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Liquiritin

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Catalog No. T2899Cas No. 551-15-5
Alias Liquiritoside, Liquiritigenin-4'-O-glucoside

Liquiritin (Liquiritigenin-4'-O-glucoside) (LIQ) is a main component among the licorice flavonoids, and possesses anti-inflammatory and anti-cancer abilities.

Liquiritin

Liquiritin

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Purity: 98.66%
Catalog No. T2899Alias Liquiritoside, Liquiritigenin-4'-O-glucosideCas No. 551-15-5
Liquiritin (Liquiritigenin-4'-O-glucoside) (LIQ) is a main component among the licorice flavonoids, and possesses anti-inflammatory and anti-cancer abilities.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$39In StockIn Stock
10 mg$64In StockIn Stock
25 mg$128In StockIn Stock
50 mg$198In StockIn Stock
100 mg$328In StockIn Stock
500 mg$788-In Stock
1 mL x 10 mM (in DMSO)$43In 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:98.66%
Color:White
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Product Introduction

Liquiritin AI Summary
Liquiritin exhibits a diverse range of bioactivities. It inhibits cow milk xanthine oxidase with an inhibition rate of 18.0% at a concentration of 50 µg/mL. The compound shows inhibition of neuraminidase activity in various Influenza A strains, including the Spanish flu strain A/Bervig_Mission/1/18, with an IC50 value of 82,300.0 nM and a noncompetitive inhibition Ki value of 123,700.0 nM. Additionally, Liquiritin demonstrates inhibitory activities against enzymes such as AmpC Beta-Lactamase, BAZ2B, ELG1-dependent DNA repair, Polymerase Iota, Protein Disulfide Isomerase, and MBNL1-poly(CUG) RNA binding. It shows cytotoxicity against MDCK cells with a CC50 greater than 239,000.0 nM and inhibits neuraminidase of oseltamivir-resistant Influenza A virus H1N1 B/55/08 with an IC50 of 140,000.0 nM and Influenza A virus A/Puerto Rico/8/1934(H1N1) with an IC50 of 83,100.0 nM. The compound exhibits modulatory effects on miRNAs, particularly on miR-21, and shows promising activity in re-activating p53, acting as a general anesthetic, and in beta-arrestin-biased ligand assays for beta2-adrenergic receptor. Furthermore, Liquiritin selectively kills Giardia lamblia, inhibits Marburg Virus entry, induces DNA re-replication in normal breast cells, and has shown antitussive and expectorant activities in ICR mice. However, it exhibits less than 50% inhibition on PTP1B activity at 100 µM concentration..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Liquiritin (Liquiritigenin-4'-O-glucoside) (LIQ) is a main component among the licorice flavonoids, and possesses anti-inflammatory and anti-cancer abilities.
Targets&IC50
AKR1C3:3.72μM (IC50), AKR1C2:0.61 μM (IC50), AKR1C1:0.62 μM (IC50)
SynonymsLiquiritoside, Liquiritigenin-4'-O-glucoside
Chemical Properties
Molecular Weight418.39
FormulaC21H22O9
Cas No.551-15-5
SmilesOC[C@H]1O[C@@H](Oc2ccc(cc2)[C@@H]2CC(=O)c3ccc(O)cc3O2)[C@H](O)[C@@H](O)[C@@H]1O
Relative Density.1.529g/cm3
Storage & Solubility Information
Storagekeep 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
DMSO: 150 mg/mL (358.52 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (9.56 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 mM2.3901 mL11.9506 mL23.9011 mL119.5057 mL
5 mM0.4780 mL2.3901 mL4.7802 mL23.9011 mL
10 mM0.2390 mL1.1951 mL2.3901 mL11.9506 mL
20 mM0.1195 mL0.5975 mL1.1951 mL5.9753 mL
50 mM0.0478 mL0.2390 mL0.4780 mL2.3901 mL
100 mM0.0239 mL0.1195 mL0.2390 mL1.1951 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:
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2 Enter the in vivo formulation:
% DMSO
%
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