1. Autophagy
  2. Autophagy
  3. Schisandrin

シザンドリン  (Synonyms: Schisandrin; Schizandrin; Schizandrol; Schizandrol-A)

製品番号: HY-N0691 純度: 99.97%
COA 取扱説明書 Technical Support

Schisandrin (Schizandrin), a dibenzocyclooctadiene lignan, is isolated from the fruit of Schisandra chinensis Baill. Schisandrin exhibits antioxidant, hepatoprotective, anti-cancer and anti-inflammatory activities. Schisandrin also can reverses memory impairment in rats.

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CAS 番号 : 7432-28-2

容量 価格(税別) 在庫状況 数量
>無料サンプル (0.1 - 0.2 mg)   今すぐ申し込む  
5 mg $50 在庫あり
10 mg $70 在庫あり
25 mg $125 在庫あり
50 mg $175 在庫あり
100 mg $262 在庫あり
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カスタマーレビュー

Based on 3 publication(s) in Google Scholar

Other Forms of Schisandrin:

Top Publications Citing Use of Products
Cell Proliferation/Viability Assay
RT-PCR
WB
Apoptosis Analysis
Bio/Physico-chemical Assay

    Schisandrin purchased from MedChemExpress. Usage Cited in: J Ovarian Res. 2025 Jan 28;18(1):16.  [Abstract]

    The viability of KGN cells treated with Schisandrin at different concentrations (0, 1.25, 2.5, 5, 10 and 20 µM) for 24 h was detected by CCK-8 method.

    Schisandrin purchased from MedChemExpress. Usage Cited in: J Ovarian Res. 2025 Jan 28;18(1):16.  [Abstract]

    The mRNA expression levels of IL-1β, IL-6 and iNOS in KGN cells were detected by RT-qPCR treated with Schisandrin (20 μM).

    Schisandrin purchased from MedChemExpress. Usage Cited in: J Ovarian Res. 2025 Jan 28;18(1):16.  [Abstract]

    The protein expression levels of Bcl-2 and Bax were detected by Western blot treated with Schisandrin (20 μM).

    Schisandrin purchased from MedChemExpress. Usage Cited in: J Ovarian Res. 2025 Jan 28;18(1):16.  [Abstract]

    Apoptosis was assessed by flow cytometry treated with Schisandrin (20 μM).

    Schisandrin purchased from MedChemExpress. Usage Cited in: J Ovarian Res. 2025 Jan 28;18(1):16.  [Abstract]

    The levels of MDA and SOD were detected by the corresponding detection kit treated with Schisandrin (20 μM).
    • 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

    Schisandrin (Schizandrin), a dibenzocyclooctadiene lignan, is isolated from the fruit of Schisandra chinensis Baill. Schisandrin exhibits antioxidant, hepatoprotective, anti-cancer and anti-inflammatory activities. Schisandrin also can reverses memory impairment in rats[1][2][3].

