货号:A232738
同义名:
IKK2 Inhibitor V
IMD-0354(IKK2抑制剂V)选择性抑制IKKβ,减少NF-κB活性。IMD0354还抑制TNF-α诱导的NF-κB转录活性,IC50为1.2 μM。
规格 | 价格 | 会员价 | 库存 | 数量 | |||
---|---|---|---|---|---|---|---|
{[ item.pr_size ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
产品名称 | NF-κB ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PDTC ammonium | ✔ | 98% | |||||||||||||||||
QNZ |
++++
NF-κB, IC50: 11 nM |
99%+ | |||||||||||||||||
Sodium 4-Aminosalicylate Dihydrate | ✔ | 98% | |||||||||||||||||
Sodium Salicylate | ✔ | 95% | |||||||||||||||||
Parthenolide | ✔ | p53 | 97% HPLC | ||||||||||||||||
JSH-23 |
+
NF-κB, IC50: 7.1 μM |
98% | |||||||||||||||||
Phenethyl caffeate | ✔ | 98% | |||||||||||||||||
Andrographolide | ✔ | 98+% | |||||||||||||||||
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。 |
描述 | IMD-0354, also known as IKK2 Inhibitor V, is a selective inhibitor of IKKβ that suppresses the activity of the NF-κB pathway through IKKβ inhibition[1]. IMD0354 inhibits TNF-α-induced NF-κB transcriptional activity with an IC50 of 1.2 µM[2]. IMD-0354 inhibits NF-κB activity in HMC-1 cells, thereby completely suppressing growth factor-dependent proliferation of mast cells. Cell proliferation is entirely inhibited when IMD-0354 treatment suppresses the DNA binding activity of NF-κB. IMD-0354 inhibits cell proliferation in a time- and dose-dependent manner. Compared to STI571, the inhibitory effect of IMD-0354 is significant even at lower concentrations[1]. |
细胞系 | 浓度 | 检测类型 | 检测时间 | 活性说明 | 数据源 |
HFF cells | Function assay | 72 h | Antiapicomplexan activity against Toxoplasma gondii RH tachyzoites expressing yellow fluorescent protein infected in HFF cells after 72 hrs by fluorescence assay, IC50=0.016 μM | 22970937 |
Animal study | Administered at a dose of 5 mg/kg daily, IMD-0354 significantly inhibits tumor expansion in nude mice implanted with established MDA-MB-231 tumors. Tumor progression is suppressed in mice treated with IMD-0354[3]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.61mL 0.52mL 0.26mL |
13.03mL 2.61mL 1.30mL |
26.06mL 5.21mL 2.61mL |
CAS号 | 978-62-1 |
分子式 | C15H8ClF6NO2 |
分子量 | 383.67 |
SMILES Code | O=C(NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1)C2=CC(Cl)=CC=C2O |
MDL No. | MFCD00218820 |
别名 | IKK2 Inhibitor V |
运输 | 蓝冰 |
InChI Key | CHILCFMQWMQVAL-UHFFFAOYSA-N |
Pubchem ID | 5081913 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, store in freezer, under -20°C |
溶解方案 |
DMSO: 105 mg/mL(273.67 mM),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 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
|
动物实验配方 |
2% DMSO+5% Tween 80+0.5% CMC Na +water 3 mg/mL |