1. Metabolic Enzyme/Protease Autophagy
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  3. (-)-Epigallocatechin

(-)-Epigallocatechin  (Synonyms: Epigallocatechin; L-Epigallocatechin)

Cat. No.: HY-N0225 Pureza: 99.66%
Instrucciones de manejo Technical Support

(-)-Epigallocatechin (Epigallocatechin) is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils.

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No. CAS : 970-74-1

Tamaño Precio Stock Cantidad
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
En stock
Solution
10 mM * 1 mL in DMSO En stock
Solid
5 mg En stock
10 mg En stock
25 mg En stock
50 mg En stock
100 mg En stock
250 mg En stock
500 mg En stock
1 g   Obtener un presupuesto  
5 g   Obtener un presupuesto  

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Revisión del cliente

Based on 5 publication(s) in Google Scholar

Other Forms of (-)-Epigallocatechin:

Top Publications Citing Use of Products

    (-)-Epigallocatechin purchased from MedChemExpress. Usage Cited in: Pathogens. 2026 Mar 20;15(3):334.  [Abstract]

    Immunofluorescence analysis presenting that EGC ((-)-Epigallocatechin) (5-20 μM) exerts a slight inhibitory effect on the expression of ZIKV capsid protein (red) in A549 cells. Nuclei were counterstained in blue with DAPI. Original magnification was 200×, and the scale bar represented 50 μm. The infection rate was quantified as the ratio of ZIKV-positive cells to the total number of DAPI-positive cells.

    (-)-Epigallocatechin purchased from MedChemExpress. Usage Cited in: Pathogens. 2026 Mar 20;15(3):334.  [Abstract]

    (-)-Epigallocatechin (EGC) (40 μM; 10-60 days). The hemolysis rate test showed that GTE mildly decreases the hemolysis rate of RBCs during storage.
    • Actividad biológica

    • Pureza y Documentación

    • Referencias

    • Revisión del cliente

    Descripciòn

    (-)-Epigallocatechin (Epigallocatechin) is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils.

    Cellular Effect
    Cell Line Type Value Description References
    BV-2 IC50
    >100 μM
    Compound: 14
    Antineuroinflammatory activity in human BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction
    Antineuroinflammatory activity in human BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction
    [PMID: 27623545]
    H9 IC50
    1.8 μg/mL
    Compound: 7
    Inhibition of uninfected H9 lymphocytic cell growth
    Inhibition of uninfected H9 lymphocytic cell growth
    10.1016/0960-894X(96)00095-9
    HUVEC IC50
    8 μM
    Compound: 42
    Inhibition of NADPH oxidase in Homo sapiens (human) HUVEC cells
    Inhibition of NADPH oxidase in Homo sapiens (human) HUVEC cells
    10.1007/s00044-012-0353-y
    MT4 CC50
    16.1 μg/mL
    Compound: 13
    Cytotoxicity against human MT4 cells by MTT assay
    Cytotoxicity against human MT4 cells by MTT assay
    [PMID: 10425115]
    MT4 IC50
    >16.1 μg/mL
    Compound: 13
    Antiviral activity against HIV infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
    Antiviral activity against HIV infected in human MT4 cells assessed as inhibition of virus-induced cytopathic effect by MTT assay
    [PMID: 10425115]
    In Vitro

    (-)-Epigallocatechin (EGC) is a potent inhibitor of amyloidogenic cystatin I66Q amyloid fibril formation in vitro. Computational analysis suggests that (-)-Epigallocatechin prevents amyloidogenic cystatin fibril formation by stabilizing the molecule in its native-like state as opposed to redirecting aggregation to disordered, amorphous aggregates [1]. Combined curcumin and EGCG treatment reduced the cancer stem-like Cluster of differentiation 44 (CD44)-positive cell population. Western blot and immunoprecipitation analyses revealed that curcumin and (-)-Epigallocatechin (EGC) specifically inhibited STAT3 phosphorylation and STAT3-NFkB interaction was retained [2]. (-)-Epigallocatechin (EGC) exhibits a MIC and MBC of 5 μg/mL and 20 μg/mL respectively and effectively eradicated E. faecalis biofilms. (-)-Epigallocatechin induces the formation of hydroxyl radicals in E. faecalis. The addition of DIP protected E. faecalis against EGCG-mediated antibacterial effects. At sub-MIC, (-)-Epigallocatechin induces significant down-regulation of E. faecalis virulence genes [3].

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

    Peso molecular

    306.27

    Fòrmula

    C15H14O7

    No. CAS
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O[C@H]1[C@@H](C2=CC(O)=C(O)C(O)=C2)OC3=CC(O)=CC(O)=C3C1

    Structure Classification
    Initial Source
    Envío

    Room temperature in continental US; may vary elsewhere.

    Almacenamiento
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 6 months
    -20°C 1 month
    Solvente y solubilidad
    In Vitro: 

    DMSO : 66.67 mg/mL (217.68 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 3.2651 mL 16.3255 mL 32.6509 mL
    5 mM 0.6530 mL 3.2651 mL 6.5302 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.

    • Calculadora de molaridad

    • Calculadora de dilución

    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% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (8.16 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 (8.16 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:

    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).
    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.
    Pureza y Documentación

    Purity: 99.66%

    Referencias

    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 3.2651 mL 16.3255 mL 32.6509 mL 81.6273 mL
    5 mM 0.6530 mL 3.2651 mL 6.5302 mL 16.3255 mL
    10 mM 0.3265 mL 1.6325 mL 3.2651 mL 8.1627 mL
    15 mM 0.2177 mL 1.0884 mL 2.1767 mL 5.4418 mL
    20 mM 0.1633 mL 0.8163 mL 1.6325 mL 4.0814 mL
    25 mM 0.1306 mL 0.6530 mL 1.3060 mL 3.2651 mL
    30 mM 0.1088 mL 0.5442 mL 1.0884 mL 2.7209 mL
    40 mM 0.0816 mL 0.4081 mL 0.8163 mL 2.0407 mL
    50 mM 0.0653 mL 0.3265 mL 0.6530 mL 1.6325 mL
    60 mM 0.0544 mL 0.2721 mL 0.5442 mL 1.3605 mL
    80 mM 0.0408 mL 0.2041 mL 0.4081 mL 1.0203 mL
    100 mM 0.0327 mL 0.1633 mL 0.3265 mL 0.8163 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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    Nombre del producto:
    (-)-Epigallocatechin
    Cat. No.:
    HY-N0225
    Cantidad:
    MCE Japan Authorized Agent: