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Mulberroside F

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Catalog No. TN1958Cas No. 193483-95-3

Mulberroside F, a natural product isolated from Morus alba L., inhibits melanin biosynthesis and associated tyrosinase activity while scavenging superoxide and preventing autooxidation.

Mulberroside F

Mulberroside F

😃Good
Purity: 99.98%
Catalog No. TN1958Cas No. 193483-95-3
Mulberroside F, a natural product isolated from Morus alba L., inhibits melanin biosynthesis and associated tyrosinase activity while scavenging superoxide and preventing autooxidation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$64-In Stock
5 mg$172-In Stock
10 mg$272-In Stock
25 mg$458-In Stock
50 mg$663-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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Batch Information

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Purity:99.98%
Appearance:Solid
Color:Green
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Product Introduction

Bioactivity
Description
Mulberroside F, a natural product isolated from Morus alba L., inhibits melanin biosynthesis and associated tyrosinase activity while scavenging superoxide and preventing autooxidation.
In vitro
Mulberroside F (IC50=0.29 μg/ml) and Kojic acid (IC50=1.30 μg/mL) both exhibited strong inhibitory activity against tyrosinase. After treatment with Mulberroside F, the tyrosinase activity in the HM3KO cell line also showed a decreasing trend, and this trend correlated with the inhibition pattern of Agaricus campestris tyrosinase. Mulberroside F (68.3 μg/mL) could inhibit mammalian tyrosinase activity by 50% [1].
Chemical Properties
Molecular Weight566.51
FormulaC26H30O14
Cas No.193483-95-3
SmilesO(C=1C=C(C=2OC=3C(C2)=CC=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C3)C=C(O)C1)[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O
Relative Density.1.645 g/cm3 (Predicted)
Storage & Solubility Information
Storagekeep away from moisture,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Ethanol: 4 mg/mL (7.06 mM), Sonication is recommended.
Solution Preparation Table
Ethanol
1mg5mg10mg50mg
1 mM1.7652 mL8.8260 mL17.6519 mL88.2597 mL
5 mM0.3530 mL1.7652 mL3.5304 mL17.6519 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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