Synthesis of HDAC Substrate Peptidomimetic InhibitorsUsing Fmoc Amino Acids Incorporating Zinc-Binding Groups

摘要

Syntheses of Fmoc amino acids having zinc-binding groups were prepared and incorporated into substrate inhibitor H3K27 peptides using Fmoc/^tBu solid-phase peptide synthesis (SPPS). Peptide >11, prepared using Fmoc-Asu(NHO^tBu)-OH, is a potent inhibitor (IC50 = 390 nM) of the core NuRD corepressor complex (HDAC1–MTA1–RBBP4). The Fmoc amino acids have the potential to facilitate the rapid preparation of substrate peptidomimetic inhibitor (SPI) libraries in the search for selective HDAC inhibitors.