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PROTAC HPK1 Degrader-5

PROTAC HPK1 Degrader-5 is a potent and orally active HPK1 PROTAC degrader (DC50 = 5.0 nM; Dmax ≥ 99%) . PROTAC HPK1 Degrader-5 significantly inhibits SLP76 phosphorylation and enhanced ERK pathway activation through degrading HPK1, thereby stimulating IL-2 and IFN-γ release. PROTAC HPK1 Degrader-5 exhibits the ability to overcome the immunosuppressive effects imposed by PGE2, NECA or TGF-β. PROTAC HPK1 Degrader-5 alone efficaciously inhibits tumor growth in an MC38 syngeneic mouse model. PROTAC HPK1 Degrader-5 can be used for the study of tumor (such as colorectal cancer) immunotherapy (Pink: Target protein ligand (HY-175549) ; Blue: E3 ligand (HY-W023573) ; Black: Linker; E3 ligand + Linker (HY-175551) ) [1].

Product Specifications

UNSPSC

12352005

Target

ERK; IFNAR; Interleukin Related; MAP4K; PROTACs

Related Pathways

Immunology/Inflammation; MAPK/ERK Pathway; PROTAC; Stem Cell/Wnt

Field of Research

Cancer; Inflammation/Immunology

Smiles

O=C(N)C1=NC(C2=C(C3=CC=C2)N=CN3C)=C(N=C1NC4=CC=C(C=C4)C5CCN(CC5)C[C@@H]6CCN(C6)C7=CC8=C(C=C7)C(N(C8=O)C9CCC(NC9=O)=O)=O)NC

Molecular Formula

C43H45N11O5

Molecular Weight

795.89

References & Citations

[1]Tong J, et al. Discovery of a Novel Potent and Orally Efficacious PROTAC Degrader of HPK1 for Tumor Immunotherapy. J Med Chem. 2025 Aug 14;68 (15) :15991-16017.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

Cereblon; ERK; IL-2

Curated Selection

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