Nur77-p38 Interaction Inhibitor, PDNPA,10MG,5382410001,Sigma

销售价: ¥ 2240.80 / 件
在线询价
优    惠: 请询价
订货号 0BW0523
品牌型号 Sigma 5382410001
货期 询货期
最小订货量 1件
联系我们
  • 400-920-3909
微信扫一扫,手机采购
  • 商品介绍
  • 规格参数
  • 包装参数
产品介绍 Product Description

General description

A cell-permeable phenylacetate based compound that specifically blocks the Nur77-p38α interaction by directly targeting the ligand-binding domain of Nur77 (~1 to 10 µM) and impedes Nur77 phosphorylation by p38α. Does neither modulate p38α kinase activity nor affects the stability of the p38α-Nur77 complex. Inhibits p65 binding to DNA and blocks LPS-induced (100 ng/ml) NF-κB activity in RAW264.7 cells (IC50 = 1.6 µM), but does not affect the interaction between Nur77 and p65. Shown to reduce IL-6 concentration and prolong the lifespan of wild type mice treated with LPS. Also increases the survival rate of wild-type mice subjected to cecal ligation and puncture (CLP)-induced sepsis.

Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water.


Biochem/physiol Actions

Cell permeable: yes
Primary Target
Nur77
Reversible: yes


Packaging

Packaged under inert gas


Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.


Other Notes

Li, L., et al. 2015. Nat. Chem. Biol.11, 339.


Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany


Disclaimer

Toxicity: Standard Handling (A)


技术参数 Specifications
assay≥97% (HPLC)
Quality Segment100
formsolid
potency1.6 μM IC50
manufacturer/tradenameCalbiochem®
storage conditionOK to freeze,protect from light
color white
solubilityDMSO: 100 mg/mL
storage temp.−20°C
长度(mm)
宽度(mm)
高度(mm)
重量(kg)
猜你喜欢

在线
客服

在线客服服务时间:09:00-18:00

微信扫码咨询

客服
热线

400-920-3909
客服服务热线 周一至周五(09:00-18:00)

微信
咨询

微信小程序 7X24小时在线咨询