1. Protein Tyrosine Kinase/RTK
  2. Itk
  3. Soquelitinib

Soquelitinib (CPI-818) is an orally active and highly selective covalent interleukin-2-inducible kinase (ITK) inhibitor. Soquelitinib is active in six different models of T cell-mediated inflammatory and immune disease, including acute and chronic asthma, pulmonary fibrosis, systemic sclerosis (scleroderma), psoriasis, and acute graft versus host disease with Th2 cytokine product inhibition. Soquelitinib increases tumor infiltration of normal CD8+ cells that possess enhanced T effector function.

For research use only. We do not sell to patients.

CAS No. : 2226636-04-8

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
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Customer Review

Based on 3 publication(s) in Google Scholar

Top Publications Citing Use of Products

    Soquelitinib purchased from MedChemExpress. Usage Cited in: Cell Signal. 2026 Feb:138:112204.  [Abstract]

    Western blot analysis of PLCγ1Y783, LckY394, and Erk1T202Y204/Erksup>2T185Y187, respectively, in samples treated with PP1, Soquelitinib (2 μM), or U0126. One sample is shown here for display.

    Soquelitinib purchased from MedChemExpress. Usage Cited in: Cell Signal. 2026 Feb:138:112204.  [Abstract]

    Western blot analysis of PLCγ1Y783, LckY394, and Erk1T202Y204/Erksup>2T185Y187 phosphorylation in the basal and stimulated states of untreated or kinase inhibitor treated Jurkat T cells with Soquelitinib (2 μM; 0-5 min).
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    Soquelitinib (CPI-818) is an orally active and highly selective covalent interleukin-2-inducible kinase (ITK) inhibitor. Soquelitinib is active in six different models of T cell-mediated inflammatory and immune disease, including acute and chronic asthma, pulmonary fibrosis, systemic sclerosis (scleroderma), psoriasis, and acute graft versus host disease with Th2 cytokine product inhibition. Soquelitinib increases tumor infiltration of normal CD8+ cells that possess enhanced T effector function[1][2][3].

    In Vitro

    Soquelitinib (10 μM, 2 h) inhibits TCR signaling downstream of ITK and blocks lL-2 production in Jurkat cells[1].
    Soquelitinib (10 μM, 1 h) suppresses Th2 associated cytokines and induces Th1 skewing in CD4 T cells[1].

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

    In Vivo

    Soquelitinib (30 mg/kg, oral gavage, twice daily for 20 days) enhances CD8T cell infiltration, increases cytolytic capacity of tumor-infiltrating lymphocytes (TILs) and enhances anti-PD1 and anti-CTLA4 efficacy in the CT26 tumor model[1].

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

    Animal Model: Murine syngeneictumor models[2]
    Dosage: 30 mg/kg
    Administration: oral gavage, twice daily for 20 days
    Result: Induced significantly higher frequency of intra-tumoral CD8 T cells in the CT26 model and a moderate increase in intra-tumoral CD8 infiltration.
    Augmented the antitumor efficacy of immune checkpoint blockade, leading to durable antitumor response in the CT26 model.
    Clinical Trial
    Molecular Weight

    514.66

    Formula

    C25H30N4O4S2

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C(N1C[C@H](N(CCC1)C(C=C)=O)C)C2=C(C=C(C(SC3=CN=C(NC(C4CC4)=O)S3)=C2)C)OC

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 6 months
    -20°C 1 month
    Solvent & Solubility
    In Vitro: 

    DMSO : ≥ 100 mg/mL (194.30 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    *"≥" means soluble, but saturation unknown.

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.9430 mL 9.7152 mL 19.4303 mL
    5 mM 0.3886 mL 1.9430 mL 3.8861 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    • Molarity Calculator

    • Dilution Calculator

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

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    In Vivo:

    Select the appropriate dissolution method based on your experimental animal and administration route.

    For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
    To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 10 mg/mL (19.43 mM); Clear solution

      This protocol yields a clear solution of ≥ 10 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (100.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

      Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 10 mg/mL (19.43 mM); Clear solution

      This protocol yields a clear solution of ≥ 10 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (100.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

      Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

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    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Please enter your animal formula composition:
    %
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    Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
    The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
    Calculation results:
    Working solution concentration: mg/mL
    Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
    Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
     If the continuous dosing period exceeds half a month, please choose this protocol carefully.
    Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
    Purity & Documentation

    Purity: 99.98%

    References

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 1.9430 mL 9.7152 mL 19.4303 mL 48.5758 mL
    5 mM 0.3886 mL 1.9430 mL 3.8861 mL 9.7152 mL
    10 mM 0.1943 mL 0.9715 mL 1.9430 mL 4.8576 mL
    15 mM 0.1295 mL 0.6477 mL 1.2954 mL 3.2384 mL
    20 mM 0.0972 mL 0.4858 mL 0.9715 mL 2.4288 mL
    25 mM 0.0777 mL 0.3886 mL 0.7772 mL 1.9430 mL
    30 mM 0.0648 mL 0.3238 mL 0.6477 mL 1.6192 mL
    40 mM 0.0486 mL 0.2429 mL 0.4858 mL 1.2144 mL
    50 mM 0.0389 mL 0.1943 mL 0.3886 mL 0.9715 mL
    60 mM 0.0324 mL 0.1619 mL 0.3238 mL 0.8096 mL
    80 mM 0.0243 mL 0.1214 mL 0.2429 mL 0.6072 mL
    100 mM 0.0194 mL 0.0972 mL 0.1943 mL 0.4858 mL
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    Help & FAQs
    • 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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    Product Name:
    Soquelitinib
    Cat. No.:
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