Description
GSK-2334470 is a selective inhibitor of PDK1 that exhibits anticancer activity in in vitro models. GSK-2334470 inhibits T-loop phosphorylation of SGK and S6K1, Akt and Akt substrates GSK3, FoxO, and PRAS40, and ERK substrate RSK2.
Product Unit Size | Cost | Quantity | Stock |
---|
GSK-2334470 is a selective inhibitor of PDK1 that exhibits anticancer activity in in vitro models. GSK-2334470 inhibits T-loop phosphorylation of SGK and S6K1, Akt and Akt substrates GSK3, FoxO, and PRAS40, and ERK substrate RSK2.
Cas No. | 1227911-45-6 |
---|---|
Purity | ≥99%, ≥99%ee |
Formula | C25H34N8O |
Formula Wt. | 462.59 |
Chemical Name | (3S,6R)-1-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)pyrimidin-4-yl]-N-cyclohexyl-6-methylpiperidine-3-carboxamide |
IUPAC Name | (3S,6R)-1-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)pyrimidin-4-yl]-N- cyclohexyl-6-methylpiperidine-3-carboxamide |
Solubility | DMSO 28 mg/mL (64.6 mM) Water Insoluble Ethanol Insoluble |
Appearance | off-white powder |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Najafov A, Sommer EM, Axten JM, et al. Characterization of GSK2334470, a novel and highly specific inhibitor of PDK1. Biochem J. 2011 Jan 15;433(2):357-69. PMID: 21087210.
Nucleoside (deoxycytidine) analog; DNMT inhibit...
mTORC1 inhibitor.
Endogenous peptide hormone, involved in secreti...
Organosulfur found in cruciferous vegetables; a...
Coccidiostat; dihydrofolate reductase inhibitor...
Synthetic taxol synthesis intermediate; microtu...
μOR and δOR agonist, D2/D3 DA potentiator.
c-Raf inhibitor.
Non-nitrogen bisphosphonate; mitochondrial ATP/...
Methoxy aminopropyl carbazole, neuroprotective....
GABA-A α5/3/2 positive modulator.
Glycoside hydroquinone originally found in Berg...
Endogenous cardiomodulatory peptide; NPR-B agon...
Viral M2 proton channel blocker.
Synthetic type II pyrethroid insecticide; prote...
Akt inhibitor.
ET-A/B antagonist.
T-type Ca2+ and voltage-gated Na+ channel block...
D2/3 antagonist, hERG K+ channel blocker.
Naphthalene; indirect STAT1 agonist.