1. Metabolic Enzyme/Protease Apoptosis Autophagy
  2. Phosphatase Mitochondrial Metabolism Apoptosis Autophagy
  3. C2 Ceramide

C2 Ceramide (Ceramide 2) is the main lipid of the stratum corneum and a protein phosphatase 1 (PP1) activator. C2 Ceramide activates PP2A and ceramide-activated protein phosphatase (CAPP). C2 Ceramide induces cells differentiation, autophagy and apoptosis, inhibits mitochondrial respiratory chain complex III. C2 Ceramide is also a skin conditioning agent that protects the epidermal barrier from water loss.

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

CAS No. : 3102-57-6

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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 2 publication(s) in Google Scholar

Other Forms of C2 Ceramide:

Top Publications Citing Use of Products

    C2 Ceramide purchased from MedChemExpress. Usage Cited in: Food Funct. 2025 Aug 11;16(16):6422-6433.  [Abstract]

    Western blot analysis for phosphorylation of proteins in NF-κB and MAPK signaling pathways in THP-1 cells treated with BCCY-1 in the presence and absence of C2 ceramide (20 μM, 1-3 h).

    C2 Ceramide purchased from MedChemExpress. Usage Cited in: Food Funct. 2025 Aug 11;16(16):6422-6433.  [Abstract]

    The mRNA expressions of MCP-1 in BCCY-1-treated THP-1 cells incubated with or without C2 ceramide (20 μM) measured by qRT-PCR.
    • Biological Activity

    • Purity & Documentation

    • References

    • Customer Review

    Description

    C2 Ceramide (Ceramide 2) is the main lipid of the stratum corneum and a protein phosphatase 1 (PP1) activator. C2 Ceramide activates PP2A and ceramide-activated protein phosphatase (CAPP). C2 Ceramide induces cells differentiation, autophagy and apoptosis, inhibits mitochondrial respiratory chain complex III. C2 Ceramide is also a skin conditioning agent that protects the epidermal barrier from water loss[1][2][3][4][5].

    IC50 & Target

    Protein phosphatase 1[2]
    PP2A[4]
    Ceramide-activated protein phosphatase (CAPP)[4]
    Apoptosis[1]
    Mitochondrial respiratory chain complex III[1]

    Cellular Effect
    Cell Line Type Value Description References
    CCRF-CEM IC50
    31.6 μM
    Compound: C2-ceramide
    In vitro growth inhibitory effect in human T-cell acute leukemia cells CCRF-CEM
    In vitro growth inhibitory effect in human T-cell acute leukemia cells CCRF-CEM
    [PMID: 11689086]
    FL5.12 IC50
    33 μM
    Compound: 9
    Cytotoxicity against mouse FL5.12A cells after 48 hrs by DAPI staining-based flow cytometric analysis
    Cytotoxicity against mouse FL5.12A cells after 48 hrs by DAPI staining-based flow cytometric analysis
    [PMID: 27475534]
    HCT-116 EC50
    24.5 μM
    Compound: 3, C2-ceramide
    Cytotoxicity against HCT116 cells assessed as cell survival by SRB assay
    Cytotoxicity against HCT116 cells assessed as cell survival by SRB assay
    [PMID: 17561396]
    HL-60 IC50
    26 μM
    Compound: 1a
    Antiproliferative activity against human HL60 cells after 24 hrs by Alamar blue assay
    Antiproliferative activity against human HL60 cells after 24 hrs by Alamar blue assay
    [PMID: 25172146]
    HT-29 IC50
    25.9 μM
    Compound: C2-ceramide
    Antiproliferative activity against human HT-29 cells measured after 72 hrs by sulforhodamine B assay
    Antiproliferative activity against human HT-29 cells measured after 72 hrs by sulforhodamine B assay
    [PMID: 33592537]
    HepG2 IC50
    58 μM
    Compound: 1a
    Antiproliferative activity against human HepG2 cells after 24 hrs by Alamar blue assay
    Antiproliferative activity against human HepG2 cells after 24 hrs by Alamar blue assay
    [PMID: 25172146]
    K562 EC50
    35.1 μM
    Compound: 3, C2-ceramide
    Cytotoxicity against K562 cells assessed as cell survival by MTT assay
    Cytotoxicity against K562 cells assessed as cell survival by MTT assay
    [PMID: 17561396]
    MCF7 IC50
    45.41 μM
    Compound: 1, C2 ceramide
    Cytotoxicity against human MCF7 cells after 24 hrs by CellTiter-Blue assay
    Cytotoxicity against human MCF7 cells after 24 hrs by CellTiter-Blue assay
    [PMID: 19171486]
    MDA-MB-231 IC50
    35.37 μM
    Compound: 1, C2 ceramide
    Cytotoxicity against human MDA-MB-231 cells after 24 hrs by CellTiter-Blue assay
    Cytotoxicity against human MDA-MB-231 cells after 24 hrs by CellTiter-Blue assay
    [PMID: 19171486]
    NCI-H358 EC50
    19.6 μM
    Compound: 3, C2-ceramide
    Cytotoxicity against NCI-H358 cells assessed as cell survival by SRB assay
    Cytotoxicity against NCI-H358 cells assessed as cell survival by SRB assay
    [PMID: 17561396]
    NHDF IC50
    66.5 μM
    Compound: 1, C2 ceramide
    Cytotoxicity against NHDF after 24 hrs by CellTiter-Blue assay
    Cytotoxicity against NHDF after 24 hrs by CellTiter-Blue assay
    [PMID: 19171486]
    PC-12 IC50
    98 μM
    Compound: 1a
    Antiproliferative activity against rat PC12 cells after 24 hrs by Alamar blue assay
    Antiproliferative activity against rat PC12 cells after 24 hrs by Alamar blue assay
    [PMID: 25172146]
    SK-BR-3 IC50
    49.2 μM
    Compound: 1, C2 ceramide
    Cytotoxicity against human SKBR3 cells after 24 hrs by CellTiter-Blue assay
    Cytotoxicity against human SKBR3 cells after 24 hrs by CellTiter-Blue assay
    [PMID: 19171486]
    SUP-T1 IC50
    41.44 μM
    Compound: 1, C2 ceramide
    Cytotoxicity against human SupT1 cells after 24 hrs by CellTiter-Blue assay
    Cytotoxicity against human SupT1 cells after 24 hrs by CellTiter-Blue assay
    [PMID: 19171486]
    SUP-T1 IC50
    > 200 μM
    Compound: 2
    Cytotoxicity against human SupT1 cells after 24 hrs by CellTiter-Blue assay
    Cytotoxicity against human SupT1 cells after 24 hrs by CellTiter-Blue assay
    [PMID: 19171486]
    In Vitro

