Description |
Kushenol K, a flavonoid antioxidant isolated from the roots of Sophora flavescens. Kushenol K is a cytochrome P-450 3A4 (CYP3A4) inhibitor with a Ki value of 1.35 μM[1]. Kushenol K shows weak antiviral activity against HSV-2 (EC50 of 147 μM)[2]. Kushenol K also inhibits the activity of SGLT1 and SGLT2[3].
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Target |
HSV-2:147 μM (EC50)
CYP3A4:1.35 μM (Ki)
SGLT
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In Vitro |
When Midazolam is used as the substrate of CYP3A4, Kushenol K exhibits the strong inhibition with an IC50 values of 1.62 µM[1]. At a concentration of 50 μM, the inhibition rate of Kushenol K on SGLT1 is 29.7%, and the inhibition rate on SGLT2 is 43.7%[3].
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Density | 1.3±0.1 g/cm3 |
Boiling Point | 722.4±60.0 °C at 760 mmHg |
Flash Point | 242.4±26.4 °C |
Exact Mass | 472.209717 |
LogP | 3.81 |
Vapour Pressure | 0.0±2.5 mmHg at 25°C |