    Cellular Effect
    Cell Line Type Value Description References
    A549 IC50
    20.7 μM
    Compound: Schizandrin
    Antiproliferative activity against human A549 cells after 72 hrs by SRB assay
    Antiproliferative activity against human A549 cells after 72 hrs by SRB assay
    [PMID: 18063366]
    A549 IC50
    21.65 μM
    Compound: 1
    Antiproliferative activity against human A549 cells after 48 hrs by MTT assay
    Antiproliferative activity against human A549 cells after 48 hrs by MTT assay
    [PMID: 29501940]
    A549 IC50
    8.5 μM
    Compound: 1
    Antiproliferative activity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    Antiproliferative activity against human A549 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    [PMID: 32631552]
    DU-145 IC50
    13.09 μM
    Compound: 1
    Antiproliferative activity against human DU145 cells after 48 hrs by MTT assay
    Antiproliferative activity against human DU145 cells after 48 hrs by MTT assay
    [PMID: 29501940]
    DU-145 IC50
    5.38 μM
    Compound: 1
    Antiproliferative activity against human DU145 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    Antiproliferative activity against human DU145 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    [PMID: 32631552]
    H9 IC50
    > 58 μM
    Compound: schisandrin
    Cytotoxicity against human H9 cells after 4 days
    Cytotoxicity against human H9 cells after 4 days
    [PMID: 17190445]
    HCT-15 IC50
    50.2 μM
    Compound: Schizandrin
    Antiproliferative activity against human HCT15 cells after 72 hrs by SRB assay
    Antiproliferative activity against human HCT15 cells after 72 hrs by SRB assay
    [PMID: 18063366]
    HEK293 IC50
    80.47 μM
    Compound: 1
    Cytotoxicity against human HEK293 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    Cytotoxicity against human HEK293 cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    [PMID: 32631552]
    HEK293 IC50
    81.74 μM
    Compound: 1
    Antiproliferative activity against HEK293 cells after 48 hrs by MTT assay
    Antiproliferative activity against HEK293 cells after 48 hrs by MTT assay
    [PMID: 29501940]
    HL60/ADR IC50
    0.5 ng/mL
    Compound: Schisandrol A
    TP_TRANSPORTER: inhibition of VCR transport in HL60/ADR cells (overexpression of MRP1)
    TP_TRANSPORTER: inhibition of VCR transport in HL60/ADR cells (overexpression of MRP1)
    [PMID: 17129588]
    HL60/ADR IC50
    3135 ng/mL
    Compound: Schisandrol A
    TP_TRANSPORTER: inhibition of VP-16 transport in HL60/ADR cells (overexpression of MRP1)
    TP_TRANSPORTER: inhibition of VP-16 transport in HL60/ADR cells (overexpression of MRP1)
    [PMID: 17129588]
    HL60/ADR IC50
    54 ng/mL
    Compound: Schisandrol A
    TP_TRANSPORTER: inhibition of DNR transport in HL60/ADR cells (overexpression of MRP1)
    TP_TRANSPORTER: inhibition of DNR transport in HL60/ADR cells (overexpression of MRP1)
    [PMID: 17129588]
    HeLa IC50
    28.56 μM
    Compound: 1
    Antiproliferative activity against human HeLa cells after 48 hrs by MTT assay
    Antiproliferative activity against human HeLa cells after 48 hrs by MTT assay
    [PMID: 29501940]
    HeLa IC50
    5.06 μM
    Compound: 1
    Antiproliferative activity against human HeLa cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    Antiproliferative activity against human HeLa cells assessed as reduction in cell viability measured after 48 hrs by MTT assay
    [PMID: 32631552]
    HeLa IC50
    > 100 μM
    Compound: 5
    Cytotoxicity against human HeLa cells after 72 hrs by MTT assay
    Cytotoxicity against human HeLa cells after 72 hrs by MTT assay
    [PMID: 23237974]
    K562 IC50
    25 μM
    Compound: Schizandrin
    Antiproliferative activity against human K562 cells after 72 hrs by MTT assay
    Antiproliferative activity against human K562 cells after 72 hrs by MTT assay
    [PMID: 18063366]
    MCF7 IC50
    32.56 μM
    Compound: 1
    Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
    Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
    [PMID: 29501940]
    MDA-MB-231 IC50
    61.5 μM
    Compound: Schizandrin
    Antiproliferative activity against human MDA-MB-231 cells after 72 hrs by SRB assay
    Antiproliferative activity against human MDA-MB-231 cells after 72 hrs by SRB assay
    [PMID: 18063366]
    SK-HEP1 IC50
    71.3 μM
    Compound: Schizandrin
    Antiproliferative activity against human SK-HEP1 cells after 72 hrs by SRB assay
    Antiproliferative activity against human SK-HEP1 cells after 72 hrs by SRB assay
    [PMID: 18063366]
    SMMC-7721 IC50
    > 100 μM
    Compound: 5
    Cytotoxicity against human SMMC7721 cells after 72 hrs by MTT assay
    Cytotoxicity against human SMMC7721 cells after 72 hrs by MTT assay
    [PMID: 23237974]
    SNU-638 IC50
    21.1 μM
    Compound: Schizandrin
    Antiproliferative activity against human SNU638 cells after 72 hrs by SRB assay
    Antiproliferative activity against human SNU638 cells after 72 hrs by SRB assay
    [PMID: 18063366]
    T47D IC50
    19.8 μM
    Compound: Schizandrin
    Antiproliferative activity against human T47D cells after 72 hrs by SRB assay
    Antiproliferative activity against human T47D cells after 72 hrs by SRB assay
    [PMID: 18063366]
    U-87MG ATCC IC50
    > 100 μM
    Compound: 5
    Cytotoxicity against human U87 cells after 72 hrs by MTT assay
    Cytotoxicity against human U87 cells after 72 hrs by MTT assay
    [PMID: 23237974]
    体外実験

