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Menbutone

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Catalog No. T1148Cas No. 3562-99-0
Alias Naftobil, Genabilin, Genabilic acid

Menbutone (Genabilin) is a derivative of oxobutyric acid, and is a choleretic. Menbutone shows a rapid onset of action, reaching its maximum plasma level within 1 hour and lasting for roughly 10 hours.

Menbutone

Menbutone

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Purity: 97.48%
Catalog No. T1148Alias Naftobil, Genabilin, Genabilic acidCas No. 3562-99-0
Menbutone (Genabilin) is a derivative of oxobutyric acid, and is a choleretic. Menbutone shows a rapid onset of action, reaching its maximum plasma level within 1 hour and lasting for roughly 10 hours.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
100 mg$30In StockIn Stock
500 mg$60-In Stock
1 g$79-In Stock
1 mL x 10 mM (in DMSO)$30In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:97.48%
Appearance:Solid
Color:White
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Product Introduction

Menbutone AI Summary
Menbutone shows bioactivity related to the S16 Schwann cell PMP22 intronic element firefly luciferase assay with a potency of 642.4 nM. Additionally, it exhibits antiviral activity against SARS-CoV-2, providing a mixed inhibition profile. In Caco-2 cells, it inhibits virus-induced cytotoxicity by 1.94% at 10 µM after 48 hours. In HRCE cells, the compound showed a low level of activity with a hit score of 0.04313 against the USA-WA1/2020 strain at MOI 0.4 over 96 hours. In VERO-6 cells, at the same concentration and time period, it achieved an inhibition percentage of 0.04%. Menbutone also inhibits the SARS-CoV-2 3CL-Pro protease by 11.97% at 20 µM based on a FRET response from a peptide substrate. Furthermore, it shows inhibition of human HDAC6 activity, with an inhibition of 0.61% in an enzymatic assay using a commercial peptide substrate, while showing -8.25% inhibition with a custom peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Menbutone (Genabilin) is a derivative of oxobutyric acid, and is a choleretic. Menbutone shows a rapid onset of action, reaching its maximum plasma level within 1 hour and lasting for roughly 10 hours.
SynonymsNaftobil, Genabilin, Genabilic acid
Chemical Properties
Molecular Weight258.27
FormulaC15H14O4
Cas No.3562-99-0
SmilesC(CCC(O)=O)(=O)C=1C2=C(C(OC)=CC1)C=CC=C2
Relative Density.1.249 g/cm3
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: 50 mg/mL (193.6 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (7.74 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 mM3.8719 mL19.3596 mL38.7192 mL193.5958 mL
5 mM0.7744 mL3.8719 mL7.7438 mL38.7192 mL
10 mM0.3872 mL1.9360 mL3.8719 mL19.3596 mL
20 mM0.1936 mL0.9680 mL1.9360 mL9.6798 mL
50 mM0.0774 mL0.3872 mL0.7744 mL3.8719 mL
100 mM0.0387 mL0.1936 mL0.3872 mL1.9360 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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Tech Support

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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