GSK2334470
Potent and selective PDK1 inhibitor / Potent (IC50 = 10 nM) and selective inhibitor of 3-Phosphoinositide-dependent kinase 1 (PDK1), which phosphorylates and activates a group of protein kinases in the AGC/PKG/PKC family.1 It is more effective at inhibiting PDK1 substrates that are activated in the cytosol rather than at the plasma membrane.1 GSK2334470 delayed melanogenesis and metastasis in Braf(V600E)::Pten(-/-) mice.2 It also displays antitumor activity against multiple myeloma synergistically with mTORC1/2 inhibitor PP2423 and proteasome inhibitor MG-1324.
Biochemicals & reagents
1227911-45-6
GSK-470
1) Najafov et al. (2011), Characterization of GSK2334470, a novel and highly specific inhibitor of PDK1; Biochem.J. 433 37 2) Scortegagna et al. (2014), Genetic inactivation or pharmacological inhibition of Pdk1 delays development and inhibits metastasis of Braf (V600E)::Pten(-/-) melanoma; Oncogene 33 4330 3) Yang et al. (2017),PDK1 inhibitor GSK2334470 exerts antitumor activity in multiple myeloma and forms a novel multitargeted combination with dual mTORC1/C2 inhibitor PP242; Oncotarget 8 39185 4) Zhang et al. (2018), PDK1 inhibitor GSK2334470 synergizes with proteasome inhibitor MG-132 in multiple myeloma cells by inhibiting full AKT activity and increasing nuclear accumulation of PTEN protein; Oncol.Rep. 39 2951
-20°C
TARGET: Kinase -- PATHWAY: Ferroptosis; AKT; Lipid signaling; ERK -- RESEARCH AREA: Cell death -- DISEASE AREA: Cancer