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Luteolin (Standard)

(Synonyms: Luteolol (Standard), Luteoline (Standard), Digitoflavone (Standard)) Copy Product Info
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Synonyms: Luteolol (Standard), Luteoline (Standard), Digitoflavone (Standard)

Catalog No. TMSM-2565 Copy Product Info
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Luteolin (Standard) is a reference compound for analytical and biochemical research involving Luteolin. Luteolin (Standard) belongs to the flavonoid class and functions as a Nrf2 inhibitor and PDE inhibitor. Luteolin (Standard) is utilized in biomedical research focused on flavonoid signaling modulation, oxidative stress regulation, inflammatory pathway analysis, and enzyme inhibition profiling across tumor, infectious, and allergic disease models.
Luteolin (Standard)
Cas No. 491-70-3
Pack SizePriceUSA StockGlobal StockQuantity
25 mg$487-10 days7-10 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Luteolin (Standard) is a reference compound for analytical and biochemical research involving Luteolin. Luteolin (Standard) belongs to the flavonoid class and functions as a Nrf2 inhibitor and PDE inhibitor. Luteolin (Standard) is utilized in biomedical research focused on flavonoid signaling modulation, oxidative stress regulation, inflammatory pathway analysis, and enzyme inhibition profiling across tumor, infectious, and allergic disease models.
In vitro
Methods
Human lung cancer NCI-H460 cells were treated with luteolin at various concentrations for different durations. Cell viability, cell cycle, apoptosis and the expression of related proteins were detected.
Results
1.Luteolin at 0–160 μM inhibited the viability of NCI-H460 cells in a concentration-dependent manner after 24-hour treatment .
2.Treatment with 20–80 μM luteolin for 24 hours induced S-phase cell cycle arrest .
3.Luteolin at 320–580 μM induced cell apoptosis following 48-hour incubation .
4.After 24-hour treatment with 20–80 μM luteolin, the Bax/Bcl-2 ratio was upregulated in a concentration-dependent manner. Only 80 μM luteolin downregulated Bad expression, and Sirt1 protein levels were decreased dose-dependently within this concentration range [1].
In vivo
Methods:Male Wistar rats with non-alcoholic steatohepatitis induced by high-fat and high-sugar diet were intragastrically administered luteolin at doses of 10–100 mg/kg daily for 12 consecutive weeks. The antioxidant capacity and changes of inflammation-related pathways were evaluated.
Results:Luteolin exhibited antioxidant activity. It targeted and inhibited the pro-inflammatory pathways of IL-1 and IL-18, thereby effectively preventing non-alcoholic steatohepatitis in rats [2].
SynonymsLuteolol (Standard), Luteoline (Standard), Digitoflavone (Standard)
Chemical Properties
Molecular Weight286.24
FormulaC15H10O6
Cas No.491-70-3
SmilesO=C1C=C(OC=2C=C(O)C=C(O)C12)C=3C=CC(O)=C(O)C3
Relative Density.1.2981 g/cm3 (Estimated)
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: 80 mg/mL (279.49 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.4936 mL17.4679 mL34.9357 mL174.6786 mL
5 mM0.6987 mL3.4936 mL6.9871 mL34.9357 mL
10 mM0.3494 mL1.7468 mL3.4936 mL17.4679 mL
20 mM0.1747 mL0.8734 mL1.7468 mL8.7339 mL
50 mM0.0699 mL0.3494 mL0.6987 mL3.4936 mL
100 mM0.0349 mL0.1747 mL0.3494 mL1.7468 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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% Saline/PBS/ddH2O

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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
Related Tags: Luteolin (Standard) chemical structure | Luteolin (Standard) in vivo | Luteolin (Standard) in vitro | Luteolin (Standard) formula | Luteolin (Standard) molecular weight