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Mebendazole Parasite inhibitor

Cat.No.S4610

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.
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Quality Control

Batch: Purity: 99.99%
99.99

Solubility

In vitro
Batch:

DMSO : 8 mg/mL (27.09 mM) Warmed with 60°C water bath; Ultrasonicated;
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
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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.

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Chemical Information, Storage & Stability

Molecular Weight 295.29 Formula

C16H13N3O3

Storage (From the date of receipt)
CAS No. 31431-39-7 Download SDF Storage of Stock Solutions

Synonyms Mebenvet SMILES COC(=O)NC1=NC2=C(N1)C=C(C=C2)C(=O)C3=CC=CC=C3

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Mechanism of Action

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.
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.
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2019-04-24)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT03925662 RECRUITING
Colorectal Cancer
Sherief Abd-Elsalam
2019-04-01 PHASE3
NCT06800248 NOT_YET_RECRUITING
Trichuris Trichiura; Infection; Hookworm Infection; Ascaris Lumbricoides Infection
Swiss Tropical & Public Health Institute
2026-11-06 PHASE3
NCT01837862 ACTIVE_NOT_RECRUITING
Pilomyxoid Astrocytoma; Pilocytic Astrocytoma; Glioma, Astrocytic; Optic Nerve Glioma; Pleomorphic Xanthoastrocytoma; Glioblastoma Multiforme; Anaplastic Astrocytoma; Gliosarcoma; Diffuse Intrinsic Pontine Glioma; DIPG; Low-grade Glioma; Brainstem Glioma
Julie Krystal
2013-10-22 PHASE1; PHASE2
NCT06736691 ACTIVE_NOT_RECRUITING
Trichuris Trichiura; Infection; Hookworm Infection; Ascaris Lumbricoides Infection
Swiss Tropical & Public Health Institute
2025-11-25 PHASE3
NCT06335160 RECRUITING
Ulcerative Colitis
Tanta University
2024-04-20
NCT06720259 COMPLETED
Trichuris Trichiura; Infection; Hookworm Infection; Ascaris Lumbricoides Infection
Jennifer Keiser
2025-04-16 PHASE2

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