Publication | Open Access

Discovery of structurally-diverse inhibitor scaffolds by high-throughput screening of a fragment library with dimethylarginine dimethylaminohydrolase

Targeted LibraryMedicinal ChemistryDrug TargetBioorganic ChemistryBiochemistryFragment LibraryNatural SciencesMedicineRational Drug DesignMolecular BiologyStructurally-diverse Inhibitor ScaffoldsDimethylarginine DimethylaminohydrolaseChemical BiologyMolecular DockingSmall Molecule LibraryDrug Discovery