Kinases and phosphatases
Kinase inhibitors
For the study of the intimate cascades of signal transduction pathways new compounds are continuously introduced in our catalogue.
Kinase inhibitor specificity table

New Kinase Inhibitors
STA-21 is a novel Stat3-selective inhibitor. It inhibits Stat3 dimerization and DNA binding as well as Stat3-dependent luciferase reporter activity.
SC-514 is a selective and ATP-competitive inhibitor of IKK2 (IC50 = 11.2 µM). It does not inhibit other IKK isoforms or other serine/threonine or tyrosine kinases.
BML-259 is a potent inhibitor of Cdk5/p25 (IC50 = 64 nM). It also inhibits Cdk2 (IC50 = 98 nM).
Apigenin inhibits casein kinase 2. This inhibition decreases the rate of IκBα turnover and nuclear levels of NFκB in WEHI 231 murine B-lymphoma cell line.

New Kinase inhibitor library
The new Screen-Well™ kinase inhibitor library is a cheap and convenient ready-to-use tool for chemical genomics, assay development and other pharmacological applications. This library includes 80 known kinase inhibitors already dissolved in DMSO at 10 mM. They are aliquoted into deep-well plates at either 100 or 500 µl per well. Please contact us to receive the full list of inhibitors as well as compound structure files.
Product spotlight

NameSizeRef.Price (excl. VAT)
DEGUELIN
5 mgEI-329-000590.00 €
ML-9
10 mgEI-153-001060.00 €
Myelin Basic Protein
10 mgGLO126295.00 €
NSC-95397
5 mgEI-309-0005130.00 €
PRAS40
25 ugSE-308-0025280.00 €
SB-415286
1 mgEI311-000177.00 €
TRICIRIBINE
1 mgEI-332-0001170.00 €
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