Kenpaullone
GSK3Beta,CDK2 and LCK Inhibitor
Product Specifications
Background
Kenpaullone is a potent inhibitor of CK1 and CDK2, and slightly less on CDK5, by competitive inhibition of adenosine triphosphate (ATP) binding. It is also useful as an inhibitor of GSK3Beta.
Product Name Alternative
9-Bromo-7,12-dihydro-indolo[3,2-d][1]benzazepin-6(5H)-one; NSC-664704
UNSPSC
41116105
Source
Synthetic
Purity
>98% (HPLC); NMR (Conforms)
Weight
0.005
Format
Beige powder
Solubility
May be dissolved in DMSO (35 mg/ml)
Molecular Formula
C16H11BrN2O
Molecular Weight
327.2
Precautions
Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
References & Citations
1. https://www.sciencedirect.com/topics/pharmacology-toxicology-and-pharmaceutical-science/kenpaullone
CAS Number
142273-20-9
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