Overview MDL MFCD12828759 Molecular Weight 410.32 Molecular Formula C19H22Cl2FN5 SMILES NC=1N=C(C2=C(N=CN2C3CCCCC3)C4=CC=C(F)C=C4)C=CN1.Cl
For research use only.
Storage 3 years,-20°C,powder 1 years,-80°C,in solvent
Shipping Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)
Preparing Stock Solutions Concentration Volume Mass 1 mg 5 mg 10 mg 1 mM 2.4371 mL 12.1856 mL 24.3712 mL 5 mM 0.4874 mL 2.4371 mL 4.8742 mL 10 mM 0.2437 mL 1.2186 mL 2.4371 mL 50 mM 0.0487 mL 0.2437 mL 0.4874 mL
Description PF-670462 is a potent and selective inhibitor of and with IC50 value of 90 nM and 13 nM, respectively.
Targets CK1δ [1] (Cell-free assay) CK1ε [1] (Cell-free assay) 13 nM 90 nM
In vitro PF-670462 is a 14 nM inhibitor of CK1δ in vitro and also potently inhibits p38 and EGFR. In vitro, PF670462 prevents TGF-β-induced epithelial-mesenchymal transition.
Synonyms 2-Pyrimidinamine, 4-[1-cyclohexyl-4-(4-fluorophenyl)-1H -imidazol-5-yl]-, hydrochloride (1:2)
PF 670462