Publication | Open Access

Exploiting differences in caspase-2 and -3 S2 subsites for selectivity: Structure-based design, solid-phase synthesis and in vitro activity of novel substrate-based caspase-2 inhibitors

Medicinal Chemistry-3 S2 SubsitesSolid-phase SynthesisBiochemistryNatural SciencesMedicineStructure-based DesignNon-peptide LigandChemical BiologyPharmacologyPharmaceutical ChemistryDrug Discovery