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Synonyms:
Anhydrohirundigenin mono-thevetoside
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Anhydrohirundigenin mono-thevetoside is an apoptosis inducer. It increases the expression levels of caspase-3, caspase-9, and Bax, while decreasing the expression level of Bcl-2. This compound induces cell cycle arrest at the G1 phase and is applicable in research related to liver cancer, lung cancer, and breast cancer. |
| In vitro | Anhydrohirundigenin mono-thevetoside (Compound 4) effectively inhibits the viability of A549, HepG2, and 4T1 cells in vitro within a concentration range of 0.1-100 μM for 48 hours, showing the strongest activity against HepG2 cells (IC₅₀ = 12.24 μM). At concentrations of 1-20 μM over 48 hours, it induces dose-dependent G1 phase arrest and apoptosis in HepG2 cells. Additionally, this compound upregulates the expression of caspase-3, caspase-9, and Bax, while downregulating caspase-8 and Bcl-2 in a dose-dependent manner. |
| Molecular Weight | 504.61 |
| Formula | C28H40O8 |
| Cas No. | 849201-83-8 |
| Smiles | C[C@@]12[C@@]3([C@@]4(C(=C5[C@](CC4)([C@]6(C)C(=CC5)C[C@@H](O[C@H]7[C@H](O)[C@@H](OC)[C@H](O)[C@@H](C)O7)CC6)[H])O[C@@]3(CO1)[H])CO2)[H] |
| Storage | 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.
| Size | Quantity | Unit Price | Amount | Operation |
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