Journal of Medicinal Chemistry · 2015 · 64 citations · 32 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryEnzymologyChemical Library DesignEnzyme InhibitionLigand BindingMolecular Targets Of DrugsNucleic Acid Drug DesignPolymerase Chain ReactionAffinity ScreeningDna-encoded Library TechnologyEnzyme Inhibitor DiscoveryInhibitor ScreeningLigand-based ScreeningPoly Adp-ribose Polymerase InhibitorsPoly(adp-ribose) Polymerase InhibitorsSmall-molecule Library Design
We describe the synthesis and screening of a DNA-encoded chemical library containing 76230 compounds. In this library, sets of amines and carboxylic acids are directly linked producing encoded compounds with compact structures and drug-like properties. Affinity screening of this library yielded inhibitors of the potential pharmaceutical target tankyrase 1, a poly(ADP-ribose) polymerase. These compounds have drug-like characteristics, and the most potent hit compound (X066/Y469) inhibited tankyrase 1 with an IC50 value of 250 nM.
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