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product name NSC207895


Description: NSC 207895 suppresses MDMX with IC50 of 2.5 μM, leading to enhanced p53 stabilization/activation and DNA damage, and also regulates MDM2, an E3 ligase. NSC 207895 is a benzofuroxan derivative and is less toxic. NSC 207895 decreases the activity of MDMX promoter and subsequently decreases both the mRNA and protein levels of MDMX in MCF-7 cells. This inhibition of MDMX is accompanied with the activation of p53. 

Reference: Mol Cancer Ther. 2011 Jan;10(1):69-79.



Molecular Weight (MW)

279.25
Formula

C11H13N5O4
CAS No.

58131-57-0
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 0.4 mg/mL (1.43 mM)
Water: <1 mg/mL (slightly soluble or insoluble)
Ethanol: <1 mg/mL
Solubility (In vivo)

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19413412

NSC-207895 decreases both the MDMX mRNA and protein in MCF-7 cells. NSC-207895 induces expression of p53 as well as well-characterized p53-target gene, p21 and MDM2, in a dose-dependent manner in MCF-7 cells. NSC-207895 extends the half-life of p53 from 20 to 30 minutes to more than 3 hours as revealed by cycloheximide chase assays in MCF-7 cells.

In vivo  
Formulation  
Dosages  
Administration  
Reference [1] Wang H, et al. Mol Cancer Ther, 2011, 10(1), 69-79.

PAK4-IN-2