Biochem/physiol Actions
Cell permeable: no
Reversible: no
Target IC50: 300 nM and 120 nM against diacylglycerol kinase in isolated platelet membranes and in intact platelets, respectively
Product does not compete with ATP.
General description
Inhibitor useful for elucidating roles of protein kinase C. Inhibits diacylglycerol (DAG) kinase in isolated platelet membranes (IC50 = 300 nM) and in intact platelets (IC50 = 120 nM). A more potent analog of DAG kinase inhibitor I.
Inhibits diacylglycerol kinase in isolated platelet membranes (IC50 = 300 nM) and in intact platelets (IC50 = 120 nM) by binding to the catalytic domain. A more potent analog of diacylglycerol kinase inhibitor I (Cat. No. 266785).
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes
Jiang, Y., et al. 2000. Biochem. Pharmacol. 59, 763.Jones, D.R., et al. 1999. J. Biol. Chem.274, 16846.Rodriguez-Linares, B., et al. 1991. Biochem. Pharmacol. 41, 835.de Chaffoy de Courcelles, D., et al. 1989. J. Biol. Chem.264, 3274.
Packaging
5 mg in Glass bottle
Reconstitution
Following reconstitution, aliquot, flush with an inert gas and freeze at -20°C. Stock solutions are stable for up to 6 months at -20°C.
Warning
Toxicity: Irritant (B)
Quantity
Est. Dispatch/Availability