Biophysical assay involves cleaving a quenched fluoregenic substrate that results in increased fluorescence. Difference between racemic mixture and pure components came to be ten times different in terms of IC50!
I'm assuming that you are asking about inhibitors of an enzyme. If the mixture of enantiomers is truly racemic (50:50), then the maximal differential potency between the racemic mixture and the more active of the purified enantiomers is 2-fold, since the racemic mixture is 50% active enantiomer. The differential between the more active and less active enantiomer can be much larger, since one enantiomer can, in principle, be completely inactive.