An evaluation of a variety of structure-based clustering methods for use in compound selection is presented. The use of MACCS, Unity and Daylight 2D descriptors; Unity 3D rigid and flexible descriptors and two in-house 3D descriptors based on potential pharmacophore points, are considered. The use of Ward's and group-average hierarchical agglomerative, Guénoche hierarchical divisive, and Jarvis−Patrick nonhierarchical clustering methods are compared. The results suggest that 2D descriptors and hierarchical clustering methods are best at separating biologically active molecules from inactives, a prerequisite for a good compound selection method. In particular, the combination of MACCS descriptors and Ward's clustering was optimal.
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Brown et al. (1996) studied this question.
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