D 4476
Chemical Name: 4-[4-(2,3-Dihydro-1,4-benzodioxin-6-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]benzamide
Purity: ≥99%
Biological Activity
D 4476 is a selective inhibitor of casein kinase 1 (CK1) and TGF-β type-I receptor (ALK5) that displays > 20-fold selectivity over SAPK2/p38 and a much greater selectivity over all other protein kinases tested. Suppresses site-specific phosphorylation and nuclear exclusion of FOXO1a.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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The selectivity of protein kinase inhibitors: a further update.
Bain et al.
Biochem.J., 2007;408:297 -
D4476, a cell-permeant inhibitor of CK1, suppresses the site-specific phosphorylation and nuclear exclusion of FOXO1a.
Rena et al.
EMBO Rep., 2004;5:60 -
Identification of novel inhibitors of the transforming growth factor β1 (TGF-β1) type I receptor (ALK5).
Callahan et al.
J.Med.Chem., 2002;45:999
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Citations for D 4476
The citations listed below are publications that use Tocris products. Selected citations for D 4476 include:
5 Citations: Showing 1 - 5
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Mammalian FMRP S499 Is Phosphorylated by CK2 and Promotes Secondary Phosphorylation of FMRP.
Authors: Bartley Et al.
Eneuro 2016;3
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GSK3β-Dzip1-Rab8 cascade regulates ciliogenesis after mitosis.
Authors: Zhang Et al.
PLoS Biol 2015;13:e1002129
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CK1δ and CK1ε are components of human 40S subunit precursors required for cytoplasmic 40S maturation.
Authors: Zemp Et al.
J Cell Sci 2014;127:1242
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Pathogen recognition receptor signaling accelerates phosphorylation-dependent degradation of IFNAR1.
Authors: Qian Et al.
PLoS Pathog 2011;7:e1002065
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Perspectives on Regulatory T Cell Therapies.
Authors: Probst-Kepper Et al.
Toxins (Basel) 2009;36:302
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