Advanced modalities like PROTACs, molecular glues, and Antibody Drug Conjugates (ADCs) are redefining the boundaries of drug discovery.
Kinase drug discovery is complex due to conserved ATP binding pockets and high structural homology, making selectivity and mechanism of action assessment particularly challenging. To support rapid, confident decision making, Eurofins Discovery provides a comprehensive suite of kinase platforms that deliver high quality data across binding, activity, cellular context, and mechanistic profiling.
KINOMEscan uses a site directed competition binding assay to quantify interactions across over 500 kinase domain-containing wildtype and clinically relevant mutant targets. It supports multiple compound modalities (small molecules, peptides, conjugates, covalent inhibitors, and bifunctional degraders) and offers fast turnaround to maintain project momentum.
TREEspot® data visualization tool enables clear visualization of kinome-wide binding and efficient identification of differentiated selectivity profiles.
To complement binding data, KinaseProfiler measures functional activity across 450+ biologically relevant kinases using radiometric, luminescence, and TR FRET technologies. Researchers can select ATP conditions (10 µM, Km, or 1 mM) to model biological scenarios more accurately.
A guaranteed six business day turnaround supports rapid SAR cycles, hit validation, and early derisking of lead candidates.
Eurofins Discovery adds key layers of physiological and mechanistic insight:
These complementary tools help researchers move beyond simple inhibition measurements toward more complete pharmacological profiling.
Eurofins Discovery’s kinase solutions are designed for efficiency and clarity:
This combination of scientific depth and operational reliability supports an experience where researchers learn more and progress faster.
Discover our Kinase solutions here:
https://apac.eurofinsdiscovery.com/solution/kinases
