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SC-26196 inhibited the desaturation of 2 microM [1-14C] 18:2n-6 by 87-95% in cultured human skin fibroblasts
2-(HETERO)ARYL-SUBSTITUTED ACETAMIDES FOR USE AS WNT SIGNALING MODULATORS
LBQ657 modestly inhibits cardiac myocyte hypertrophy
The plasma clearance is high at 3
Formula: C17H17F2NO2
MK 2206 Size:Solid 10 mg SC-26196 inhibited the desaturation ofMK2206 is a Akt inhibitor, is also an orally bioavailable allosteric inhibitor of the serine threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity. Akt inhibitor MK2206 binds to and inhibits the activity of Akt in a non ATP competitive manner, which may result in the inhibition of the PI3K Akt signaling pathway and tumor cell proliferation and the induction of tumor cell apoptosis. Product information CAS Number:
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