Application of long-chain fatty acid derivative or plant extracts containing same in inhibiting the activity of aromatizing enzyme
A technology for aromatase activity and long-chain fatty acids, which is applied in the application field of a class of long-chain fatty acid derivatives or plant extracts containing them in inhibiting aromatase activity, so as to inhibit aromatase activity and prevent and treat benign prostatic hyperplasia effect of disease
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Embodiment 1
[0031] The preparation of embodiment 1N-(2-hydroxyethyl) linolenamide, dihydroxy octadecadienoic acid, linolenic acid fructoside and palmitic acid sorbitol ester
[0032] 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.
[0033] 2) Macroporous resin enrichment: use macroporous resin column chromatography (DA201 resin with 10 times the sample mass, Tianjin Huida Chemic...
Embodiment 2
[0037] The preparation of embodiment 2N-(2-hydroxyethyl) linolenamide, 1-linolenic acid glyceride, dihydroxy octadecadienoic acid, linolenic acid fructoside and palmitic acid sorbitol ester
[0038] 1) Extraction: take rapeseed pollen after breaking the wall, pulverize, heat and reflux 3 times with 95% ethanol aqueous solution with a volume concentration of 10ml / g rapeseed pollen, filter, combine the filtrates, and recover the solvent under reduced pressure to obtain a relative density of 1.28 The liquid extract is dissolved in water at the ratio of 2ml water / g liquid extract, and is extracted successively with sherwood oil, chloroform and ethyl acetate. colorless. Take the ethyl acetate extraction part, recover the solvent under reduced pressure, and evaporate to dryness to obtain the effective part.
[0039] 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 10 ...
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