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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 Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | $1,980 | 7-10 days | 7-10 days |
| 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] |
| Synonyms | 8-Methoxyapigenin |
| Molecular Weight | 300.26 |
| Formula | C16H12O6 |
| Cas No. | 57096-02-3 |
| Smiles | O=C1C=C(OC=2C(OC)=C(O)C=C(O)C12)C=3C=CC(O)=CC3 |
| Relative Density. | 1.512 g/cm3 (Predicted) |
| Storage | keep 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. |
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.
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.
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