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Isoliquiritin

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Catalog No. T5S0331Cas No. 5041-81-6
Alias Neoisoliquritin

1. Isoliquiritin (Neoisoliquritin) has antitussive effects. 2. Isoliquiritin has antidepressant-like effects. 3. Isoliquiritin, liquiritin and isoliquirigenin inhibits the p53-dependent pathway and shows crosstalk between Akt activities.

Isoliquiritin

Isoliquiritin

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Purity: 99.88%
Catalog No. T5S0331Alias NeoisoliquritinCas No. 5041-81-6
1. Isoliquiritin (Neoisoliquritin) has antitussive effects. 2. Isoliquiritin has antidepressant-like effects. 3. Isoliquiritin, liquiritin and isoliquirigenin inhibits the p53-dependent pathway and shows crosstalk between Akt activities.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$39In StockIn Stock
5 mg$72In StockIn Stock
10 mg$123In StockIn Stock
25 mg$249In StockIn Stock
50 mg$373-In Stock
100 mg$549-In Stock
500 mg$1,170-In Stock
1 mL x 10 mM (in DMSO)$67In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.88%
Appearance:Solid
Color:White to Yellow
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Product Introduction

Isoliquiritin AI Summary
Isoliquiritin demonstrates multifaceted inhibitory bioactivity. Specifically, it functions as an inhibitor of the Spanish flu (A/Bervig_Mission/1/18) neuraminidase, with an IC50 value of 124,000 nM in one assay and a Ki value of 94,000 nM in a noncompetitive inhibition assay. Furthermore, it effectively inhibits human recombinant aldose reductase, exhibiting an IC50 of 720 nM. Additionally, Isoliquiritin inhibits the PTP1B enzyme (source unspecified) using p-nitrophenyl phosphate as a substrate at a concentration of 100 µM, with observed inhibition of less than 50%. Lastly, it inhibits the human DPP4 enzyme with an IC50 value of 26,920 nM, as determined using the H-Gly-Pro-AMC peptide substrate in a fluorimetric assay..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. Isoliquiritin (Neoisoliquritin) has antitussive effects. 2. Isoliquiritin has antidepressant-like effects. 3. Isoliquiritin, liquiritin and isoliquirigenin inhibits the p53-dependent pathway and shows crosstalk between Akt activities.
SynonymsNeoisoliquritin
Chemical Properties
Molecular Weight418.39
FormulaC21H22O9
Cas No.5041-81-6
SmilesOC[C@H]1O[C@@H](Oc2ccc(\C=C\C(=O)c3ccc(O)cc3O)cc2)[C@H](O)[C@@H](O)[C@@H]1O
Relative Density.1.528g/cm3
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 237.5 mg/mL (567.65 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.78 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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Dose Conversion

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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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