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526523  PIM1/2 Kinase Inhibitor V

(Z)-5-(3-Trifluoromethylbenzylidene)thiazolidine-2,4-dione, SMI-4a

A cell-permeable thiazolidinedione compound that acts as a potent, ATP-competitive inhibitor against Pim-1/2 kinases (IC50 = 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 32PO4 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 (IC50 = 17 vs. 48 µM with repsective inhibitor).
Product number Size Quantity Price / Availability
526523-5MG  5 mg 
USD 79.00  
Product information
Form Light beige solid
Molar mass 273.2
Protect from Light Yes
Packaged under inert gas Yes
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C11H6F3NO2S
Store and ship information
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
PIM1/2 Kinase Inhibitor V, molecular structure

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