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  3. (20S)-Protopanaxadiol

(20S)-Protopanaxadiol  (Synonyms: 20-Epiprotopanaxadiol; 20(S)-APPD)

製品番号: HY-N0797 純度: 99.94%
COA 取扱説明書 Technical Support

20S-protopanaxadiol (aPPD) is a metabolite of ginseng saponins, inhibits Akt activity and induces apoptosis in various tumor cells.

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CAS 番号 : 30636-90-9

容量 価格(税別) 在庫状況 数量
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
USD 56 在庫あり
Solution
10 mM * 1 mL in DMSO USD 56 在庫あり
Solid
5 mg $55 在庫あり
10 mg $88 在庫あり
50 mg $294 在庫あり
100 mg   お問い合わせ  
200 mg   お問い合わせ  

* アイテムを追加する前、数量をご選択ください

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カスタマーレビュー

Based on 3 publication(s) in Google Scholar

Other Forms of (20S)-Protopanaxadiol:

Top Publications Citing Use of Products

    (20S)-Protopanaxadiol purchased from MedChemExpress. Usage Cited in: Ren Fail. 2025 Dec;47(1):2526688.  [Abstract]

    Representative immunohistochemical staining of TGF-β1 in kidney sections treated with (20S)-Protopanaxadiol (PPD) (20 mg/kg, i.g.).

    (20S)-Protopanaxadiol purchased from MedChemExpress. Usage Cited in: Ren Fail. 2025 Dec;47(1):2526688.  [Abstract]

    Western blot analysis of TGF-β1, α-smooth muscle actin (α-SMA), Smad3, phosphorylated Smad3 (p-Smad3), and Smad4 expression in DN mice after (20S)-Protopanaxadiol (PPD) (20 mg/kg) intragastric administration.

    (20S)-Protopanaxadiol purchased from MedChemExpress. Usage Cited in: Ren Fail. 2025 Dec;47(1):2526688.  [Abstract]

    Body weight following 3-week (20S)-Protopanaxadiol (PPD) (20 mg/kg, i.g.). administration.

    (20S)-Protopanaxadiol purchased from MedChemExpress. Usage Cited in: Ren Fail. 2025 Dec;47(1):2526688.  [Abstract]

    Serum Creatinine levels of mice in each group after (20S)-Protopanaxadiol (PPD) (20 mg/kg) intragastric administration.
    • 生物活性

    • 純度とドキュメンテーション

    • 参考文献

    • カスタマーレビュー

    製品説明

    20S-protopanaxadiol (aPPD) is a metabolite of ginseng saponins, inhibits Akt activity and induces apoptosis in various tumor cells[1].

    Cellular Effect
    Cell Line Type Value Description References
    A549 IC50
    99.89 μM
    Compound: PPD
    Cytotoxicity against human A549 cells after 72 hrs by MTT assay
    Cytotoxicity against human A549 cells after 72 hrs by MTT assay
    [PMID: 21216145]
    A549 IC50
    99.89 μM
    Compound: PPD
    Cytotoxicity against human A549 cells after 72 hrs by MTT assay
    Cytotoxicity against human A549 cells after 72 hrs by MTT assay
    [PMID: 22342101]
    BMMC IC50
    11.8 μM
    Compound: PPD
    Anti-osteoclastogenic activity in C57/BL6 mouse BMMC cells assessed as inhibition of RANKL-induced osteoclast differentiation incubated for 5 to 7 days in presence of M-CSF by TRAP staining based microscopic analysis relative to control
    Anti-osteoclastogenic activity in C57/BL6 mouse BMMC cells assessed as inhibition of RANKL-induced osteoclast differentiation incubated for 5 to 7 days in presence of M-CSF by TRAP staining based microscopic analysis relative to control
    [PMID: 37597216]
    COLO 205 IC50
    49.16 μM
    Compound: PPD
    Cytotoxicity against human COLO205 cells after 72 hrs by MTT assay
    Cytotoxicity against human COLO205 cells after 72 hrs by MTT assay
    [PMID: 21216145]
    DU-145 IC50
    60.41 μM
    Compound: PPD
    Cytotoxicity against human DU145 cells after 72 hrs by MTT assay
    Cytotoxicity against human DU145 cells after 72 hrs by MTT assay
    [PMID: 21216145]
    Hep 3B2 IC50
    14.69 μM
    Compound: PPD
    Cytotoxicity against human Hep3B cells after 72 hrs by MTT assay
    Cytotoxicity against human Hep3B cells after 72 hrs by MTT assay
    [PMID: 22342101]
    HepG2 IC50
    39.42 μM
    Compound: PPD
    Cytotoxicity against human HepG2 cells after 72 hrs by MTT assay
    Cytotoxicity against human HepG2 cells after 72 hrs by MTT assay
    [PMID: 21216145]
    HepG2 IC50
    45.67 μM
    Compound: 3
    Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
    Cytotoxicity against human HepG2 cells after 48 hrs by MTT assay
    [PMID: 26420067]
    HL-60 IC50
    15.53 μM
    Compound: 3
    Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
    Cytotoxicity against human HL60 cells after 48 hrs by MTT assay
    [PMID: 26420067]
    HL-60 IC50
    27.06 μM
    Compound: PPD
    Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
    Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
    [PMID: 21216145]
    HUVEC EC50
    2.16 μg/mL
    Compound: 1
    Antiproliferative activity against HUVEC cells after 72 hrs
    Antiproliferative activity against HUVEC cells after 72 hrs
    [PMID: 18271556]
    LLC-PK1 IC50
    36.7 μM
    Compound: PPD
    Cytotoxicity against pig LLC-PK1 cells after 4 hrs by MTT assay
    Cytotoxicity against pig LLC-PK1 cells after 4 hrs by MTT assay
    [PMID: 25453798]
    MCF7 IC50
    6.62 μM
    Compound: PPD
    Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
    Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
    [PMID: 21216145]
    MDA-MB-231 IC50
    5.9 μM
    Compound: PPD
    Antiproliferative activity against human MDA-MB-231 cells after 4 hrs by MTT assay
    Antiproliferative activity against human MDA-MB-231 cells after 4 hrs by MTT assay
    [PMID: 25453798]
    SF-188 IC50
    24 μM
    Compound: 1
    Cytotoxicity against human SF188 cells after 24 hrs
    Cytotoxicity against human SF188 cells after 24 hrs
    [PMID: 17261067]
    U-87MG ATCC IC50
    36.74 μM
    Compound: PPD
    Cytotoxicity against human U87 cells after 72 hrs by MTT assay
    Cytotoxicity against human U87 cells after 72 hrs by MTT assay
    [PMID: 22342101]
    U-87MG ATCC IC50
    38 μM
    Compound: 1
    Cytotoxicity against human U87MG cells after 24 hrs
    Cytotoxicity against human U87MG cells after 24 hrs
    [PMID: 17261067]
    体外実験

