I did my master in Analytical chemistry, and My project was about 3D-QSAR on a series of cdk5/p25 inhibitors using 3D-QSAR and Docking.
Three-dimensional quantitative structure-activity relationship (3D-QSAR) techniques are useful methods of ligand-based drug design by correlating physicochemical descriptors from a set of related compounds to their known molecular activity or molecular property values.