Publication | Open Access
<i>In </i><i>S</i><i>ilico</i>-Guided Target Identification of a Scaffold-Focused Library: 1,3,5-Triazepan-2,6-diones as Novel Phospholipase A2 Inhibitors
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2006
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Drug TargetPharmacotherapyHuman Spla2 MembersPharmaceutical ChemistryTarget IdentificationMolecular PharmacologyMedicinal ChemistryProteomicsBiochemistryMedicineMechanism Of ActionScaffold-focused LibraryDrug DevelopmentRepresentative MoleculesDruggable Active SitesPharmacologyNatural SciencesPeptide LibraryRational Drug DesignProtein EngineeringMolecular DockingDrug DiscoveryHigh-throughput Screening
A collection of 2150 druggable active sites from the Protein Data Bank was screened by high-throughput docking to identify putative targets for five representative molecules of a combinatorial library sharing a 1,3,5-triazepan-2,6-dione scaffold. Five targets were prioritized for experimental evaluation by computing enrichment in individual protein entries among the top 2% scoring targets. Out of the five proposed proteins, secreted phospholipase A2 (sPLA2) was shown to be a true target for a panel of 1,3,5-triazepan-2,6-diones which exhibited micromolar affinities toward two human sPLA2 members.
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