8-(C-beta-D-glycopyranyl)-7,3',4'-trihydroxyflavone, its separating process, medical composition and used for medicine for diabets
A technology of trihydroxyflavone and pyranyl, which is applied in the field of separating the new compound 8--7 and treating diabetes, and can solve the problem of not providing detailed information on biological activity and not publicly preparing the water extract of the heartwood of Indian jina tree methods, methods for isolating chemical components are not disclosed, etc.
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Embodiment 1
[0045] Using 80% hydrated ethanol (3×3 liters), the powdery heartwood of the Indian Gina tree was percolated for 48 hours. The obtained concentrate was partitioned sequentially with hexane, chloroform, propanol and butanol. The polar extract was subjected to MPLC treatment using silica gel (100-200 mesh) to obtain a total fraction of sequentially using hexane, chloroform, methanol, and ethanol. The active compound is obtained by using CHCl 3 Purification by repeated MPLC and flash chromatography on silica gel (230-400 mesh) with MeOH (19:1) as solvent afforded 8-(C-β-D-glucopyranyl)-7,3' , 4'-trihydroxyflavone, the yield is 0.046%, mp.202-204℃, [α] D 19 +25.6° (MeOH, c, 0.5).
Embodiment 2
[0047] Using hot water, the heartwood of the Indian Gina tree was extracted for 4×4 hours. The obtained concentrate was partitioned successively between hexane, chloroform, propanol and butanol. The obtained polar extract was subjected to flash chromatography, using hexane, chloroform, ethyl acetate and methanol as solvent system, using silica gel (100-200 mesh) to obtain 8-(C-β- Fraction of D-glucopyranyl)-7,3',4'-trihydroxyflavone, which was then chromatographed repeatedly on silica gel (230-400 mesh) using EtOAc-MeOH (19.5:0.5) as solvent, 8-(C-β-D-glucopyranyl)-7,3',4'-trihydroxyflavone of structural formula 1 was obtained with a yield of 0.049%, mp.202-204°C, [α] D 19 +25.6° (MeOH, c, 0.5).
Embodiment 3
[0049] The heartwood of the Indian Jina tree was boiled (16 times) with water until 1 / 4 volume of water remained. Filtered, concentrated and partitioned sequentially between hexanes, chloroform, propanol and n-butanol. The resulting polar extract was subjected to column chromatography using hexane, chloroform, ethyl acetate and methanol as the solvent system, using silica gel (60-120 mesh) to obtain a compound rich in 8-(C-β-D -Glucopyranyl)-7,3',4'-trihydroxyflavone fractions. The fraction rich in 8-(C-β-D-glucopyranyl)-7,3',4'-trihydroxyflavone was continued to use the mixture of ethyl acetate-acetone (8:2) in Repeat column chromatography on silica gel (100-200 mesh) to obtain 8-(C-β-D-glucopyranyl)-7,3',4'-trihydroxyflavone with a yield of 0.051%, mp. 202-204°C, [α] D 19 +25.6° (MeOH, c, 0.5).
[0050] advantage:
[0051] 1. The obtained compound 8-(C-β-D-glucopyranyl)-7,3',4'-trihydroxyflavone is a new molecule with antidiabetic activity.
[0052]2. The method for s...
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