MDL | MFCD00017736 |
---|---|
Molecular Weight | 284.26 |
Molecular Formula | C16H12O5 |
SMILES | O=C1C=C(C2=CC=CC=C2)OC3=C(OC)C(O)=CC(O)=C13 |
CDK8 |
Wogonin (0-200 μM) exhibits a dose- and time- dependent reduces in cell viability of caco-2, SW1116 and HCT116 cells. Wogonin (10-40 μM) induces G1 phase arrest in HCT-116 cells. Wogonin also supresses Wnt signaling pathway in HCT116 cells. Wogonin interfers in the activity of transcription factor TCF/Lef family. Moreover, Wogonin inhibits β-catenin-mediated transcription through suppressing the activity of CDK8 [1] . Wogonin shows cytotoxic and antiproliferative effects on HeLa cells. Wogonin (90 µM) induces cell cycle arrest at G0-G1 phase, and suppresses the levels of cyclin D1 and Cdk4 markedly in HeLa cells [2] . Wogonin (1.25, 2.5, 5, 10, 20 μg/ml) suppresses EtOH-induced inflammatory response in RAW264.7 cells [3] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Wogonin (30, 60 mg/kg) reduces tumor growth of HCT116 cells in a xenograft model [1] . Wogonin (25, 50, 100 mg/kg) protects against liver injury and pathological characteristics of ALD in mice. Wogonin activates PPAR-γ expression in mice with ALD and EtOH induced RAW264.7 cells [3] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
DMSO : 62.5 mg/mL ( 219.87 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.5179 mL | 17.5895 mL | 35.1791 mL |
5 mM | 0.7036 mL | 3.5179 mL | 7.0358 mL |
10 mM | 0.3518 mL | 1.7590 mL | 3.5179 mL |
Add each solvent one by one: 0.5% CMC-Na /saline water
Solubility: 24 mg/mL (84.43 mM); Suspended solution; Need ultrasonic