Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

4'-Hydroxywogonin

Copy Product Info
😃Good
Catalog No. TN1276Cas No. 57096-02-3
Alias 8-Methoxyapigenin

4'-Hydroxywogonin (8-Methoxyapigenin), a natural flavonoid with anti-inflammatory properties, reduced the production of pro-inflammatory cytokines (e.g., TNF-α, IL-6, and IL-1β), inhibited the TAK1/IKK/NF-κB signaling pathway, and reduced the phosphorylation of MAPKs and the PI3/Akt signaling pathway.

4'-Hydroxywogonin

4'-Hydroxywogonin

Copy Product Info
😃Good
Catalog No. TN1276Alias 8-MethoxyapigeninCas No. 57096-02-3
4'-Hydroxywogonin (8-Methoxyapigenin), a natural flavonoid with anti-inflammatory properties, reduced the production of pro-inflammatory cytokines (e.g., TNF-α, IL-6, and IL-1β), inhibited the TAK1/IKK/NF-κB signaling pathway, and reduced the phosphorylation of MAPKs and the PI3/Akt signaling pathway.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$1,9807-10 days7-10 days
Add to Cart
Add to Quotation
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.
Questions
TargetMol
View More

Batch Information

Select Batch
Appearance:Solid
Color:Yellow
Contact us for more batch information

Resource Download

Product Introduction

Bioactivity
Description
4'-Hydroxywogonin (8-Methoxyapigenin), a natural flavonoid with anti-inflammatory properties, reduced the production of pro-inflammatory cytokines (e.g., TNF-α, IL-6, and IL-1β), inhibited the TAK1/IKK/NF-κB signaling pathway, and reduced the phosphorylation of MAPKs and the PI3/Akt signaling pathway.
In vitro
4'-Hydroxywogonin suppressed the expression of COX-2 and iNOS in LPS-stimulated RAW 264.7 macrophages after 24-hour incubation with 0.5–15 μM concentrations, as demonstrated by Western blot analysis. [1]
Treatment with 0.5–15 μM 4'-Hydroxywogonin for 24 hours reduced the production of nitric oxide (NO) and prostaglandin E2 (PGE2) in RAW 264.7 cells, as measured by Griess assay and ELISA, respectively. [1]
4'-Hydroxywogonin downregulated the expression of pro-inflammatory cytokines (TNF-α, IL-6, IL-1β) at the mRNA level after 4 hours (qRT-PCR) and at the protein level after 24 hours (Western blot) in RAW 264.7 macrophages. [1]
Pre-treatment with 0.5–15 μM 4'-Hydroxywogonin for 1 hour inhibited the LPS-induced interaction between TAK1 and TAB1 and suppressed downstream activation of the TAK1/IKK/NF-κB pathway, as shown by co-immunoprecipitation and Western blot performed 30–60 minutes post-stimulation. [1]
4'-Hydroxywogonin reduced phosphorylation of ERK, JNK, p38 MAPKs, and Akt in RAW 264.7 cells after 30 minutes of LPS stimulation, confirmed by Western blot following pre-treatment with 0.5–15 μM. [1]
4'-Hydroxywogonin significantly decreased intracellular reactive oxygen species (ROS) levels in LPS-stimulated RAW 264.7 cells, as detected by DCFH-DA fluorescence staining after 30–60 minutes of incubation. [1]
In vivo
In an LPS-induced acute lung injury (ALI) mouse model, intraperitoneal injection of 4'-Hydroxywogonin at doses of 2.5, 5, or 10 mg/kg significantly suppressed the expression of COX-2 and iNOS in lung tissues, as shown by Western blot and immunohistochemistry. [1]
Treatment with 4'-Hydroxywogonin markedly reduced nitric oxide (NO) and prostaglandin E2 (PGE2) levels in bronchoalveolar lavage fluid (BALF), measured by Griess assay and ELISA. [1]
The levels of pro-inflammatory cytokines TNF-α and IL-6 in BALF decreased after 4'-Hydroxywogonin administration, indicating a systemic anti-inflammatory effect. [1]
4'-Hydroxywogonin alleviated lung tissue damage by reducing inflammatory cell infiltration and preserving alveolar structure. [1]
4'-Hydroxywogonin decreased the lung wet-to-dry weight ratio, suggesting a protective effect against LPS-induced pulmonary edema. [1]
Synonyms8-Methoxyapigenin
Chemical Properties
Molecular Weight300.26
FormulaC16H12O6
Cas No.57096-02-3
SmilesO=C1C=C(OC=2C(OC)=C(O)C=C(O)C12)C=3C=CC(O)=CC3
Relative Density.1.512 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.

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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

Keywords

Related Tags: buy 4'-Hydroxywogonin | purchase 4'-Hydroxywogonin | 4'-Hydroxywogonin cost | order 4'-Hydroxywogonin | 4'-Hydroxywogonin chemical structure | 4'-Hydroxywogonin in vivo | 4'-Hydroxywogonin in vitro | 4'-Hydroxywogonin formula | 4'-Hydroxywogonin molecular weight