Skip to main content
Fig. 3 | Journal of Cheminformatics

Fig. 3

From: MolFinder: an evolutionary algorithm for the global optimization of molecular properties and the extensive exploration of chemical space using SMILES

Fig. 3

A comparison of modified drug-likeness scores of the generated molecules The violin plots of the modified drug-likeness scores of generated molecules by MolFinder, MolFinder-local, ReLeaSE, and MolDQN (top). The histogram of QED (left bottom) and SA score (right bottom) values of the generated molecules by MolFinder (orange), ReLeaSE (green), and MolDQN (red), and those of the initial ZINC15 database (blue)

Back to article page

Journal of Cheminformatics

ISSN: 1758-2946

Contact us