1. Metabolic Enzyme/Protease
  2. Proteasome
  3. PD150606

PD 150606 is a selective, cell-permeable non-peptide calpain inhibitor with Ki values of 0.21 μM and 0.37 μM for μ- and m-calpains respectively, which is neuroprotective.

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

CAS No. : 179528-45-1

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10 mM * 1 mL in DMSO
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Customer Review

Based on 14 publication(s) in Google Scholar

Other Forms of PD150606:

Top Publications Citing Use of Products

    PD150606 purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2024 Sep 30;23(1):215.  [Abstract]

    Western blot analysis of RXRα expression after 24 h of treatment with PD150606 (200 nM, m-calpain inhibitor) or ZFY-CHO (10 µM, CTSL inhibitor).

    PD150606 purchased from MedChemExpress. Usage Cited in: Cell Rep. 2023 Dec 2;42(12):113522.  [Abstract]

    Representative immunofluorescence images of DRG neurons seeded on laminin-coated glass slides and treated with culture medium (control), 10 μM PD150606 or 30 μM Yoda1 for 24 hours.

    PD150606 purchased from MedChemExpress. Usage Cited in: Cell Rep. 2023 Dec 2;42(12):113522.  [Abstract]

    Western blots of integrin-β1, SN25, and GAPDH in DRG neurons seeded on glass slides and treated with 10 μM PD150606 for 30 min at DIV1.

    PD150606 purchased from MedChemExpress. Usage Cited in: Cell Rep. 2023 Dec 2;42(12):113522.  [Abstract]

    Representative images were cultured on substrates at 5.0 and 20 kPa and incubated for 24 hours with medium (control) or 10 μM PD150606.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    PD 150606 is a selective, cell-permeable non-peptide calpain inhibitor with Ki values of 0.21 μM and 0.37 μM for μ- and m-calpains respectively, which is neuroprotective[1].

    IC50 & Target

    Ki: 0.21 μM (μ-calpains), 0.37 μM (m-calpains)[1]

    In Vitro

    PD150606 interacts with both calcium-binding domains (μ- and m-calpains) of Calpain[1].
    PD150606 attenuates hypoxic/hypoglycemic injury to cerebrocortical neurons in culture and excitotoxic injury to Purkinje cells in cerebellar slices[1].
    PD 150606 (25 μM; 0-12 hours) reduces Cycloheximide (10 mg/ml) -triggered apoptosis of neutrophils[2].

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

    Molecular Weight

    306.12

    Formula

    C9H7IO2S

    CAS No.
    Appearance

    Solid

    Color

    Off-white to yellow

    SMILES

    O=C(O)/C(S)=C/C1=CC=C(I)C=C1

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    4°C, protect from light

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    Solvent & Solubility
    In Vitro: 

    DMSO : ≥ 28 mg/mL (91.47 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 3.2667 mL 16.3335 mL 32.6669 mL
    5 mM 0.6533 mL 3.2667 mL 6.5334 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 (protect from light). 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)

    Mass
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    Volume
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    Molecular Weight *

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

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    Volume (start)

    V1

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    Volume (final)

    V2

    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: ≥ 2.5 mg/mL (8.17 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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: 2.5 mg/mL (8.17 mM); Suspended solution; Need ultrasonic

      This protocol yields a suspended solution of 2.5 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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:

    Dosage

    mg/kg

    Animal weight
    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Please enter your animal formula composition:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    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).

    *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

    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: 98.61%

    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 (protect from light). 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 3.2667 mL 16.3335 mL 32.6669 mL 81.6673 mL
    5 mM 0.6533 mL 3.2667 mL 6.5334 mL 16.3335 mL
    10 mM 0.3267 mL 1.6333 mL 3.2667 mL 8.1667 mL
    15 mM 0.2178 mL 1.0889 mL 2.1778 mL 5.4445 mL
    20 mM 0.1633 mL 0.8167 mL 1.6333 mL 4.0834 mL
    25 mM 0.1307 mL 0.6533 mL 1.3067 mL 3.2667 mL
    30 mM 0.1089 mL 0.5444 mL 1.0889 mL 2.7222 mL
    40 mM 0.0817 mL 0.4083 mL 0.8167 mL 2.0417 mL
    50 mM 0.0653 mL 0.3267 mL 0.6533 mL 1.6333 mL
    60 mM 0.0544 mL 0.2722 mL 0.5444 mL 1.3611 mL
    80 mM 0.0408 mL 0.2042 mL 0.4083 mL 1.0208 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:
    PD150606
    Cat. No.:
    HY-100529
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