    20S-protopanaxadiol treatment upregulates the flotillin-1 level in the rafts of N2a cells to 142.91±10.71% of the control. 20S-protopanaxadiol can have an opposite effect on raft resident protein flotillin-1, depending on the cell type[1].

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

    分子量

    460.73

    分子式

    C30H52O3

    CAS 番号
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    C[C@]([C@@](C[C@H]1O)([H])[C@]2(CC[C@@H]3O)C)(CC[C@@]2([H])C3(C)C)[C@]4([C@@]1([H])[C@]([C@@](C)(O)CC/C=C(C)/C)([H])CC4)C

    Structure Classification
    Initial Source
    輸送条件

    Room temperature in continental US; may vary elsewhere.

    保管条件
    Powder -20°C 3 years
      4°C 2 years
    In solvent -80°C 6 months
      -20°C 1 month
    溶剤 & 溶解度
    体外: 

    DMSO : 50 mg/mL (108.52 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 2.1705 mL 10.8523 mL 21.7047 mL
    5 mM 0.4341 mL 2.1705 mL 4.3409 mL
    10 mM 0.2170 mL 1.0852 mL 2.1705 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    • 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)

    一般には略語で表示されます:C1V1 = C2V2

    濃度 (開始)

    C1

    ×
    体積 (開始)

    V1

    =
    濃度 (終了)

    C2

    ×
    体積 (終了)

    V2

    体内:

    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    90% Corn Oil

      Solubility: ≥ 2.5 mg/mL (5.43 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).
    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.
    純度とドキュメンテーション

    純度: 99.94%

    参考文献

    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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 2.1705 mL 10.8523 mL 21.7047 mL 54.2617 mL
    5 mM 0.4341 mL 2.1705 mL 4.3409 mL 10.8523 mL
    10 mM 0.2170 mL 1.0852 mL 2.1705 mL 5.4262 mL
    15 mM 0.1447 mL 0.7235 mL 1.4470 mL 3.6174 mL
    20 mM 0.1085 mL 0.5426 mL 1.0852 mL 2.7131 mL
    25 mM 0.0868 mL 0.4341 mL 0.8682 mL 2.1705 mL
    30 mM 0.0723 mL 0.3617 mL 0.7235 mL 1.8087 mL
    40 mM 0.0543 mL 0.2713 mL 0.5426 mL 1.3565 mL
    50 mM 0.0434 mL 0.2170 mL 0.4341 mL 1.0852 mL
    60 mM 0.0362 mL 0.1809 mL 0.3617 mL 0.9044 mL
    80 mM 0.0271 mL 0.1357 mL 0.2713 mL 0.6783 mL
    100 mM 0.0217 mL 0.1085 mL 0.2170 mL 0.5426 mL
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    • Molarity Calculator

    • Dilution Calculator

    The molarity calculator equation

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    質量   濃度   体積   分子量 *
    = × ×

    The dilution calculator equation

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

    一般には略語で表示されます:C1V1 = C2V2

    濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
    × = ×
    C1   V1   C2   V2
    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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    Inquiry Information

    製品名:
    (20S)-Protopanaxadiol
    製品番号:
    HY-N0797
    数量:
    MCE 日本正規代理店: