Biochem/physiol Actions
Target IC50: 625 nM and ﹤1.25 µM in blocking Akt-mediated FOXO1a nuclear export and cell proliferation, respectively, in 786-O cells
Reversible: yes
Product does not compete with ATP.
Primary TargetAkt
Cell permeable: yes
General description
A cell-permeable benzimidazole compound that inhibits Akt phosphorylation/activation presumably by targeting the ATP binding site of a kinase upstream of Akt, but downstream of PI3K. Shown to block Akt-mediated FOXO1a nuclear export (IC50﹤/sub> = 625 nM) and cell proliferation (IC50﹤/sub><1.25 µM) in 786-O cells. Unlike phosphatidylinositol analog-based Akt inhibitors (Cat. Nos. 124005, 124008, 124009), this inhibitor does not affect PI3K.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Packaging
1 mg in Plastic ampoule
Packaged under inert gas
Please refer to vial label for lot-specific concentration.
Physical form
A 10 mM (1 mg/163 µl) solution of Akt Inhibitor IV (Cat. No. 124011) in DMSO.
Reconstitution
Following initial use, aliquot and refrigerate (4°C).
Warning
Toxicity: Irritant (B)
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