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402081  Indirubin Derivative E804

IDR E804

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25 May 2012

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402081-1MG  1 mg 
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A cell-permeable indirubin derivative (IDR) that blocks the Src-Stat3 signaling pathway and displays anti-tumor properties. Shown to be a potent, reversible, and ATP-competitive inhibitor of the kinase activities of Src (IC50 = 430 nM), Cdk1/cyclin E (IC50 = 210 nM), Cdk2/cyclin A (IC50 = 540 nM), and Cdk1/cyclin B (IC50 = 1.65 µM). Reduces the tyrosine phosphorylation levels of Src, JAK1, and Stat3 in MDA-MB-468 cells in a time- and dose-dependent manner. Selectively induces apoptosis in cells expressing high levels of active Stat3, but not cells lacking activated Stat3. The apoptotic effect of E804 is shown to be due to the down-regulation of antiapoptotic proteins Mcl-1 and survivin.
Product information
Form Dark red solid
Primary Target Src
Primary Target IC50 430 nM
Secondary target Cdk1/cyclin E (IC50 = 210 nM), Cdk2/cyclin A (IC50 = 540 nM), and Cdk1/cyclin B (IC50 = 1.65 µM)
Molar mass 365.4
Protect from Light Yes
Packaged under inert gas Yes
Cell permeable Yes
ATP Competitive Yes
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C20H19N3O4
CAS number 854171-35-0
Store and ship information
Storage -20°C
Ship Shipped with Blue Ice or with Dry Ice
Standard Handling
Indirubin Derivative E804, molecular structure

© Merck KGaA, Darmstadt, Germany, 2012

All references to Merck refer to Merck KGaA, Darmstadt, Germany.


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