1. MAPK/ERK Pathway Immunology/Inflammation
  2. MAP4K Interleukin Related
  3. HPK1-IN-68

HPK1-IN-68 (Compound 39) is a HPK1 inhibitor with an IC50 of 2.8 nM. HPK1-IN-68 blocks HPK1 signaling, inhibits HPK1-mediated phosphorylation of SLP76, and promotes the production of the IL-2 cytokine. HPK1-IN-68 antagonizes the immunosuppressive effect mediated by PGE2. HPK1-IN-68 enhances the infiltration of CD3+/CD8+ T cells into tumor tissues. HPK1-IN-68 exerts T cell-dependent antitumor efficacy in a mouse colon cancer model. HPK1-IN-68 exhibits significant synergistic antitumor effects when used in combination with anti-PD-1. HPK1-IN-68 is applicable to research related to colon cancer.

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HPK1-IN-68

HPK1-IN-68 Chemical Structure

CAS No. : 3078477-58-1

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Description

HPK1-IN-68 (Compound 39) is a HPK1 inhibitor with an IC50 of 2.8 nM. HPK1-IN-68 blocks HPK1 signaling, inhibits HPK1-mediated phosphorylation of SLP76, and promotes the production of the IL-2 cytokine. HPK1-IN-68 antagonizes the immunosuppressive effect mediated by PGE2. HPK1-IN-68 enhances the infiltration of CD3+/CD8+ T cells into tumor tissues. HPK1-IN-68 exerts T cell-dependent antitumor efficacy in a mouse colon cancer model. HPK1-IN-68 exhibits significant synergistic antitumor effects when used in combination with anti-PD-1. HPK1-IN-68 is applicable to research related to colon cancer[1].

IC50 & Target[1]

HPK1

2.8 nM (IC50)

IL-2

 

In Vitro

HPK1-IN-68 (pre-equilibrated for 10 min, 1 h) potently inhibits the kinase activity of recombinant HPK1, with an IC50 of 2.8 nM[1].
HPK1-IN-68 (0-1000 nM; 2 h) inhibits HPK1-mediated phosphorylation of SLP76 in Jurkat T cells, with an IC50 of 30.4 nM[1].
HPK1-IN-68 (0.01 nM-1 μM; 48 h) enhances IL-2 cytokine production in CD3/CD28-stimulated Jurkat T cells at submicromolar concentrations[1].
HPK1-IN-68 exhibits moderate metabolic stability in liver microsomes, with a half-life of 26.1 min[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

ELISA Assay[1]

Cell Line: Jurkat T cells
Concentration: 0.01 nM-1 μM
Incubation Time: 48 h
Result: Increased IL-2 production relative to vehicle control at concentrations from 0.01 nM to 100 nM.
Reduced IL-2 production at the highest tested concentration (1 μM).
Parmacokinetics
Species Dose Route T1/2 Vdss AUC0-t AUC0-∞ CL MRT0-∞ Tmax Cmax CL/F Vz/F Bioavailability
Mice[1] 1 mg/kg i.v. 4.8 ± 1.1 h 16.8 ± 4.0 L/kg 260.5 ± 20.9 ng·h/mL 271.3 ± 21.9 ng·h/mL 61.7 ± 5.1 mL/h/kg 4.6 ± 1.1 h / / / / /
Mice[1] 10 mg/kg p.o. 4.2 ± 0.6 h / 743.4 ± 224.1 ng·h/mL 755.8 ± 223.7 ng·h/mL / 4.5 ± 0.2 h 1.7 ± 0.6 h 140.1 ± 42.3 ng/mL 235.7 ± 77.9 mL/min/kg 89.3 ± 42.5 L/kg 28.5 ± 8.6 %
In Vivo

HPK1-IN-68 (10 mg/kg; i.p.; twice daily; 17 days) exerts anti-tumor effects both as a single agent and in combination with anti-PD-1 antibody in a mouse CT26 colon cancer model[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Balb/c (female, 4-5 weeks old, 18-22 g, subcutaneously injected with 5×105 CT26 tumor cells)[1]
Dosage: 10 mg/kg (monotherapy; combination with anti-PD-1)
Administration: i.p.; bid; 17 days (monotherapy); i.p.; bid (combination with anti-PD-1, anti-PD-1 administered on days 0, 3, 7, and 10 at 5 mg/kg i.p.)
Result: Achieved 48% tumor growth inhibition (TGI) as monotherapy.
Achieved 59% TGI with combination index (CI) < 1 and synergy score (SS) > 0 when combined with anti-PD-1 antibody, confirming synergistic activity.
Was well-tolerated, with no significant body weight loss observed.
Increased infiltration of CD3+/CD8+ T cells into tumor tissues, and this effect was amplified when combined with anti-PD-1 antibody.
Molecular Weight

453.51

Formula

C23H28FN7O2

CAS No.
SMILES

NC1=NC=C(C2=CC(C)=C(OCCCN3CC[C@@H](F)C3)C(C)=C2)N=C1N4C=C(C(N)=O)C=N4

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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HPK1-IN-68
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HY-181924
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