Virtual Lead Selectivity Test

The Quantum Lead Selectivity Test explores the potential selectivity of a drug candidate, adverse activity and additional unexpected activity by screening it against thousands of proteins in silico.

Using our propriety computational technology, QUANTUM, we calculate the IC50 value quickly and accuarately in order to predict the activity of the drug candidate. The hit rate of QUANTUM is about 50%, which means that half of strong inhibitors found in silico will be confirmed in in-vitro testing!!! This service provides a web interface to select a set of proteins for screening purposes. The default profile contain approximately 1000 proteins. Click to access the Lead Selectivity Web Interface.

With the imperative to “fail fast, fail cheap”, our Lead selectivity testcan help you to make decisions regarding the further drug development pathway and strategy —which entities to pursue or which to withdraw.

Note that you can also purchase the Lead Selectivity Module, however; this module requires significant computational resources. For detailed information, please contact us.

Click to download the Lead Selectivity Module overview brochure

Quantum technology is applicable to any protein with a resolved 3D structure. You can search our catalogue for 3D structures or submit your own for compound profiling and selectivity screens.

You have accessed back-upped version of our site. Please reffer to new home page for a more up-to-date information.

Browse the catalogue using PDB ID starting with: