Not available outside of the UK & Ireland.
Biochem/physiol Actions
Target IC50: 3-6 µM against PKCδ; 5.3 µM against CaM kinase III
Reversible: yes
Product does not compete with ATP.
Primary TargetPKCδ
Cell permeable: yes
General description
A cell-permeable and reversible protein kinase C inhibitor that exhibits greater selectivity for PKCδ (IC50 = 3-6 µM) and PKCθ. Inhibits the PKCα, PKCβ, and PKCγ isoforms, but with significantly reduced potency (IC50 = 30-42 µM). Has reduced inhibitory activity on PKCε, PKCη, and PKCζ (IC50 = 80-100 µM). Also known to inhibit CaM kinase III (IC50 = 5.3 µM).
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes
Villalba, M., et al. 1999. J. Immunol. 163, 5813.Gschwendt, M., et al. 1994. Biochem. Biophys. Res. Commun. 199, 93.Gschwendt, M., et al. 1994. FEBS Lett.338, 85.Gschwendt, M., et al. 1984. Cancer Lett.25, 177.
Packaging
10 mg in Plastic ampoule
Reconstitution
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Warning
Toxicity: Standard Handling (A)
This product has met the following criteria to qualify for the following awards: