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Eribulin mesylate

(Synonyms: ER-086526 mesylate, E7389 mesylate, B1939 mesylate) Copy Product Info
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Synonyms: ER-086526 mesylate, E7389 mesylate, B1939 mesylate

Catalog No. T13687 Copy Product Info
Purity: 99.89%
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Eribulin mesylate (E7389 mesylate) belongs to natural product derivatives and is a microtubule-targeted anticancer agent, functioning as a microtubule dynamics inhibitor that suppresses tubulin polymerization through tubulin binding, with cell permeability. This drug is used for the treatment of metastatic breast cancer.
Eribulin mesylate
Cas No. 441045-17-6
Pack SizePriceUSA StockGlobal StockQuantity
500 μg$98In StockIn Stock
1 mg$157In StockIn Stock
2 mg$233In StockIn Stock
5 mg$396In StockIn Stock
10 mg$635In StockIn Stock
25 mg$1,130In StockIn Stock
50 mg$1,580In StockIn Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.89%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Eribulin mesylate (E7389 mesylate) belongs to natural product derivatives and is a microtubule-targeted anticancer agent, functioning as a microtubule dynamics inhibitor that suppresses tubulin polymerization through tubulin binding, with cell permeability. This drug is used for the treatment of metastatic breast cancer.
Targets & IC50
LM8 cells:22.8 nM, MDA-MB-435 cells:0.09 nM, Dunn cells:21.5 nM
In vitro
Methods:Seventeen small cell lung cancer cell lines were incubated with 0–10 nM Eribulin mesylate for 5 days. In vitro activity was evaluated by MTS assay, flow cytometry, and Caspase-Glo 3/7 assay.
Results: Eribulin mesylate concentration-dependently inhibited proliferation in all cell lines, with IC₅₀ values of 1–6 nM and inhibition rates of 53%–98% at 10 nM, while inducing G2/M phase arrest and apoptosis.[1]
Methods: Human pancreatic cancer AsPC-1, Panc-1, SUIT-2 cells and human pancreatic endoderm hPE cells were used to evaluate Eribulin mesylate in vitro activity by WST assay (incubation concentration 0.5–10 ng/mL, treatment for 90 min) and morphological observation (treatment for 24 h).
Results: Eribulin mesylate significantly and concentration-dependently inhibited viability of AsPC-1 and Panc-1 cells, inducing morphological changes including cell shrinkage and membrane blebbing, but had no effect on hPE cells.[2]
In vivo
Methods: Subcutaneous xenograft models of human leiomyosarcoma SK-LMS-1, liposarcoma SW 872, Ewing sarcoma A-673, and fibrosarcoma HT-1080 were established in Balb/c-nu mice. Eribulin mesylate was administered intravenously at doses of 0.875–3.5 mg/kg once every 7 days (q7d×1 or ×2), with normal saline as the control.
Results: Eribulin mesylate demonstrated significant antitumor activity, with tumor regression observed in all models and good tolerability.[3]
SynonymsER-086526 mesylate, E7389 mesylate, B1939 mesylate
Chemical Properties
Molecular Weight826
FormulaC41H63NO14S
Cas No.441045-17-6
SmilesCS(O)(=O)=O.[H][C@@]12CC(=C)[C@]([H])(CC[C@@]3([H])C[C@@H](C)C(=C)[C@@]([H])(C[C@]4([H])O[C@H](C[C@H](O)CN)[C@H](OC)[C@@]4([H])CC(=O)C[C@@]4([H])CC[C@]5([H])O[C@@]6([H])[C@@]7([H])O[C@@]8(C[C@@]7([H])O[C@@]6([H])[C@@]([H])(O8)[C@@]5([H])O4)CC1)O3)O2
Relative Density.no data available
Storage & Solubility Information
StorageStore at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Ethanol: 98 mg/mL (118.64 mM), Sonication is recommended.
DMSO: 255 mg/mL (308.72 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (6.05 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM1.2107 mL6.0533 mL12.1065 mL60.5327 mL
5 mM0.2421 mL1.2107 mL2.4213 mL12.1065 mL
10 mM0.1211 mL0.6053 mL1.2107 mL6.0533 mL
20 mM0.0605 mL0.3027 mL0.6053 mL3.0266 mL
50 mM0.0242 mL0.1211 mL0.2421 mL1.2107 mL
100 mM0.0121 mL0.0605 mL0.1211 mL0.6053 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Keywords

Related Tags: Eribulin mesylate chemical structure | Eribulin mesylate in vivo | Eribulin mesylate in vitro | Eribulin mesylate formula | Eribulin mesylate molecular weight