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NF-&kappaB-IN-1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
NF-&kappaB-IN-1图片
规格:98%
分子量:530.57
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
NF-κB-IN-1,一种 4-亚芳基姜黄素类似物,是有效的 NF-κB 信号通路抑制剂。NF-κB-IN-1 直接抑制 IKK 来阻断 NF-κB 的激活。NF-κB-IN-1 可有效抑制肺癌细胞的活力并减弱 A549 细胞的克隆活性。
货号:ajcx32996
CAS:1227098-15-8
分子式:C31H30O8
分子量:530.57
溶解度:DMSO : 50 mg/mL (94.24 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

NF-κB-IN-1, a 4-arylidene crucumin analogue, is a potent NF-κB signaling pathway inhibitor. NF-κB-IN-1 directly inhibits IKK to block NF-κB activation. NF-κB-IN-1 effectively inhibits the viability of lung cancer cells and attenuates the clonogenic activity of A549 cells[1].

NF-κB-IN-1 (compound 17) (0.001-100 μM; 72 h) inhibits the growth of A549, H1944, H460 and H157 cells, with GI50s of 0.72, 0.07, 0.13, and 0.16 μM, respectively[1].NF-κB-IN-1 (0.5-25 μM; pretreated for 30 min or 4 h) potently blocks the IκB phosphorylation and degradation in A549 cells[1].NF-κB-IN-1 (0.1-100 μM; pretreated for 30 min) dose-dependently inhibits the TNFα-induced nuclear translocation of NF-κB in A549 cells, with an IC50s of 1.0 μM[1].NF-κB-IN-1 (0.1-0.4 μM; 9 d) inhibits lung cancer clonogenic activity[1].


[1]. Qiu X, et, al. Synthesis and identification of new 4-arylidene curcumin analogues as potential anticancer agents targeting nuclear factor-κB signaling pathway. J Med Chem. 2010 Dec 9;53(23):8260-73.