    C2 Ceramide (5 nM-200 μM; 24 hours; primary mouse osteoblasts) treatment (≤500 nM) promots osteoblast viability, whilst concentrations ≥2 μM significantly reduces osteoblast viability in a dose- and time-dependent manner[1].
    C2 Ceramide increases cytoplasmic histone-associated DNA fragments by 5.7- and 11.2-fold at 50 μM and 100 μM C2 Ceramide concentrations respectively in osteoblasts. At these higher concentrations, C2 Ceramide is a potent inducer of apoptosis in osteoblasts[1].
    C2 Ceramide up-regulates mRNA expression of angiogenic genes in human dental pulp cells (HDPCs) and increases the migration and capillary tube formation of endothelial cells, whereas PP1 small interfering RNA shows opposite effects. Human dental pulp cells (HDPCs) increases levels of bone morphogenetic protein 2, phosphorylation of Smad 1/5/8, and mRNA expression of runt-related transcription factor 2 and osterix[2].

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

    Cell Viability Assay[1]

    Cell Line: Primary mouse osteoblasts
    Concentration: 5 nM-200 µM
    Incubation Time: 24 hours
    Result: Murine osteoblasts demonstrated a dose-dependent increase in their survival rate when exposed to low concentrations of 5-500 n M. Increasing concentrations of 20-200µM caused a dose-dependent decrease in mitochondrial succinate dehydrogenase activity and osteoblast survival.
    In Vivo

    The PP1 activator C2 Ceramide increases alkaline phosphatase activity, mineralizes nodule formation, and mRNA expression of dentin matrix protein 1 and dentin sialophosphoprotein. In contrast, knockdown by PP1 small interfering RNA inhibits odontoblastic differentiation[2].

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

    Molecular Weight

    341.53

    Formula

    C20H39NO3

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O[C@H](/C=C/CCCCCCCCCCCCC)[C@H](CO)NC(C)=O

    Shipping

    Room temperature in continental US; may vary elsewhere.

    Storage

    -20°C, sealed storage, away from moisture

    *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

    Solvent & Solubility
    In Vitro: 

    Ethanol : 100 mg/mL (292.80 mM; Need ultrasonic)

    DMSO : 50 mg/mL (146.40 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 2.9280 mL 14.6400 mL 29.2800 mL
    5 mM 0.5856 mL 2.9280 mL 5.8560 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 (sealed storage, away from moisture). 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
    =
    Concentration
    ×
    Volume
    ×
    Molecular Weight *

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

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

    C1

    ×
    Volume (start)

    V1

    =
    Concentration (final)

    C2

    ×
    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% EtOH    90% Corn Oil

      Solubility: 5 mg/mL (14.64 mM); Clear solution; Need ultrasonic

      This protocol yields a clear solution of 5 mg/mL. If the continuous dosing period exceeds half a month, please choose this protocol carefully.

      Taking 1 mL working solution as an example, add 100 μL EtOH stock solution (50.0 mg/mL) to 900 μL Corn oil, and mix evenly.

    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% Corn Oil

      Solubility: ≥ 2.5 mg/mL (7.32 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

    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 (sealed storage, away from moisture)

    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: 99.85%

    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 (sealed storage, away from moisture). 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 / Ethanol 1 mM 2.9280 mL 14.6400 mL 29.2800 mL 73.2000 mL
    5 mM 0.5856 mL 2.9280 mL 5.8560 mL 14.6400 mL
    10 mM 0.2928 mL 1.4640 mL 2.9280 mL 7.3200 mL
    15 mM 0.1952 mL 0.9760 mL 1.9520 mL 4.8800 mL
    20 mM 0.1464 mL 0.7320 mL 1.4640 mL 3.6600 mL
    25 mM 0.1171 mL 0.5856 mL 1.1712 mL 2.9280 mL
    30 mM 0.0976 mL 0.4880 mL 0.9760 mL 2.4400 mL
    40 mM 0.0732 mL 0.3660 mL 0.7320 mL 1.8300 mL
    50 mM 0.0586 mL 0.2928 mL 0.5856 mL 1.4640 mL
    60 mM 0.0488 mL 0.2440 mL 0.4880 mL 1.2200 mL
    80 mM 0.0366 mL 0.1830 mL 0.3660 mL 0.9150 mL
    100 mM 0.0293 mL 0.1464 mL 0.2928 mL 0.7320 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:
    C2 Ceramide
    Cat. No.:
    HY-101180
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