assay
≥98% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, desiccated (hygroscopic), protect from light
color
off-white
shipped in
ambient
Quality Level
General description
A cell-permeable tri-substituted imidazole compound that acts as a potent and reversible inhibitor of casein kinase Iε/δ (IC50 = 7.7 and 14 nM, respectively) with modest to excellent selectivity over EGFR and p38 MAPK (IC50 = 150 and 190 nM, respectively) and over 43 related kinases (IC50 >0.3 to 30 µM), and a panel containing 116-receptors, transporters and other enzymes. Shown to inhibit PER3 nuclear translocation in GFP-PER3 and CKIε-cotransfected COS7 cells (EC50 = 290 nM), and induce phase delays in circadian rhythms of monkeys & rats model (10 - 100 mg, s.c.); further, attenuate the locomotor stimulant response to methamphetamine.
Packaging
Packaged under inert gas
Preparation Note
Soluble in DMSO (<100 mM) or H2O ( <100 mM); aliquot & store at -20*C; stable for 6 months. Most likely to compete with ATP.
Other Notes
Bryant, C.D., et al. 2009. Psychopharmacology203, 703.
Sprouse, J., et al. 2009. Psychopharmacology204, 735.
Badura, L., et al. 2007. J. Pharmacol. Exp. Ther.322, 730.
Sprouse, J., et al. 2009. Psychopharmacology204, 735.
Badura, L., et al. 2007. J. Pharmacol. Exp. Ther.322, 730.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
存储类别
10-13 - German Storage Class 10 to 13
法规信息
监管及禁止进口产品
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