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IMD-0560 99%+

货号:A724374 Ambeed 开学季,买赠积分,赢豪礼

IMD-0560 化学结构 CAS号:439144-66-8
IMD-0560 化学结构
CAS号:439144-66-8
IMD-0560 3D分子结构
CAS号:439144-66-8
IMD-0560 化学结构 CAS号:439144-66-8
IMD-0560 3D分子结构 CAS号:439144-66-8
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IMD-0560 纯度/质量文件 产品仅供科研

货号:A724374 标准纯度: 99%+
批次查询: 批次纯度:

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产品名称 NF-κB 其他靶点 纯度
Pyrrolidinedithiocarbamate ammonium 98%
QNZ ++++

NF-κB, IC50: 11 nM

99%+
Sodium 4-Aminosalicylate Dihydrate 99%+
Sodium Salicylate 99%+
Parthenolide p53 97% HPLC
JSH-23 +

NF-κB, IC50: 7.1 μM

98%
Phenethyl caffeate 99%+
Andrographolide 99%+
Curcumin Nrf2,HDAC 98%
SC75741 +++

NF-κB, EC50: 200 nM

99%+
CBL0137 HCl ++

NF-κB, EC50: 0.47 μM

p53 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。

IMD-0560 生物活性

描述 IMD-0560 is a novel IκB kinase β inhibitor. Pretreatment with IMD-0560 inhibited TNFα-induced IκBα degradation and p65 phosphorylation. IMD-0560 also inhibited TNFα-induced transcriptional activity. Pretreatment with IMD-0560 strongly inhibited TNFα-induced cell invasion. IMD-0560 inhibits the activity of MMP-9 by suppressing its expression[1].

IMD-0560 动物研究

Animal study Upon administration of IMD-0560, IMD-0560 reduces tumour bodies in animals in a dose-dependent manner. No tumours were found in some mice after IMD-0560 administration at a dose of 5 mg/kg. Tumour cell destruction was significantly reduced in the IMD-0560-treated group compared to the control group. Although the tumour size in the 5 mg/kg dose administered IMD-0560 treatment group was smaller than that in the 3 mg/kg IMD-0560 treatment group in the animal experiments, the inhibitory effect on zygapophyseal destruction was similar in the two treatment groups[1].

IMD-0560 参考文献

[1]Tada Y, et al. The novel IκB kinase β inhibitor IMD-0560 prevents bone invasion by oral squamous cell carcinoma. Oncotarget. 2014 Dec 15;5(23):12317-30.

IMD-0560 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.34mL

0.47mL

0.23mL

11.68mL

2.34mL

1.17mL

23.36mL

4.67mL

2.34mL

IMD-0560 技术信息

CAS号439144-66-8
分子式C15H8BrF6NO2
分子量 428.124
别名
运输蓝冰
存储条件

粉末 Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

无水乙醇: 50 mg/mL(116.79 mM),配合低频超声助溶,注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇

动物实验配方
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