| Name | sophoraflavanone G |
|---|---|
| Synonyms |
4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-methyl-2-(1-methylethenyl)-4-hexen-1-yl]-, (2S)-
Sophoraflavanone G (2S)-2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-isopropenyl-5-methyl-4-hexen-1-yl]-2,3-dihydro-4H-chromen-4-one Kushenol F Norkurarinone Vexibinol Nor-kurarinone |
| Description | Sophoraflavanone G (Kushenol F) is iaolated from Sophora flavescens and shows anti-tumor and anti-inflammatory properties. Sophoraflavanone G (Kushenol F) induces MDA-MB-231 and HL-60 cells apoptosis through suppression of MAPK-related pathways[1][2]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 29.7 μM (MDA-MB-231 cell)[1] |
| In Vitro | Sophoraflavanone G (0 -100 μM; 24 hours) decreases the viability of the HL-60 cells in a dose-dependent manner[1]. Sophoraflavanone G (0 -100 μM; 24 hours) induces HL-60 cell apoptosis, activated caspase-3 and caspase-9, and downregulated Bcl-2 and Bcl-xL. It also upregulates Bax and released cytochrome c from the mitochondria into the cytoplasm, enabling apoptosis via the mitochondrially-mediated "intrinsic" pathway[1] Sophoraflavanone G (0 -40 μM; 24 hours) inhibits MDA-MB-231 cell viability in a concentration-dependent manner, with an IC50 value of 29.7 ± 5.2 μM[2]<.br> |
| References |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 659.3±55.0 °C at 760 mmHg |
| Melting Point | 173-175℃ |
| Molecular Formula | C25H28O6 |
| Molecular Weight | 424.486 |
| Flash Point | 224.8±25.0 °C |
| Exact Mass | 424.188599 |
| PSA | 107.22000 |
| LogP | 6.52 |
| Vapour Pressure | 0.0±2.1 mmHg at 25°C |
| Index of Refraction | 1.623 |
| Storage condition | 2-8℃ |
| Hazard Codes | Xi |
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