Journal of Medicinal Chemistry · 2001 · 42 citations · 11 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsDrug-receptor InteractionsLigand BindingLigand-based DesignReceptor PharmacologyReceptor-ligand InteractionsStructure-activity Relationship AnalysisGlucagon Receptor AgonismGlucagon Receptor AntagonismGlucagon Receptor PharmacologyPeptide Medicinal ChemistryPharmacological PotencyPharmacological ScreeningReceptor Binding OptimizationSmall-molecule Library Design
High throughput screening of our small molecule combinatorial library identified a class of benzoylnaphthalenehydrazones with modest affinity for the human glucagon receptor. Optimization of this initial hit through a series of targeted libraries and traditional medicinal chemistry led to ligands with nanomolar affinities. Pharmacological evaluation demonstrated that these ligands were competitive glucagon receptor antagonists. Intravenous administration of a representative benzoylnaphthalenehydrazone into rats attenuated glucagon-stimulated glucose levels.
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115th National Meeting American Chemical Society
Chemical & Engineering News · 1949 · 288 citations
Potent, orally absorbed glucagon receptor antagonists
Stephen E. de Laszlo, Candice Hacker, Bing Li et al. · Bioorganic & Medicinal Chemistry Letters · 1999 · 169 citations · Full text
Hyperglycemia of Diabetic Rats Decreased by a Glucagon Receptor Antagonist
David G. Johnson, Camy Ulichny Goebel, Victor J. Hruby et al. · Science · 1982 · 166 citations