Multidimensional De Novo Design Reveals 5-HT2B Receptor-Selective Ligands†
Dr. Tiago Rodrigues
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
These authors contributed equally to this work.
Search for more papers by this authorNadine Hauser
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
These authors contributed equally to this work.
Search for more papers by this authorDaniel Reker
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
Search for more papers by this authorDr. Michael Reutlinger
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
Search for more papers by this authorTiffany Wunderlin
Novartis Institutes for BioMedical Research (NIBR), Novartis AG, 4056 Basel (Switzerland)
Search for more papers by this authorDr. Jacques Hamon
Novartis Institutes for BioMedical Research (NIBR), Novartis AG, 4056 Basel (Switzerland)
Search for more papers by this authorDr. Guido Koch
Novartis Institutes for BioMedical Research (NIBR), Novartis AG, 4056 Basel (Switzerland)
Search for more papers by this authorCorresponding Author
Prof. Dr. Gisbert Schneider
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)Search for more papers by this authorDr. Tiago Rodrigues
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
These authors contributed equally to this work.
Search for more papers by this authorNadine Hauser
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
These authors contributed equally to this work.
Search for more papers by this authorDaniel Reker
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
Search for more papers by this authorDr. Michael Reutlinger
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
Search for more papers by this authorTiffany Wunderlin
Novartis Institutes for BioMedical Research (NIBR), Novartis AG, 4056 Basel (Switzerland)
Search for more papers by this authorDr. Jacques Hamon
Novartis Institutes for BioMedical Research (NIBR), Novartis AG, 4056 Basel (Switzerland)
Search for more papers by this authorDr. Guido Koch
Novartis Institutes for BioMedical Research (NIBR), Novartis AG, 4056 Basel (Switzerland)
Search for more papers by this authorCorresponding Author
Prof. Dr. Gisbert Schneider
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH), Vladimir-Prelog-Weg 4, 8093 Zurich (Switzerland)Search for more papers by this authorN.H. and T.R. performed organic syntheses. D.R. and M.R. contributed computational tools and performed in silico experiments together with N.H. and T.R. T.W., J.H., and G.K. contributed binding assays. All authors analyzed and discussed data. T.R. and G.S. designed the study and wrote the manuscript with feedback from the remaining authors.
Abstract
We report a multi-objective de novo design study driven by synthetic tractability and aimed at the prioritization of computer-generated 5-HT2B receptor ligands with accurately predicted target-binding affinities. Relying on quantitative bioactivity models we designed and synthesized structurally novel, selective, nanomolar, and ligand-efficient 5-HT2B modulators with sustained cell-based effects. Our results suggest that seamless amalgamation of computational activity prediction and molecular design with microfluidics-assisted synthesis enables the swift generation of small molecules with the desired polypharmacology.
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