Inhibition of γ-secretase by the CK1 inhibitor IC261 does not depend on CK1δ

Bioorganic & Medicinal Chemistry Letters
2010.0

Abstract

CK1 and gamma-secretase are interesting targets for therapeutic intervention in the treatment of cancer and Alzheimer's disease. The CK1 inhibitor IC261 was reported to inhibit gamma-secretase activity. The question is: Does CK1 inhibition directly influence gamma-secretase activity? Therefore we analyzed the SAR of 15 analogues and their impact on gamma-secretase activity. The most active compounds were investigated on CK1delta activity. These findings exclude a direct influence of CK1delta on gamma-secretase, because any change in the substitution pattern of IC261 diminished CK1 inhibition, whereas gamma-secretase inhibition is still exerted by several analogues.

Knowledge Graph

Similar Paper

Inhibition of γ-secretase by the CK1 inhibitor IC261 does not depend on CK1δ
Bioorganic & Medicinal Chemistry Letters 2010.0
Modification of a promiscuous inhibitor shifts the inhibition from γ-secretase to FLT-3
Bioorganic & Medicinal Chemistry Letters 2012.0
Synthesis and structure–activity relationship of a novel series of heterocyclic sulfonamide γ-secretase inhibitors
Bioorganic & Medicinal Chemistry 2009.0
Roscovitine-Derived, Dual-Specificity Inhibitors of Cyclin-Dependent Kinases and Casein Kinases 1
Journal of Medicinal Chemistry 2008.0
Development of dual casein kinase 1δ/1ε (CK1δ/ε) inhibitors for treatment of breast cancer
Bioorganic & Medicinal Chemistry 2018.0
SAR studies of acidic dual γ-secretase/PPARγ modulators
Bioorganic & Medicinal Chemistry 2011.0
Design, Synthesis, and Biological Evaluation of a Novel Class of γ-Secretase Modulators with PPARγ Activity
Journal of Medicinal Chemistry 2010.0
New Dual CK2/HDAC1 Inhibitors with Nanomolar Inhibitory Activity against Both Enzymes
ACS Medicinal Chemistry Letters 2020.0
Synthesis and evaluation of new potent inhibitors of CK1 and CDK5, two kinases involved in Alzheimer’s disease
Medicinal Chemistry Research 2013.0
Discovery of (R)-4-Cyclopropyl-7,8-difluoro-5-(4-(trifluoromethyl)phenylsulfonyl)-4,5-dihydro-1H-pyrazolo[4,3-c]quinoline (ELND006) and (R)-4-Cyclopropyl-8-fluoro-5-(6-(trifluoromethyl)pyridin-3-ylsulfonyl)-4,5-dihydro-2H-pyrazolo[4,3-c]quinoline (ELND007): Metabolically Stable γ-Secretase Inhibitors that Selectively Inhibit the Production of Amyloid-β over Notch
Journal of Medicinal Chemistry 2013.0