    Schisandrin (10-100 μM; pretreated for 2 h) inhibits LPS-stimulated NO production, iNOS protein and mRNA expression in a dose-dependent manner in RAW 264.7 cells[1].
    Schisandrin (25-100 μM; pretreated for 2 h) inhibits prostaglandin E2 production, COX-2 protein and mRNA expression in LPS-stimulated RAW 264.7 macrophages[1].
    Schisandrin inhibits the SK-HEP-1, SNU-638, and T47D cells proliferation, with IC50s of 42.0, 53.1, and 40.0 μM, respectively[3].
    Schisandrin (10-60 μM; 48 h) enhances Doxorubicin -induced apoptosis and selectively reverses MCF-7/DOX resistance[4].

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

    Cell Viability Assay[1]

    Cell Line: RAW 264.7 macrophages
    Concentration: 12.5, 25, 50, 100 μM
    Incubation Time: Pretreated for 2 h and then incubated with LPS (1 μg/mL) for 18 h
    Result: Markedly decreased iNOS protein expression a dose-dependent manner.
    Significantly inhibited COX-2 protein expression.
    体内実験

    Schisandrin (10-100 mg/kg; a single i.p.) inhibits acetic acid-induced peritoneal vascular permeability and reduces the carrageenan-induced paw edema of mice[1].
    Schisandrin (1-10 mg/kg; a single p.o.) significantly reverses the Scopolamine-induced impairment of spatial memory and passive avoidance response, and enhances tremors induced by Oxotremorine in rats[2].

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

    Animal Model: Male ICR mice (4-weeks) were treated with λ-carrageenan by intraperitoneal injection into the right hind paw[1]
    Dosage: 100, 200 mg/kg
    Administration: A single i.p.
    Result: Inhibited paw edema by 33.43 % (100 mg/kg) and 57.38 % (200 mg/kg) at 3 h.
    分子量

    432.51

    分子式

    C24H32O7

    CAS 番号
    Appearance

    Solid

    Color

    White to light yellow

    SMILES

    O[C@]1(C)[C@@H](C)CC2=CC(OC)=C(OC)C(OC)=C2C3=C(OC)C(OC)=C(OC)C=C3C1

    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 : 200 mg/mL (462.42 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 2.3121 mL 11.5604 mL 23.1209 mL
    5 mM 0.4624 mL 2.3121 mL 4.6242 mL
    10 mM 0.2312 mL 1.1560 mL 2.3121 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)

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    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    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 0.28 mg/mL (0.65 mM); Clear solution

      This protocol yields a clear solution of ≥ 0.28 mg/mL (saturation unknown).

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (2.8 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.
    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: 99.97%

    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 2.3121 mL 11.5604 mL 23.1209 mL 57.8021 mL
    5 mM 0.4624 mL 2.3121 mL 4.6242 mL 11.5604 mL
    10 mM 0.2312 mL 1.1560 mL 2.3121 mL 5.7802 mL
    15 mM 0.1541 mL 0.7707 mL 1.5414 mL 3.8535 mL
    20 mM 0.1156 mL 0.5780 mL 1.1560 mL 2.8901 mL
    25 mM 0.0925 mL 0.4624 mL 0.9248 mL 2.3121 mL
    30 mM 0.0771 mL 0.3853 mL 0.7707 mL 1.9267 mL
    40 mM 0.0578 mL 0.2890 mL 0.5780 mL 1.4451 mL
    50 mM 0.0462 mL 0.2312 mL 0.4624 mL 1.1560 mL
    60 mM 0.0385 mL 0.1927 mL 0.3853 mL 0.9634 mL
    80 mM 0.0289 mL 0.1445 mL 0.2890 mL 0.7225 mL
    100 mM 0.0231 mL 0.1156 mL 0.2312 mL 0.5780 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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    製品名:
    Schisandrin
    製品番号:
    HY-N0691
    数量:
    MCE 日本正規代理店: