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JSH-23
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。
JSH-23图片
CAS NO:749886-87-1
规格:98%
分子量:240.34
包装与价格:
包装价格(元)
5mg询价
25mg询价
500mg询价
1g询价

NF-κB inhibitor
CAS:749886-87-1
分子式:C16H20N2
分子量:240.34
纯度:98%
存储:Store at -20°C

Background:

JSH-23 is an inhibitor of NF-κB transcriptional activity with IC50 value of 7.1μM [1].


JSH-23 is developed to inhibit NF-κB transcriptional activity in LPS-stimulated macrophages RAW 264.7. It shows a dose-dependent inhibition. This effect is not due to its cytotoxicity. In the same condition, JSH-23 is found to significantly decrease the LPS-induced DNA binding activity of NF-κB while decrease nuclear amount of NF-κB p65. JSH-23 plays these roles without affecting IκB degradation. In addition, JSH-23 also shows inhibition effects on the expression of the pro-inflammatory transcripts and enzymes, including IL-6, IL-1β, COX-2 and TNF-α. Furthermore, JSH-23 inhibits LPS-induced apoptotic chromatin condensation [1].


参考文献:
[1] Shin HM, Kim MH, Kim BH, Jung SH, Kim YS, Park HJ, Hong JT, Min KR, Kim Y. Inhibitory action of novel aromatic diamine compound on lipopolysaccharide-induced nuclear translocation of NF-kappaB without affecting IkappaB degradation. FEBS Lett. 2004 Jul 30;571(1-3):50-4.


 
 
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