Improving drug quality
We characterize the kinetic profile of your drugs to boost their clinical efficacy
The efficacy of target inhibition depends on the rate constant of both the association and dissociation of a drug molecule to and from the target. The onset of the drug action is influenced by the association rate: the faster a drug binds to the target, the faster the inactivation will occur. Conversely, the duration of drug action is dependent of the dissociation rate: the longer the duration of binding, the longer the pharmacodynamic effect.
We use a fast and simple method to measure the affinity constant (Kd), the association rate constant (kon), the dissociation rate constant (koff) and the residence time of your compounds.
Features & benefits:
- Identification of compounds with the desired kinetic parameters as an efficient starting point for lead development
- Parallel optimization of binding affinity and binding kinetics
- Evaluation of both active and inactive kinases
- Rapid turnaround time
- Accurate and reproducible data
See application note.
Kinase target list:
View by kinase target
View by kinase group
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