Methyl-β-cyclodextrin (MβCD)

Synonyms: Methyl-beta-cyclodextrin, M-β-CyD, Methyl-β-CD

Methyl-β-cyclodextrin (MβCD) is a cholesterol-removing agent mainly used for lipid raft disruption. Methyl-β-cyclodextrin induces caspase-dependent apoptosis in PEL cells and inhibits the growth and invasion of PEL cells without apparent adverse effects, suggesting the potential effective antitumor activities.

Methyl-β-cyclodextrin (MβCD) Chemical Structure

Methyl-β-cyclodextrin (MβCD) Chemical Structure

CAS: 128446-36-6

Selleck's Methyl-β-cyclodextrin (MβCD) has been cited by 11 publications

Purity & Quality Control

Batch: S682701 Purity: 98%
98

Methyl-β-cyclodextrin (MβCD) Related Products

Biological Activity

Description Methyl-β-cyclodextrin (MβCD) is a cholesterol-removing agent mainly used for lipid raft disruption. Methyl-β-cyclodextrin induces caspase-dependent apoptosis in PEL cells and inhibits the growth and invasion of PEL cells without apparent adverse effects, suggesting the potential effective antitumor activities.
Targets
cholesterol [1] lipid raft [1]
In vitro
In vitro

Methyl-β-cyclodextrin Inhibits SDF-1α-induced platelet aggregation and Akt phosphorylation by raft disruption.[2]

Cell Research Cell lines Platelets
Concentrations 2%
Incubation Time 15 min
Method

Freshly isolated human platelets are incubated with SDF-1α and centrifuged for 1 min at 3000 rpm. The resulting pellet is resuspended and boiled in Laemmli sample buffer containing phosphatase inhibitor cocktails 2 and 3. Phosphorylations of Akt (Ser473) is detected by western blotting. Platelet aggregation is measured as the optical density of PRP during aggregation using a platelet aggregometer, with the platelet-poor plasma 100% standard for change in optical density.

In Vivo
In vivo

In a Primary effusion lymphoma (PEL) xenograft mouse model, Methyl-β-cyclodextrin significantly inhibits the growth and invasion of PEL cells without apparent adverse effects. Methyl-β-cyclodextrin-treated mice appears to be healthy, whereas non-treated mice has a distended abdominal region. The body weights of control are significantly higher than those of Methyl-β-cyclodextrin treated mice. Methyl-β-cyclodextrin-treated mice has a significantly lower volume of ascites than that of non-treated mice.[1]

Chemical Information & Solubility

Molecular Weight Formula
CAS No. 128446-36-6 SDF --
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

Water : 100 mg/mL


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In vivo
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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.

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