1. Cell Cycle/DNA Damage Cytoskeleton Apoptosis
  2. Microtubule/Tubulin Apoptosis
  3. Eribulin mesylate

Eribulin mesylate  (Synonyms: B1939 mesylate; E7389 mesylate; ER-086526 mesylate)

製品番号: HY-13442A 純度: 98.97%
COA 取扱説明書 Technical Support

Eribulin mesylate is an inhibitor for microtubule. Eribulin mesylate inhibits the proliferation of cancer cell LM8 and Dunn, inhibits the cell migration of LM8, arrests the cell cycle at G2/M phase, and induces apoptosis in LM8. Eribulin mesylate exhibits antitumor efficacy in mouse model.

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CAS 番号 : 441045-17-6

容量 価格(税別) 在庫状況 数量
500 μg $120 在庫あり
1 mg $192 在庫あり
5 mg $480 在庫あり
10 mg $768 在庫あり
25 mg $1380 在庫あり
50 mg $1940 在庫あり
100 mg $2720 在庫あり
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500 mg   お問い合わせ  

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カスタマーレビュー

Based on 8 publication(s) in Google Scholar

Other Forms of Eribulin mesylate:

Top Publications Citing Use of Products

    Eribulin mesylate purchased from MedChemExpress. Usage Cited in: Dev Cell. 2025 Mar 25:S1534-5807(25)00151-0.  [Abstract]

    Eribulin (0-210 nM; 72 h). Cell viability of 4T1 S1, R4, and R8 cells following treatments of Eribulin for 72 h.

    Eribulin mesylate purchased from MedChemExpress. Usage Cited in: NPJ Breast Cancer. 2025 Feb 17;11(1):17.  [Abstract]

    Eribulin (1 nM; 72 h). Microscopic images of EdU (pink) and DAPI (blue) channels for two selected models: HBCx-4B and HBCx-39.

    Eribulin mesylate purchased from MedChemExpress. Usage Cited in: NPJ Breast Cancer. 2025 Feb 17;11(1):17.  [Abstract]

    Eribulin (1 nM; 72 h). Quantification of HBCx-4B and HBCx-39 TUNEL staining. Each data point represents quantification of the percentage of cells in apoptosis within one microscopic field of view; ten fields of view were analyzed per condition in triplicate.

    Eribulin mesylate purchased from MedChemExpress. Usage Cited in: NPJ Breast Cancer. 2025 Feb 17;11(1):17.  [Abstract]

    Eribulin (0.4 mg/kg; IV). Results of the in vivo eribulin treatment of the HBCx-137 PDX model, representing the measurements of the tumor size in mm3 over the time in culture.

    Eribulin mesylate purchased from MedChemExpress. Usage Cited in: NPJ Breast Cancer. 2025 Feb 17;11(1):17.  [Abstract]

    Eribulin (1 nM; 72 h). Representative images of the pH3- (green) and EdU-positive (pink) cells with and without Eribulin treatment for the HBCx-137 PDX model (Eribulin-sensitive in vivo).
    • 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

    Eribulin mesylate is an inhibitor for microtubule. Eribulin mesylate inhibits the proliferation of cancer cell LM8 and Dunn, inhibits the cell migration of LM8, arrests the cell cycle at G2/M phase, and induces apoptosis in LM8. Eribulin mesylate exhibits antitumor efficacy in mouse model[1].

    Cellular Effect
    Cell Line Type Value Description References
    MES-SA IC50
    1.66 1
    Compound: Halaven
    Antiproliferative activity against human MES-SA cells
    Antiproliferative activity against human MES-SA cells
    [PMID: 21324687]
    MES-SA IC50
    1.66 1
    Compound: Halaven
    Antiproliferative activity against human MES-SA cells
    Antiproliferative activity against human MES-SA cells
    [PMID: 21324687]
    MES-SA IC50
    1.7 1
    Compound: 1
    Cytotoxicity against human MES-SA cells
    Cytotoxicity against human MES-SA cells
    [PMID: 23141916]
    MES-SA IC50
    1.7 1
    Compound: 1
    Cytotoxicity against human MES-SA cells
    Cytotoxicity against human MES-SA cells
    [PMID: 23141916]
    SF-295 IC50
    27.85 1
    Compound: Halaven
    Antiproliferative activity against human SF295 cells
    Antiproliferative activity against human SF295 cells
    [PMID: 21324687]
    U-251 IC50
    5.87 1
    Compound: Halaven
    Antiproliferative activity against human U251 cells
    Antiproliferative activity against human U251 cells
    [PMID: 21324687]
    SF-295 IC50
    27.85 1
    Compound: Halaven
    Antiproliferative activity against human SF295 cells
    Antiproliferative activity against human SF295 cells
    [PMID: 21324687]
    U-251 IC50
    5.87 1
    Compound: Halaven
    Antiproliferative activity against human U251 cells
    Antiproliferative activity against human U251 cells
    [PMID: 21324687]
    体外実験

