Title of article :
The role of molecular size in ligand efficiency
Author/Authors :
Charles H. Reynolds، نويسنده , , Scott D. Bembenek، نويسنده , , Brett A. Tounge، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Abstract :
Ligand efficiency is a simple metric for assessing whether a ligand derives its potency from optimal fit with the protein target or simply by virtue of making many contacts. Comparison of protein–ligand binding affinities for over 8000 ligands with 28 protein targets shows conclusively that the average ligand binding affinities are not linear with molecular size. It is therefore important to scale ligand efficiencies by the size of the ligand, particularly where small ligands (e.g., fragments) are involved. We propose a simple ‘fit quality’ metric that removes this dependence.
Keywords :
Fragment based design , Binding affinity , Ligand efficiency
Journal title :
Bioorganic & Medicinal Chemistry Letters
Journal title :
Bioorganic & Medicinal Chemistry Letters