

ab120600 · 5 mg
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Description
MW 383.8 Da, Purity >98 %. Cell-permeable, selective inhibitor of protein kinase C IC50 = 0.66 muM ; Competitive with respect to the phosphate acceptor and non-competitive with respect to ATP. Activates MAPK pathways, independent of PKC inhibition. Inhibits BclXL function IC50 = 1.5 muM by displacing Bax binding, inducing apoptosis in several cancer cell lines.






