SJ 172550
Chemical Name: 2-[2-Chloro-4-[(1,5-dihydro-3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-ylidene)methyl]-6-ethoxyphenoxy]acetic acid methyl ester
Purity: ≥99%
Biological Activity
MDMX inhibitor. Reversibly binds MDMX (EC50 = 2.3 μM). Inhibits the MDMX-p53 interaction in cultured retinoblastoma cells; frees p53 to induce apoptosis.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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IGF1R as a Key Target in High Risk, Metastatic Medulloblastoma
Matthew N Svalina
Sci Rep, 2016;6(0):27012. -
Calpain-mediated degradation of MDMx/MDM4 contributes to HIV-induced neuronal damage.
Colacurcio D, Yeager A, Kolson D, Jordan-Sciutto K, Akay C
Mol Cell Neurosci, 2013;57(0):54-62. -
Identification and characterization of the first small molecule inhibitor of MDMX.
Reed et al.
J.Biol.Chem., 2010;285:10786
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