GNE-6776

2009273-71-4

C20H20N4O2

DMSO : >= 310 mg/mL (889.78 mM)

Cell Cycle/DNA Damage

GNE-6776 is a selective USP7 inhibitor. IC50 & Target: USP7^[1] In Vitro: GNE-6776 non-covalently targets USP7 12?� distant from the catalytic cysteine. GNE-6776 attenuates ubiquitin binding and thus inhibits USP7 deubiquitinase activity. GNE-6776 interacts with acidic residues that mediate hydrogen-bond interactions with the ubiquitin Lys48 side chain. GNE-6776 targets cellular USP7, MDM2, and p53 signalling pathways.GNE-6776 selectively inhibits recombinant USP7 relative to 36 other deubiquitinases. GNE-6776 remains selective even at 100?uM, a more than sixfold higher concentration than used in cellular assays. GNE-6776 significantly inhibits USP7 while remaining selective against 44-47 other detected deubiquitinases^[1]. In Vivo: Although efficacious exposure is only transiently achieved, GNE-6776 causes modest, although significant, EOL-1 xenograft growth delay^[1].