Polyhydroxy long-chain fatty acid, separation and extraction method thereof and application thereof in inhibiting the activity of aromatizing enzyme
A long-chain fatty acid, polyhydroxyl technology, applied in the separation/purification of carboxylic acid compounds, organic active ingredients, medical preparations containing active ingredients, etc., to achieve the effect of strong aromatase inhibitory activity
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Embodiment 110
[0039] Embodiment 110,11, the preparation of 12-trihydroxy heptadecadienoic acid
[0040] 1) Supercritical extraction: commercially available rape pollen (produced by Baikang Bee Industry, Xuancheng City, Anhui Province) was dried under reduced pressure at 60°C for 24 hours, and then the dried pollen was dried at 40°C and the pressure of the extraction kettle was 40MPa. Separation kettle I temperature 35 ℃, pressure 12MPa, separation kettle II temperature 25 ℃, pressure 5MPa, the weight concentration of pollen weight 8% is 95v / v% ethanol as entrainer to carry out supercritical carbon dioxide (45L / hour circulation consumption) extraction After 2.0 hours, the supercritical extraction fraction was obtained, and the supercritical extract was collected.
[0041] 2) Macroporous resin enrichment: steam the extract obtained in step 1 until it has no alcohol smell, and mix the sample in a way similar to the traditional silica gel column dry method, that is, take 20-60% of the column v...
Embodiment 210
[0044] Embodiment 210,11, the preparation of 12-trihydroxy heptadecadienoic acid
[0045] 1) Extraction: take rapeseed pollen after breaking the wall, pulverize, add 10ml / g rapeseed pollen, heat reflux or cold soak and percolate 3 times with 95% ethanol by volume, filter, combine filtrates, recover solvent under reduced pressure, and obtain relative Fluid extract with a density of 1.28. Distributed in water, extracted successively with petroleum ether, chloroform and ethyl acetate, the amount of each extraction solvent is equal to the volume of aqueous solution, and each solvent is extracted several times until it is almost colorless. The ethyl acetate extraction part was taken, the solvent was recovered under reduced pressure, and the effective part was obtained by evaporating to dryness.
[0046] 2) Column chromatography: Mix the above-mentioned effective parts with silica gel on the column, perform silica gel (300-400 mesh) column chromatography (silica gel with ten times ...
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