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Eribulin Mesylate Microtubule Associated inhibitor

Cat.No.S8912

Eribulin Mesylate, an analogue of the marine natural product halichondrin B, is a nontaxane completely synthetic microtubule inhibitor.
Eribulin Mesylate Microtubule Associated inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 826

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 826 Formula

C41H63NO14S

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 441045-17-6 -- Storage of Stock Solutions

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (121.06 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 100 mg/mL

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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In vivo Formulation Calculator (Clear solution)

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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Mechanism of Action

Targets/IC50/Ki
microtubule [1]
In vitro

Eribulin Mesylate (1-100 nM; 72 h) inhibits cells proliferation of LM8 and Dunn cells. This compound (10-50 nM; 12-72 h) increases early apoptosis significantly in LM8 cells. It (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. This chemical (1-10 nM; 16 h) induces morphological change and suppresses cell migration in a low concentration in LM8 cells.[2]

In vivo

Eribulin Mesylate reduces primary tumor growth and lung metastasis of osteosarcoma in mice.[2]

References

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