A cell-permeable thiazolidinedione compound that acts as a potent, ATP-competitive inhibitor against Pim-1/2 kinases (IC
50 = 24 nM and 100 nM against Pim-1 and Pim-2, respectively), while exhibiting little or no activity against a panel of 58 other kinases (≤20% inhibition at 5 µM). One hour inhibitor treatment (0.5 µM) of HEK-293T cultures at the end of a 4 hour
32PO
4 incubation period results in nearly complete inhibition of the autophosphorylation of overexpressed Pim-1. Comparing to Inhibitor VI (Cat. No.
526524), Inhibitor V is less reactive towards DYRK1α (20% vs. 68% inhibition with repsective inhibitor at 5 µM) and more potent in PC3 human prostate cancer cell killing (IC
50 = 17 vs. 48 µM with repsective inhibitor).
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Product information
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Form
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Light beige solid
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Molar mass
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273.2
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Protect from Light
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Yes
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Packaged under inert gas
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Yes
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Purity
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≥95% by HPLC
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Solubility
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DMSO
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Chemical formula
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C11H6F3NO2S
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Store and ship information
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Storage
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+2°C to +8°C
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Ship
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Ambient Temperature Only
Standard Handling
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