Journal of Chemical Information and Modeling · 2016 · 55 citations · 78 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryPharmacophore ModelingEnzyme InhibitionLigand-based DesignPharmacophore ScreeningPharmacophore-based Lead DiscoveryStructure-activity Relationship AnalysisVirtual ScreeningChemical Scaffold AnalysisEpoxide Hydrolase ActivityHit RateInhibitor ScreeningMedicinal Chemistry ApplicationsPharmacophore Model ConstructionPharmacophore-based Database SearchingPharmacophore-based Hit Identification
There is an increasing interest in the development of soluble epoxide hydrolase (sEH) inhibitors, which block the degradation of endogenous anti-inflammatory epoxyeicosatrienoic acids. Within this study, a set of pharmacophore models for sEH inhibitors was developed. The Specs database was virtually screened and a cell-free sEH activity assay was used for the biological investigation of virtual hits. In total, out of 48 tested compounds, 19 were sEH inhibitors with IC50 < 10 μM, representing a prospective true positive hit rate of 40%. Six of these compounds displayed IC50 values in the low nanomolar range. The most potent compound 21, a urea derivative, inhibited sEH with an IC50 = 4.2 nM. The applied approach also enabled the identification of diverse chemical scaffolds, e.g. the pyrimidinone derivative 29 (IC50 = 277 nM). The generated pharmacophore model set therefore represents a valuable tool for the selection of compounds for biological testing.
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Helen M. Berman · Nucleic Acids Research · 2000 · 39.8K citations
Paul C. D. Hawkins, A. Geoffrey Skillman, Gregory L. Warren et al. · Journal of Chemical Information and Modeling · 2010 · 1.7K citations · Full text