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3-Methyltoxoflavin

Catalog No.GC33060

La 3-méthyltoxoflavine est un puissant inhibiteur de la protéine disulfure isomérase (PDI), avec une IC50 de 170 nM.

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3-Methyltoxoflavin Chemical Structure

Cas No.: 32502-62-8

Taille Prix Stock Qté
10mM (in 1mL DMSO)
116,00 $US
En stock
1mg
51,00 $US
En stock
5mg
120,00 $US
En stock
10mg
180,00 $US
En stock
25mg
314,00 $US
En stock
50mg
456,00 $US
En stock

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Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

Description of 3-Methyltoxoflavin

3-Methyltoxoflavin is a potent Protein disulfide isomerase (PDI) inhibitor, with an IC50 of 170 nM.

3-Methyltoxoflavin is a potent Protein disulfide isomerase (PDI) inhibitor, with an IC50 of 170 nM. 3-Methyltoxoflavin is toxic in a panel of human glioblastoma cell lines. From the screen, 3-Methyltoxoflavin emerges as the most cytotoxic inhibitor of PDI. Bromouridine labeling and sequencing (Bru-seq) of nascent RNA reveals that 3-Methyltoxoflavin induces Nrf2 antioxidant response, ER stress response, and autophagy. Specifically, 3-Methyltoxoflavin upregulates heme oxygenase 1 and SLC7A11 transcription and protein expression and represses PDI target genes such as TXNIP and EGR1. Interestingly, 3-Methyltoxoflavin-induced cell death does not proceed via apoptosis or necrosis, but by a mixture of autophagy and ferroptosis[1].

[1]. Kyani A, et al. Discovery and Mechanistic Elucidation of a Class of Protein Disulfide Isomerase Inhibitors for the Treatment of Glioblastoma. ChemMedChem. 2018 Jan 22;13(2):164-177.

Protocol of 3-Methyltoxoflavin

Cell experiment:

The colon cancer cells are seeded in duplicate in 96-well plates at 7000-10000 cells per well. For the combination therapies, NAC is added to the well at the same time as 3-Methyltoxoflavin (35G8) (24 hours after plates are seeded), and Z-VAD-FMK and Necrostatin-1 are added to the well 1 hour prior to 3-Methyltoxoflavin addition. Cell growth inhibition is assessed by the cell viability rate. Cell viability is determined with the MTT assay. U87MG cells are seeded at 5000 cells per well in 96-well plates. Deferoxamine is added to cells in a five-point, three-fold dilution series from 400 μM. 3-Methyltoxoflavin is added immediately after in a five-point, three-fold dilution series from 100 μM. Cells are incubated with compounds for 12 hours[1].

References:

[1]. Kyani A, et al. Discovery and Mechanistic Elucidation of a Class of Protein Disulfide Isomerase Inhibitors for the Treatment of Glioblastoma. ChemMedChem. 2018 Jan 22;13(2):164-177.

Chemical Properties of 3-Methyltoxoflavin

Cas No. 32502-62-8 SDF
Canonical SMILES CC1=NN(C)C(C2=N1)=NC(N(C)C2=O)=O
Formula C8H9N5O2 M.Wt 207.19
Solubility DMSO : 150 mg/mL (723.97 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of 3-Methyltoxoflavin

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 4.8265 mL 24.1324 mL 48.2649 mL
5 mM 965.3 μL 4.8265 mL 9.653 mL
10 mM 482.6 μL 2.4132 mL 4.8265 mL
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Review for 3-Methyltoxoflavin

Average Rating: 5 ★★★★★ (Based on Reviews and 22 reference(s) in Google Scholar.)

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