A kind of method that prepares 20-glucose-ginsenoside rf monomer from pearl ginseng
A technology of ginsenosides and bead ginseng, which is applied in the field of natural medicinal chemistry, can solve the problems of cumbersome process, many organic solvents, low yield and the like, and achieves the effect of simple process and reduced dosage.
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Embodiment 1
[0019] Pearl ginseng 10 kg, 70% ethanol water reflux extraction 3 times, the amount of ethanol was 10, 8, 8 times (V / V) respectively, the reflux time was 1.5h, 1.0h, 1.0h respectively, the three extractions were combined, and the solvent was recovered , After drying, 1400 g of the extract of ginseng was obtained.
[0020] Get 50 g of Ginseng extract, separate it with silica gel column chromatography, the mobile phase is dichloromethane: methanol: water (6:1:0.5, volume ratio), to obtain 10 g of component B containing 20-glucose-ginsenoside Rf; Component B is separated by ODS column chromatography, and the mobile phase is methanol-water (1:2, volume ratio) to obtain 8g of component I containing 20-glucose-ginsenoside Rf; component I is separated by high-speed countercurrent chromatography ( HSCCC) was separated, and the solvent ratio was n-butanol-ethyl acetate-water (4:1:5, volume ratio) as the solvent system for preparative countercurrent chromatography separation, and the fl...
Embodiment 2
[0033] Get the total extract 50g of Radix Ginseng, separate with silica gel column chromatography, mobile phase is ethyl acetate: methanol: water (7:1:0.5, volume ratio), obtain the component B9 that contains 20-glucose-ginsenoside Rf. 1g; Component B is separated by ODS column chromatography, and the mobile phase is methanol-water (1:1.5, volume ratio), to obtain 7.3g of component I containing 20-glucose-ginsenoside Rf; Countercurrent chromatography (HSCCC) was used for separation, and the solvent ratio was n-butanol-ethyl acetate-water (4:1:5, volume ratio) as the solvent system for preparative countercurrent chromatography separation, and the flow rate was 2mL min -1 , the speed is 800r·min -1 , the detection wavelength is 203nm.
[0034] The specific operation is as follows: take 1200mL of n-butanol, 300mL of ethyl acetate, and 1500mL of water, put them in a 2000mL separatory funnel, oscillate and shake well, and let stand overnight. The upper phase is the stationary pha...
Embodiment 3
[0038] Get the total extract 50g of Radix Ginseng, separate with silica gel column chromatography, mobile phase is ethyl acetate: ethanol: water (7:1:1, volume ratio), obtain the component B8 that contains 20-glucose-ginsenoside Rf. 5g; Component B is separated by ODS column chromatography, and the mobile phase is methanol-water (1:1.5, volume ratio), to obtain 6.9g of component I containing 20-glucose-ginsenoside Rf; Countercurrent chromatography (HSCCC) was used for separation, and the solvent ratio was n-butanol-ethyl acetate-water (4:1:5, volume ratio) as the solvent system for preparative countercurrent chromatography separation, and the flow rate was 2mL min -1 , the speed is 800r·min -1 , the detection wavelength is 203nm.
[0039] The specific operation is as follows: take 1200mL of n-butanol, 300mL of ethyl acetate, and 1500mL of water, put them in a 2000mL separatory funnel, oscillate and shake well, and let stand overnight. The upper phase is the stationary phase,...
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