Chemical and Pharmaceutical Bulletin · 2013 · 10 citations · 2 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsEnzyme InhibitionLigand BindingPotency OptimizationProtein ChemistryStructure-activity Relationship AnalysisTyrosine Kinase InhibitorsBenzothiazole SynthesisCalcium-dependent Protein Kinase IiCalmodulin-dependent Protein Kinase IiIndole ChemistryKinase Inhibitor Library DesignKinase InhibitorsMedicinal Chemistry ApplicationsType Ii Kinase Inhibitors
Based on the structure activity relationship of 2-(4-phenoxybenzoyl)-5-hydroxyindole (1), a novel structural class of Ca²⁺/calmodulin-dependent protein kinase II (CaMKII) inhibitors were synthesized. We show in this study that the acidic proton at the N(1)-position of the indole moiety is not essential for CaMKII inhibitory activity. Among the synthesized compounds, we found the benzofuran and benzothiazole derivative as promising scaffolds for the developement of potent CaMKII inhibitors. In particular, compounds 8 and 14 inhibited CaMKII with IC₅₀ values of 24 nM and 32 nM, respectively.
2
Calmodulin Trapping by Calcium-Calmodulin-Dependent Protein Kinase
Tobias Meyer, Phyllis I. Hanson, Lubert Stryer et al. · Science · 1992 · 643 citations