DD205-291 is a selective, orally active HPK1 PROTAC degrader with a DC 50 of 8.8 nM. By inducing complete degradation of HPK1 protein, DD205-291 simultaneously blocks both its kinase-dependent functions and non-kinase scaffold functions. DD205-291 inhibits the phosphorylation of SLP-76 with an EC 50 of 22.98 nM. DD205-291 induces the production of IL-2 and IFN-γ with EC 50 values of 34.68 nM and 32.6 nM, respectively. Combined with anti- PD1 in mouse models, DD205-291 exerts tumor-suppressive effects with favorable safety profiles. DD205-291 can be used in colon cancer-related research. (Pink: HPK1 ligand ( HY-168283 ); Blue: Cereblon ligand ( HY-W115490 ); Black: linker).
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