Inhibiteur JNK VIII

Code: 420135-5MG D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Biochem/physiol Actions

Reversible: yes

Product competes with ATP.

Target Ki: 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively

Cell permeable...


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$300.20 EACH

Non disponible en dehors du Royaume-Uni et de l'Irlande

Biochem/physiol Actions

Reversible: yes

Product competes with ATP.

Target Ki: 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively

Cell permeable: yes

General description

A cell-permeable pyridinylamide compound that acts as an ATP-competitive, reversible inhibitor of JNK (Ki = 2 nM, 4 nM and 52 nM for JNK1, 2 and 3, respectively) and displays excellent selectivity over 72 other kinases. Inhibits c-jun phosphorylation with an EC50 of 920 nM in HepG2 cells. Preferentially blocks the growth of PTEN null mouse embryonic fibroblasts.

Legal Information

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

Other Notes

Vivanco, I., et al. 2007. Cancer Cell11, 555.Szczepankiewicz, B. G., et al. 2006. J. Med. Chem.49, 3563.

Packaging

Packaged under inert gas

5 mg in Plastic ampoule

Warning

Toxicity: Standard Handling (A)

assay≥95% (HPLC)
colorbrown
formsolid
manufacturer/tradenameCalbiochem®
Quality Level100
shipped inambient
solubilityDMSO: 10 mg/mL
storage conditionprotect from light, OK to freeze
storage temp.−20°C
Cas Number894804-07-0
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :



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