This
analysis elucidates the impact of small molecule architecture
on common in vitro ADME assays. In vitro parameters considered in
this analysis included Caco-2 permeability/efflux, CYP3A4 inhibition,
hERG inhibition, and rat microsomal extraction ratio (ER). The statistical
significance and practical meaningfulness of chirality were determined
by comparison of the distribution of enantiomers with the experimental
variation distribution observed from duplicate measurements. Statistical
tools were applied to characterize the role of molecular architecture
on the outcome of a given in vitro assay. We found that CYP3A4 inhibition,
hERG inhibition, Caco-2 permeability, and efflux are unlikely to be
modulated by chirality. However, rat microsomal ER provides a statistically
significant, <i>and quantitatively meaningful</i>, chance
of being influenced by chirality