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Cyclin-Dependent Kinases Inhibitor
No.167(October 2015)
![Kenpaullon](/assets/cms-images/K0052-1.gif)
Kenpaullon (1) is a cell-permeable inhibitor of several cyclin-dependent kinases, CDK1/cyclin B, CDK2/cyclin A, CDK2/cyclin E and CDK5/p35, as shown in the Table.1) 1 also inhibits GSK3β.1,2)
1 is also utilized for establishing induced pluripotent stem cells (iPSCs) as one of the chemical “substitutes” of Klf4, which is one of four transcription factors (Oct4, Klf4, Sox2, and c-Myc).3)
ALS (amyotrophic lateral sclerosis) is a neurodegenerative disease caused by motor neuron death. Rubin et al. found that 1 promoted the survival of motor neurons by using human ALS iPSCs and ES Cells derived from an ALS model mouse.4)
Table. Inhibition of selected protein kinases by kenpaullone1)
![Table. Inhibition of selected protein kinases by kenpaullone](/assets/cms-images/K0052-table.gif)
This product is for research purpose only.
References
- 1)Discovery and initial characterization of the paullones, a novel class of small-molecule inhibitors of cyclin-dependent kinases
- 2)The specificities of protein kinase inhibitors: An update
- 3)Reprogramming of murine fibroblasts to induced pluripotent stem cells with chemical complementation of Klf4
- 4)A small molecule screen in stem-cell-derived motor neurons identifies a kinase inhibitor as a candidate therapeutic for ALS
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