Gypenoside XVII, a novel phytoestrogen belonging to the gypenosides, can activate estrogen receptors.

Solid

Estrogen receptor

The ability of Gypenoside XVII (GP-17) to prevent Ox-LDL-induced cytotoxicity is detected by cell viability assays. Gypenoside XVII does not demonstrate any cytotoxicity in HUVECs.Gypenoside XVII can protect HUVECs against Ox-LDL-induced apoptosis.Gypenoside XVII dose-dependently mitigates the toxic effect of Ox-LDL on HUVEC viability.The viability of HUVECs is significantly higher than that of other groups at 50 μg/mL Gypenoside XVII .Medlife has not independently confirmed the accuracy of these methods. They are for reference only.

Body weights are measured as physical measures of hormone bioactivity. Mean body weights are significantly higher in every group compared to that of the control, but there is no significant difference in body weight between the different treatments during the 10-week feeding. The mouse plasma lipid levels are also measured at the end of 10 weeks of a high-fat diet. Circulating levels of total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-C) are significantly increased in the treated groups of ApoE mice compared with those of the C57BL/6J control group; Gypenoside XVII (GP-17) and Probucol treatment substantially decreases both of these parameters relative to those of the ApoE model group.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.

Room temperature or refrigerated transport.

4°C, Keep In Dark；*In solvent : -80°C, 6 months; -20°C, 1 month (Keep In Dark)；

Terpenoids
Triter

Plants

体外研究:
DMSO : ≥ 100 mg/mL(105.58 mM)
H₂O : 41.67 mg/mL(44.00 mM;Need ultrasonic)
*≥ means soluble, but saturation unknown.