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Urolithin M5

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Catalog No. T84318Cas No. 91485-02-8
Alias Decarboxyellagic acid

Urolithin M5 (Decarboxyellagic acid) is a neuraminidase inhibitor isolated from olive leaves with antiviral and anticancer and antitumor activities. Urolithin M5 can be used to study influenza A virus infection and SARS-CoV-2 infection.

Urolithin M5

Urolithin M5

😃Good
Purity: 95.32%
Catalog No. T84318Alias Decarboxyellagic acidCas No. 91485-02-8
Urolithin M5 (Decarboxyellagic acid) is a neuraminidase inhibitor isolated from olive leaves with antiviral and anticancer and antitumor activities. Urolithin M5 can be used to study influenza A virus infection and SARS-CoV-2 infection.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$56In StockIn Stock
5 mg$163In StockIn Stock
10 mg$243In StockIn Stock
25 mg$397-In Stock
50 mg$598-In Stock
100 mg$848-In Stock
200 mg$1,130-In 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:95.32%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Urolithin M5 (Decarboxyellagic acid) is a neuraminidase inhibitor isolated from olive leaves with antiviral and anticancer and antitumor activities. Urolithin M5 can be used to study influenza A virus infection and SARS-CoV-2 infection.
Targets&IC50
MDCK cells:CC50=227.4 μM, Virus:3.74~16.51 μM
In vitro
The cytotoxicity of urolithin M5 was initially assessed using the MTT assay on MDCK cells. Urolithin M5 had a CC50 value of 227.4 μM. [1]
25 μM urolithin M5 inhibited all virus growth, urolithin M5 was the most effective compound, with an IC50 ranging from 3.74 to 16.51 μM. [1]
In vivo
Specific-pathogen-free female BALB/c mice weighing 16 to 18 g. A total of 200 mg/kg/d urolithin M5 treatment improved the survival rate to 50%, which was significantly higher than the vehicle group. These results indicated that 200 mg/kg/d urolithin M5 had a protective effect on PR8-infected mice. [1]
SynonymsDecarboxyellagic acid
Chemical Properties
Molecular Weight276.2
FormulaC13H8O7
Cas No.91485-02-8
SmilesO=C1OC=2C(O)=C(O)C=CC2C3=C(O)C(O)=C(O)C=C13
Relative Density.1.894 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature,keep away from moisture,keep away from direct sunlight | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 15 mg/mL (54.31 mM), Sonication and heating are recommended.
DMSO: 62 mg/mL (224.48 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM3.6206 mL18.1028 mL36.2056 mL181.0282 mL
5 mM0.7241 mL3.6206 mL7.2411 mL36.2056 mL
10 mM0.3621 mL1.8103 mL3.6206 mL18.1028 mL
20 mM0.1810 mL0.9051 mL1.8103 mL9.0514 mL
50 mM0.0724 mL0.3621 mL0.7241 mL3.6206 mL
DMSO
1mg5mg10mg50mg
100 mM0.0362 mL0.1810 mL0.3621 mL1.8103 mL

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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:
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2 Enter the in vivo formulation:
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