kyp-2047 and Neuroblastoma

We have investigated the effect of regiospecifically introducing substituents in the P2 part of the typical dipeptide derived basic structure of PREP inhibitors. This hitherto unexplored modification type can be used to improve target affinity, selectivity, and physicochemical parameters in drug discovery programs focusing on PREP inhibitors. Biochemical evaluation of the produced inhibitors identified several substituent types that significantly increase target affinity, thereby reducing the need for an electrophilic "warhead" functionality. Pronounced PREP specificity within the group of Clan SC proteases was generally observed. Omission of the P1 electrophilic function did not affect the overall binding mode of three representative compounds, as studied by X-ray crystallography, while the P2 substituents were demonstrated to be accommodated in a cavity of PREP that, to date, has not been probed by inhibitors. Finally, we report on results of selected inhibitors in a SH-SY5Y cellular model of synucleinopathy and demonstrate a significant antiaggregation effect on α-synuclein.

Topics: alpha-Synuclein; Apoptosis; Cell Membrane Permeability; Crystallography, X-Ray; Enzyme Inhibitors; Humans; Kinetics; Mitochondrial Proteins; Models, Molecular; Molecular Structure; Neuroblastoma; Protein Multimerization; Pyrrolidines; Serine Endopeptidases; Structure-Activity Relationship; Substrate Specificity; Tumor Cells, Cultured