013 Dec 12;504(7479):248-253.

BQR-695 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.84mL

0.57mL

0.28mL

14.19mL

2.84mL

1.42mL

28.38mL

5.68mL

2.84mL

BQR-695 技术信息

CAS号1513879-21-4
分子式C19H20N4O3
分子量 352.387
别名 NVP-BQR695
运输蓝冰
存储条件

粉末 Keep in dark place,Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 50 mg/mL(141.89 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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