PVD-06 is a selective PROTAC PTPN2 degrader with a DC 50 of 217 nM (selectivity index >60-fold over PTP1B). PVD-06 induces PTPN2 degradation via a VHL-, ubiquitin, and proteasome-dependent pathway. PVD-06 can promote T cell activation and amplify IFN-γ -mediated anticancer activity. PVD-06 can be used to further investigate PTPN2 in diseases such as leukemia and melanoma. (Pink: PTPN2 ligand ( HY-168691 ); Blue: VHL ligand ( HY-112078 ); Black: linker ( HY-B0236 )).
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