1. Cell Cycle/DNA Damage
  2. Telomerase
  3. Ceramides Mixture

Ceramides Mixture is an endogenous ceramide and consists of hydroxy and non-hydroxy fatty acid-containing ceramides. Ceramides Mixture is a main lipid component of the permeability barrier in epidermis. Ceramides Mixture is involved in the regulation of growth inhibition, cell cycle arrest, and modulation of telomerase activity.

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CAS No. : 100403-19-8

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    Ceramides Mixture purchased from MedChemExpress. Usage Cited in: ACS Cent Sci. 2025 Jul 29;11(9):1682-1699.

    Representative immunofluorescence images of OLFM4 (green) in intestinal organoids under Ceramides Mixture (Ceramide) (10 μg/mL; 48 h) and ceramide+AS-IV (5 μM; 48 h) treatments.

    Ceramides Mixture purchased from MedChemExpress. Usage Cited in: ACS Cent Sci. 2025 Jul 29;11(9):1682-1699.

    Representative images of intestinal organoids treated with Ceramides Mixture (Ceramide) (10 μg/mL; 48 h) or ceramide with AS-IV (ceramide+AS-IV (5 μM; 48 h)).

    Ceramides Mixture purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2023 Apr 11;15(4):e17450.  [Abstract]

    The relative cell viability of KGN cells with Ceramides Mixture (Cer, 30-60 μM; 48 h) treatment. N = 6.

    Ceramides Mixture purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2023 Apr 11;15(4):e17450.  [Abstract]

    The percentage of Annexin V positive cells of KGN cells with Ceramides Mixture (Cer, 40 μM; 48 h) treatment. N = 3

    Ceramides Mixture purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2023 Apr 11;15(4):e17450.  [Abstract]

    Decreases of E2 secretions from KGN cells treated with Ceramides Mixture (Cer, 30-60 μM; 48 h). N = 3.
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    Description

    Ceramides Mixture is an endogenous ceramide and consists of hydroxy and non-hydroxy fatty acid-containing ceramides. Ceramides Mixture is a main lipid component of the permeability barrier in epidermis. Ceramides Mixture is involved in the regulation of growth inhibition, cell cycle arrest, and modulation of telomerase activity[1][2].

    In Vitro

    Endogenous Ceramides (generated in response to bacterial sphingomyelinase overexpression or daunorubicin treatment) inhibits mRNA synthesis of telomerase reverse transcriptase and telomerase activity via inactivation of c-Myc transcription factor in the A549 human lung adenocarcinoma cell line[1].
    The sustained generation of long chain endogenous ceramide requires the biochemical recycling of the sphingosine backbone of C6-ceramide, which involves deacylation and reacylation of ceramide for the generation of endogenous long chain ceramide (mainly C16:0- and C24:1-Ceramides), most likely by CoA-dependent ceramide synthase, which is inhibited by fumonisin B1. In A549 cells the generation of long chain endogenous ceramide mediates the effects of exogenous C6-ceramide on growth inhibition, cell cycle arrest, and the modulation of telomerase activity[1].

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

    CAS No.
    Appearance

    Solid

    Color

    White to light yellow

    SMILES

    [Ceramides Mixture]

    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 : 1 mg/mL (ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    H2O : < 0.1 mg/mL (insoluble)

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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: ≥ 0.1 mg/mL; Clear solution

      This protocol yields a clear solution of ≥ 0.1 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (1.0 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: ≥ 0.1 mg/mL; Clear solution

      This protocol yields a clear solution of ≥ 0.1 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (1.0 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.
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    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).
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    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: 99.8%

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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:
    Ceramides Mixture
    Cat. No.:
    HY-113679
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