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Verubulin hydrochloride

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Catalog No. T13298Cas No. 917369-31-4
Alias MPC-6827 hydrochloride

Verubulin hydrochloride (MPC-6827 hydrochloride) is a blood-brain barrier permeable microtubule-disrupting agent with potent and broad-spectrum cytotoxic activities and significant anticancer efficacy in human MX-1 breast cancer and various mouse xenograft cancer models.

Verubulin hydrochloride

Verubulin hydrochloride

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🥰Excellent
Purity: 99.77%
Catalog No. T13298Alias MPC-6827 hydrochlorideCas No. 917369-31-4
Verubulin hydrochloride (MPC-6827 hydrochloride) is a blood-brain barrier permeable microtubule-disrupting agent with potent and broad-spectrum cytotoxic activities and significant anticancer efficacy in human MX-1 breast cancer and various mouse xenograft cancer models.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$46In StockIn Stock
10 mg$71In StockIn Stock
25 mg$148In StockIn Stock
50 mg$222In StockIn Stock
100 mg$316In StockIn Stock
200 mg$457In StockIn Stock
1 mL x 10 mM (in DMSO)$51In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.77%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Verubulin hydrochloride AI Summary
Verubulin hydrochloride shows significant antitumor activity against human A549 cells xenografted in Balb/c mice, achieving a tumor growth inhibition (TGI) of 68.62% at a dose of 2.5 mg/kg administered via intraperitoneal injection every other day for 10 days. However, in terms of toxicity, the maximum tolerated dose (MTD) in mice is 1.0 mg/kg. Additionally, Verubulin hydrochloride exhibits antiviral activity against SARS-CoV-2. It inhibits the cytotoxicity of SARS-CoV-2 in Caco-2 cells and VERO-6 cells, with inhibition percentages of 50.91% and 0.61% at a concentration of 10 µM, respectively, after 48 hours. The compound also demonstrates bioactivity against the SARS-CoV-2 3CL-Pro protease, showing 12.51% inhibition at 20 µM concentration..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Verubulin hydrochloride (MPC-6827 hydrochloride) is a blood-brain barrier permeable microtubule-disrupting agent with potent and broad-spectrum cytotoxic activities and significant anticancer efficacy in human MX-1 breast cancer and various mouse xenograft cancer models.
SynonymsMPC-6827 hydrochloride
Chemical Properties
Molecular Weight315.8
FormulaC17H18ClN3O
Cas No.917369-31-4
SmilesCl.COc1ccc(cc1)N(C)c1nc(C)nc2ccccc12
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 22.5 mg/mL (71.25 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (6.33 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1666 mL15.8328 mL31.6656 mL158.3281 mL
5 mM0.6333 mL3.1666 mL6.3331 mL31.6656 mL
10 mM0.3167 mL1.5833 mL3.1666 mL15.8328 mL
20 mM0.1583 mL0.7916 mL1.5833 mL7.9164 mL
50 mM0.0633 mL0.3167 mL0.6333 mL3.1666 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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