    Eribulin mesylate (1-100 nM; 72 h) inhibits cells proliferation, with IC50s of 22.8 and 21.5 nM for LM8 and Dunn cells, respectively[1].
    Eribulin mesylate (10-50 nM; 12-72 h) increases early apoptosis significantly after 24 h treatment at the dose of 50 nM in LM8 cells[1].
    Eribulin mesylate (10-50 nM; 12-72 h) induces G2/M arrest by 12 h treatment with at the dose of 50 nM, but not by long-term treatment (72 h) with 10 nM in LM8 cells[1].
    Eribulin mesylate (1-50 nM; 12 h) does not induce senescence in LM8 cells[1].
    Eribulin mesylate (1-10 nM; 16 h) induces morphological change and suppresses cell migration in a low concentration in LM8 cells[1].

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

    Cell Proliferation Assay[1]

    Cell Line: LM8 cells and Dunn cells
    Concentration: 0, 1, 10, 100 nM
    Incubation Time: 72 hours
    Result: Inhibited cells proliferation in a dose-dependent manner.

    Apoptosis Analysis[1]

    Cell Line: LM8 cells
    Concentration: 0, 10, 50 nM
    Incubation Time: 12, 24, 48, 72 hour
    Result: Induced early apoptosis after 12 h at the concentration of 50 nM.
    Not detected apoptosis at the concentration of 10 nM.

    Cell Cycle Analysis[1]

    Cell Line: LM8 cells
    Concentration: 0, 10, 50 nM
    Incubation Time: 12, 24, 48, 72 hour
    Result: Induced G2/M arrest by 12 h treatment with 50 nM.
    No G2/M arrest was induced by10 nM treatment.
    体内実験

    Eribulin mesylate (1 mg/kg; i.v. once a week for 2 weeks) reduces primary tumor growth and lung metastasis of osteosarcoma in mice[1].
    Eribulin mesylate (1 mg/kg; once i.v.) suppresses circulating tumor cells (CTC) appearance in the low-concentration phase[1].

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

    Animal Model: C3H/HeN mice (4-week-old) are injected LM8 cells[1]
    Dosage: 1 mg/kg
    Administration: I.v. once a week for 2 weeks
    Result: Suppressed primary tumor growth and induced apoptosis in tumor cells.
    Reduced lung metastasis.
    分子量

    826.00

    分子式

    C41H63NO14S

    CAS 番号
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    C=C1C[C@@](CC[C@@]2(C[C@@]3([H])O4)O[C@]([C@](O[C@](C5)([H])CC6)([H])[C@@]6([H])O7)([H])[C@@]4([H])[C@]7([H])[C@@]3([H])O2)([H])O[C@@]1([H])CC[C@](C[C@@H](C)C8=C)([H])O[C@]8([H])C[C@@](O[C@H](C[C@H](O)CN)[C@@H]9OC)([H])[C@]9([H])CC5=O.CS(=O)(O)=O

    輸送条件

    Shipping with dry ice.

    保管条件

    -80°C, sealed storage, away from moisture and light

    溶剤 & 溶解度
    体外: 

    DMSO : ≥ 100 mg/mL (121.07 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    *"≥" means soluble, but saturation unknown.

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.2107 mL 6.0533 mL 12.1065 mL
    5 mM 0.2421 mL 1.2107 mL 2.4213 mL
    10 mM 0.1211 mL 0.6053 mL 1.2107 mL
    View the Complete Stock Solution Preparation Table
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    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: ≥ 2.5 mg/mL (3.03 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 (3.03 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.
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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).
    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: 99.91%

    参考文献

    Complete Stock Solution Preparation Table

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 1.2107 mL 6.0533 mL 12.1065 mL 30.2663 mL
    5 mM 0.2421 mL 1.2107 mL 2.4213 mL 6.0533 mL
    10 mM 0.1211 mL 0.6053 mL 1.2107 mL 3.0266 mL
    15 mM 0.0807 mL 0.4036 mL 0.8071 mL 2.0178 mL
    20 mM 0.0605 mL 0.3027 mL 0.6053 mL 1.5133 mL
    25 mM 0.0484 mL 0.2421 mL 0.4843 mL 1.2107 mL
    30 mM 0.0404 mL 0.2018 mL 0.4036 mL 1.0089 mL
    40 mM 0.0303 mL 0.1513 mL 0.3027 mL 0.7567 mL
    50 mM 0.0242 mL 0.1211 mL 0.2421 mL 0.6053 mL
    60 mM 0.0202 mL 0.1009 mL 0.2018 mL 0.5044 mL
    80 mM 0.0151 mL 0.0757 mL 0.1513 mL 0.3783 mL
    100 mM 0.0121 mL 0.0605 mL 0.1211 mL 0.3027 mL
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    一般には略語で表示されます:C1V1 = C2V2

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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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    製品名:
    Eribulin mesylate
    製品番号:
    HY-13442A
    数量:
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