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BI-D1870

Catalog No.GC13468

Le BI-D1870 est un inhibiteur compétitif pour l'ATP, perméable aux cellules et pénétrant dans le cerveau des isoformes RSK, avec des IC50 de 31 nM/24 nM/18 nM/15 nM pour RSK1/RSK2/RSK3/RSK4, respectivement.

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BI-D1870 Chemical Structure

Cas No.: 501437-28-1

Taille Prix Stock Qté
10mM (in 1mL DMSO)
119,00 $US
En stock
5mg
83,00 $US
En stock
10mg
128,00 $US
En stock
50mg
333,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

BI-D1870 is a cell-permeable inhibitor of the p90 RSK isoforms with IC50 values of 31nM, 24nM, 18nM and 15nM for RSK1, RSK2, RSK3 and RSK4 respectively [1].

BI-D1870 is a derivative of dihydropteridinone and found to be a remarkably specific inhibitor of RSK isoforms. It is an ATP-competitive inhibitor. When the concentrations of ATP are 10μM and 100μM, the IC50 values of BI-D1870 against RSK1 and RSK2 are 5nM, 10nM and 10nM, 20nM, respectively. BI-D1870 also inhibits RSK3 and RSK4 with IC50 values of 18nM and 15nM respectively, when ATP is 100μM. The inhibition activity of BI-D1870 against RSK is more than 500-fold greater than some other AGC kinases suggesting BI-D1870 as a specific inhibitor of RSK. In addition, BI-D1870 is reported to induce the phosphorylation of ERK1/ERK2 and the subsequent phosphorylation of CREB in Rat-2 cells [1].

References:
[1] Sapkota G, Cummings L, Newell F, et al. BI-D1870 is a specific inhibitor of the p90 RSK (ribosomal S6 kinase) isoforms in vitro and in vivo. Biochem. J, 2007, 401: 29-38.

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