Journal of Medicinal Chemistry · 2005 · 84 citations · 3 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsEnzyme InhibitionLead Compound DesignStructure-activity Relationship AnalysisBiological Evaluation ReportChemical Synthesis Of AnaloguesCore Scaffold LibrariesLead ScaffoldsMorpholine ChemistryQuinoline ChemistryQuinoline Synthesis
Synthesis, biological evaluation, and SAR dependencies for a series of novel 1,3-dioxo-2,3-dihydro-1H-pyrrolo[3,4-c]quinoline inhibitors of caspase-3 are described. The inhibitory activity of the synthesized compounds is highly dependent on the nature of 4-substituents on the core scaffold. 4-methyl-and 4-phenyl-substituted derivatives, which were the most active compounds within this series, inhibited caspase-3 with IC50 of 23 and 27 nM, respectively.
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Iraj Ganjian, Maliheh Khorshidi, I. Lalezari · Journal of Heterocyclic Chemistry · 1991 · 17 citations