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NU 7026 {[allProObj[0].p_purity_real_show]}

货号:A183964 同义名: LY293646;DNA-PK Inhibitor II

NU7026 is a potent and selective inhibitor of DNA-PK with IC50 of 0.23 μM.

NU 7026 化学结构 CAS号:154447-35-5
NU 7026 化学结构
CAS号:154447-35-5
NU 7026 3D分子结构
CAS号:154447-35-5
NU 7026 化学结构 CAS号:154447-35-5
NU 7026 3D分子结构 CAS号:154447-35-5
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NU 7026 纯度/质量文件 产品仅供科研

货号:A183964 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 DNA-PK 其他靶点 纯度
PI-103 ++

DNA-PK, IC50: 23 nM

99%+
CC-115 +++

DNA-PK, IC50: 0.013 μM

mTOR 98+%
Samotolisib 99%+
NU 7026 +

DNA-PK, IC50: 0.23 μM

PI3K 98+%
PIK-75 HCl ++++

DNA-PK, IC50: 2 nM

99%+
PP121 +

DNA-PK, IC50: 60 nM

PDGFR,VEGFR 99%+
KU-0060648 ++++

DNA-PK, IC50: 5 nM

99%
KU-57788 +++

DNA-PK, IC50: 14 nM

99%+
LTURM34 ++

DNA-PK, IC50: 0.034 μM

98%+
SF2523 +++

DNA-PK, IC50: 9 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

NU 7026 生物活性

靶点
  • PI3K

    PI3K, IC50:13 μM

  • DNA-PK

    DNA-PK, IC50:0.23 μM

描述 NU 7026 (LY293646) is a novel specific DNA-PK inhibitor with IC50 of 0.23 μM, also inhibits PI3K with IC50 of 13 μM[1]. NU7026 enhances the cytotoxic effects of ionizing radiation (IR) in cells proficient in DNA-PK, evidenced by a potentiation factor at 90% cell kill (PF90) of 1.51±0.04[1]. In vitro, at a 10 μM concentration, which itself is not toxic to cells, NU7026 4-hour exposure combined with 3 Gy of radiation to significantly increase radiosensitivity in CH1 human ovarian cancer cells[3].
体内研究

After intravenous delivery at 5 mg/kg to mice, NU7026 shows rapid plasma clearance at a rate of 0.108 L/h, primarily due to extensive metabolism. Its bioavailability after interperitoneal (i.p.) and oral (p.o.) administration at 20 mg/kg is observed to be 20% and 15%, respectively[3].

体外研究

NU 7026 (LY293646) is a novel specific DNA-PK inhibitor with IC50 of 0.23 μM, also inhibits PI3K with IC50 of 13 μM[1].

NU7026 enhances the cytotoxic effects of ionizing radiation (IR) in cells proficient in DNA-PK, evidenced by a potentiation factor at 90% cell kill (PF90) of 1.51±0.04[1].

In vitro, at a 10 μM concentration, which itself is not toxic to cells, NU7026 4-hour exposure combined with 3 Gy of radiation to significantly increase radiosensitivity in CH1 human ovarian cancer cells[3].

NU 7026 细胞研究

细胞系 浓度 检测类型 检测时间 活动说明 数据源
HeLa cells Function assay Inhibition of DNA dependent protein kinase isolated from HeLa cells, IC50=0.23 μM 15658870
HeLa cells Function assay Inhibition of mTOR protein isolated from HeLa cells, IC50=6.4 μM 15658870

NU 7026 参考文献

[1]Veuger SJ, et al. Radiosensitization and DNA repair inhibition by the combined use of novel inhibitors of DNA-dependent protein kinase and poly(ADP-ribose) polymerase-1. Cancer Res. 2003 Sep 15;63(18):6008-15.

[2]Nutley BP, et al. Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026. Br J Cancer. 2005 Oct 31;93(9):1011-8.

NU 7026 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.55mL

0.71mL

0.36mL

17.77mL

3.55mL

1.78mL

35.55mL

7.11mL

3.55mL

NU 7026 技术信息

CAS号154447-35-5
分子式C17H15NO3
分子量 281.306
别名 LY293646;DNA-PK Inhibitor II
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Sealed in dry,2-8°C

溶解度

DMSO: 2 mg/mL(7.11 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

1% DMSO+30% polyethylene glycol+1% Tween 80+water 30 mg/mL suspension

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