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Ligupurpuroside B
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Catalog No. TN1869Cas No. 147396-02-9
Ligupurpuroside B is a natural phenethyl glycoside discovered in Ligustrum robustum, exhibiting antioxidant activity with an IC50 of 80.4 μM against AAPH-induced haemolysis.
Ligupurpuroside B
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Purity: 99.95%
Catalog No. TN1869Cas No. 147396-02-9
Ligupurpuroside B is a natural phenethyl glycoside discovered in Ligustrum robustum, exhibiting antioxidant activity with an IC50 of 80.4 μM against AAPH-induced haemolysis.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $172 | - | In Stock | |
| 5 mg | $425 | - | In Stock | |
| 10 mg | $630 | - | In Stock | |
| 25 mg | $983 | - | In Stock | |
| 50 mg | $1,350 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.95%
Appearance:Solid
Color:White
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Product Introduction
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Chemical Properties
Storage & Solubility Information
| Description | Ligupurpuroside B is a natural phenethyl glycoside discovered in Ligustrum robustum, exhibiting antioxidant activity with an IC50 of 80.4 μM against AAPH-induced haemolysis. |
| In vitro | According to Stern-Volmer equation, fluorescence of lipase was quenched by Ligupurpuroside B via a static quenching mechanism because of formation of Ligupurpuroside B-lipase complex. Binding constants, number of binding sites & thermodynamic parameters were evaluated. The values of ΔGo (-25.085 kJ mol-1), ΔHo (-12.14 kJ mol-1) and ΔSo (+43.45 J mol-1 K-1) at 298 K indicated that Ligupurpuroside B-lipase interaction is spontaneous and hydrophobic interaction is the main force stabilizing the Ligupurpuroside B-lipase complex. The enzyme activity assay showed that Ligupurpuroside B inhibited lipase activity efficiently. Synchronous fluorescence spectra (SFS) suggested that Ligupurpuroside B is closer to Trp residues than to Tyr residues.[1] |
| Molecular Weight | 738.74 |
| Formula | C35H46O17 |
| Cas No. | 147396-02-9 |
| Smiles | CC1OC(OC2C(C)OC(OC3C(O)C(OCCc4ccc(O)cc4)OC(CO)C3OC(=O)C=Cc3ccc(O)cc3)C(O)C2O)C(O)C(O)C1O |w:33.34| |
| Relative Density. | 1.53 g/cm3 at 20℃ |
| Storage | keep away from direct sunlight,keep away from moisture,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
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