Publication | Open Access

One-pot, multi-component synthesis and structure-activity relationships of peptoid-based histone deacetylase (HDAC) inhibitors targeting malaria parasites

Drug TargetBiochemistryAntiparasitic AgentMedicineNatural SciencesPeptoidRational Drug DesignStructure-activity RelationshipsMulti-component SynthesisChemical BiologyPharmacologyPeptoid-based Histone DeacetylaseDrug Discovery