1. MAPK/ERK Pathway Stem Cell/Wnt Metabolic Enzyme/Protease
  2. p38 MAPK MEK ERK Endogenous Metabolite
  3. C16-PAF

C16-PAF (PAF (C16)), a phospholipid mediator, is a platelet-activating factor and ligand for PAF G-protein-coupled receptor (PAFR). C16-PAF exhibits anti-apoptotic effect and inhibits caspase-dependent death by activating the PAFR. C16-PAF is a potent MAPK and MEK/ERK activator. C16-PAF induces increased vascular permeability.

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

CAS No. : 74389-68-7

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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 40 publication(s) in Google Scholar

Other Forms of C16-PAF:

Top Publications Citing Use of Products

40 Publications Citing Use of MCE C16-PAF

WB
Cell Proliferation/Viability Assay
IF

    C16-PAF purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 17;16(1):1715.  [Abstract]

    WB was performed to measure the protein levels of pERK1/2 and ERK1/2. C16-PAF (100 nM) facilitates the activation of the MAPK pathway and increases EV-D68 78 replication in CXCL8-silenced cells.

    C16-PAF purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 17;16(1):1715.  [Abstract]

    C16-PAF (100 nM) facilitates the activation of the MAPK pathway and increases EV-D68 replication in CXCL8-silenced cells.

    C16-PAF purchased from MedChemExpress. Usage Cited in: Phytomedicine. 2025 Aug:144:156949.  [Abstract]

    Western blot analysis of p-ERK1/2, p-MEK, HK2, PKM2, and LDHA levels in 143B and U2R cells treated with C16-PAF (1 µM).

    C16-PAF purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2025 Aug 1:235:231-247.  [Abstract]

    In SUM159 cells treated with ERK agonist (1 μM C16-PAF) in combination with indicated concentrations of RES for 12 h, the protein levels of p-ERK1/2, ERK1/2, p-NEDD4L, NEDD4L, p-SGK1, SGK1 and GPX4 were measured by western blotting assays.

    C16-PAF purchased from MedChemExpress. Usage Cited in: J Transl Med. 2023 Aug 7;21(1):532.  [Abstract]

    LN229 and U251 cells were treated with 1.25 µM Mito-LND and/or 20 µM C16-PAF for 36 h, then cell viabilities were evaluated by CCK-8 assay.

    C16-PAF purchased from MedChemExpress. Usage Cited in: J Transl Med. 2023 Aug 7;21(1):532.  [Abstract]

    The effects of Mito-LND and/or C16-PAF (20 µM) treatment on the levels of p-ERK1/2, p-p90RSK, Bcl-2 and Bax in LN229 and U251 cells were assessed by western blot analysis.

    C16-PAF purchased from MedChemExpress. Usage Cited in: J Transl Med. 2023 Aug 7;21(1):532.  [Abstract]

    The effects of Mito-LND and/or C16-PAF (20 µM) treatment on the mitochondrial membrane potential, Scale bar: 40 μm.

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    • Biological Activity

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    • References

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    Description

    C16-PAF (PAF (C16)), a phospholipid mediator, is a platelet-activating factor and ligand for PAF G-protein-coupled receptor (PAFR). C16-PAF exhibits anti-apoptotic effect and inhibits caspase-dependent death by activating the PAFR. C16-PAF is a potent MAPK and MEK/ERK activator. C16-PAF induces increased vascular permeability[1][2][3][4][5].

    IC50 & Target[1][4][5]

    Human Endogenous Metabolite

     

    ERK

     

    MEK

     

    In Vitro

    C16-PAF (PAF (C16); 0.5-1.5 μM; for 24 hours) elicits significant concentration-dependent neuronal loss in PAFR / but not PAFR+/+ cultures. C16-PAF (1 μM) elicits neuronal death in PAFR / cells infected with EGFP alone[1].
    C16-PAF (1 μM; for 24 hours) activates caspase 7 but not caspase 3 in PAFR / neurons[1].
    C16-PAF is synthesized by two distinct pathways; the remodeling pathway and the de novo synthesis pathway. C16-PAF acts by binding to a unique G-protein-coupled seven transmembrane receptor[2][3].
    C16-PAF (1-25 μg/ml; 6, 12, 24 h) inhibits M. smegmatis and M. bovis BCG growth in a time-dependent manner[3].

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

    Cell Viability Assay[1]

    Cell Line: Cerebellar granule neurons (CGNs) from PAFR−/− and PAFR+/+ mice
    Concentration: 0.5-1.5 μM
    Incubation Time: 24 hours
    Result: Elicited significant concentration-dependent neuronal loss in PAFR−/− but not PAFR+/+ cultures in serum-free media.

    Western Blot Analysis[1]

    Cell Line: CGNs
    Concentration: 1 μM
    Incubation Time: 24 hours
    Result: Activated caspase 7 but not caspase 3 in PAFR−/− neurons.
    Molecular Weight

    523.68

    Formula

    C26H54NO7P

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    CCCCCCCCCCCCCCCCOC[C@@H](OC(C)=O)COP(OCC[N+](C)(C)C)([O-])=O

    Structure Classification
    Initial Source
    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    -20°C, stored under nitrogen

    *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

    Solvent & Solubility
    In Vitro: 

    DMSO : 100 mg/mL (190.96 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.9096 mL 9.5478 mL 19.0956 mL
    5 mM 0.3819 mL 1.9096 mL 3.8191 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 (stored under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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    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: ≥ 2.5 mg/mL (4.77 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 (4.77 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 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).

    *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

    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: 99.86%

    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 (stored under nitrogen). 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 1.9096 mL 9.5478 mL 19.0956 mL 47.7391 mL
    5 mM 0.3819 mL 1.9096 mL 3.8191 mL 9.5478 mL
    10 mM 0.1910 mL 0.9548 mL 1.9096 mL 4.7739 mL
    15 mM 0.1273 mL 0.6365 mL 1.2730 mL 3.1826 mL
    20 mM 0.0955 mL 0.4774 mL 0.9548 mL 2.3870 mL
    25 mM 0.0764 mL 0.3819 mL 0.7638 mL 1.9096 mL
    30 mM 0.0637 mL 0.3183 mL 0.6365 mL 1.5913 mL
    40 mM 0.0477 mL 0.2387 mL 0.4774 mL 1.1935 mL
    50 mM 0.0382 mL 0.1910 mL 0.3819 mL 0.9548 mL
    60 mM 0.0318 mL 0.1591 mL 0.3183 mL 0.7957 mL
    80 mM 0.0239 mL 0.1193 mL 0.2387 mL 0.5967 mL
    100 mM 0.0191 mL 0.0955 mL 0.1910 mL 0.4774 mL
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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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    Product Name:
    C16-PAF
    Cat. No.:
    HY-108635
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