G-protein-coupled receptor regulators and methods of use thereof
US-2024417378-A1 · Dec 19, 2024 · US
US2025059203A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025059203-A1 |
| Application number | US-202218723290-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 21, 2022 |
| Priority date | Dec 21, 2021 |
| Publication date | Feb 20, 2025 |
| Grant date | — |
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The present invention relates to an anticancer use of aristoloxazine C, and more specifically to a pharmaceutical composition and a health functional food composition which use aristoloxazine C represented by Chemical Formula 1 or an isomer or pharmaceutically acceptable salt thereof, a method for preventing, ameliorating or treating cancer by using same; and a method for isolating aristoloxazine C.
Opening claim text (preview).
1 - 8 . (canceled) 9 . A method for isolating aristoloxazine C represented by Chemical Formula 1 from Asarum heterotropoides roots, comprising the steps of: (a) extracting Asarum heterotropoides roots with an ethanol solvent to obtain an ethanol extract of the Asarum heterotropoides roots; (b) obtaining an ethyl acetate fraction by systematically fractionating the ethanol extract of the Asarum heterotropoides roots in the order of hexane, ethyl acetate and water; (c) performing flash chromatography on the ethyl acetate fraction by using a water-methanol mixture as an effluent solvent to obtain a fraction; and (d) purifying the aristoloxazine C by subjecting the fraction obtained after performing column chromatography to semi-preparative chromatography by using a water-acetonitrile mixture as an effluent solvent. 10 . The method of claim 9 , wherein the ethanol solvent in step (a) is 50 to 90% ethanol. 11 . The method of claim 9 , wherein the water-methanol mixture in step (c) is applied at a concentration gradient of 6:4 to 1:9. 12 . The method of claim 9 , wherein the water-acetonitrile mixture in step (d) is applied at a concentration gradient of 6.5:3.5 to 5.5:4.5. 13 . A method for preventing, ameliorating or treating cancer, comprising the step of administering aristoloxazine C represented by Chemical Formula 1, an isomer or a pharmaceutically acceptable salt thereof to a subject in need thereof: 14 . The method of claim 13 , wherein the isomer includes a racemate, an enantiomer, a diastereomer, a mixture of enantiomers or a mixture of diastereomers. 15 . The method of claim 13 , wherein the aristoloxazine C is isolated from Asarum heterotropoides roots. 16 . The method of claim 13 , wherein the aristoloxazine C, isomer or pharmaceutically acceptable salt thereof exhibits an effect of inhibiting cancer cells or inhibiting or delaying tumor development. 17 - 20 . (canceled)
Complex extraction schemes, e.g. fractionation or repeated extraction steps · CPC title
using mixed solvents, e.g. 70% EtOH · CPC title
Preparations for use in therapy · CPC title
Asarum (wild ginger) · CPC title
ortho- or peri-condensed with carbocyclic ring systems · CPC title
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