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Mebendazole Parasite inhibitor

Mebendazole is a synthetic benzimidazole derivate and anthelmintic agent. This compound interferes with the reproduction and survival of helminths by inhibiting the formation of their cytoplasmic microtubules, thereby selectively and irreversibly blocking glucose uptake.

Mebendazole Parasite inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 295.29

Purity & Quality Control

Related Products

Mechanism of Action

In vitro

In vitro mebendazole (MZ), a derivative of benzimidazole, induces a dose- and time-dependent apoptotic response in human lung cancer cell lines. This compound arrests cells at the G2-M phase before the onset of apoptosis. Its treatment also results in mitochondrial cytochrome c release, followed by apoptotic cell death. Additionally, this chemical appears to be a potent inhibitor of tumor cell growth with little toxicity to normal WI38 and human umbilical vein endothelial cells[2].
Cell Research Cell lines A549, WI38 normal fibroblasts, H1299 and H460 cancer cell line
Concentrations 0, 0.2, 0.5, 1 μM
Incubation Time 48 h
Method When grown to 40–50% confluence, the cells are exposed to Mebendazole dissolved in DMSO. Cell growth is monitored by counting the viable cells using a hemacytometer.

In Vivo

In vivo When administered p.o. to nu/nu mice, Mebendazole strongly inhibits the growth of human tumor xenografts and significantly reduces the number and size of tumors in an experimental model of lung metastasis. This compound treatment significantly reduces vessel densities in mice compared with those in control mice[2].
Animal Research Animal Models Mice
Dosages 12.5 and 25 mg/kg/day
Administration oral administration

References

  • https://pubmed.ncbi.nlm.nih.gov/25773183/
  • https://pubmed.ncbi.nlm.nih.gov/12231542/

Chemical Information

Molecular Weight 295.29 Formula

C16H13N3O3

CAS No. 31431-39-7 SDF Download SDF
Synonyms Mebenvet
Smiles COC(=O)NC1=NC2=C(N1)C=C(C=C2)C(=O)C3=CC=CC=C3

Storage and Stability

Storage (From the date of receipt)

In vitro
Batch:

DMSO : 8 mg/mL ( (27.09 mM) Warmed with 50°C water bath; Ultrasonicated; Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble


Molecular Weight Calculator

In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

Preparing Stock Solutions

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO % % Tween 80 % ddH2O
%DMSO %

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Working concentration: mg/ml;

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.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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