Medicinal composition containing resveratrol and being capable of inhibiting drug-resisting staphylococcus aureus
A technology of resveratrol and Staphylococcus aureus, which is applied in the field of pharmacy, can solve the problem that the antibacterial effect of resveratrol has not been seen yet, and achieve the effect of improving sensitivity
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Embodiment 1
[0033] Embodiment 1 prepares compound Resveratrol
[0034] Take 202.6 g of dried roots of Sophora davidii, crush them, soak them in 95% ethanol (3 L x 3 times), combine the extracts and evaporate to dryness under reduced pressure to obtain 18.5 g of extract. The extract was sequentially extracted with petroleum ether, chloroform, and methanol, wherein 13.9 g of the methanol part was obtained, and the methanol part was separated by silica gel column chromatography, and the eluent was dichloromethane-methanol (100:0-0:100), gradient washing After removal, silica gel thin-layer chromatography detection, the fractions were collected to obtain 570.4 mg of mixture 9, and mixture 9 obtained 27.2 mg of colorless needle crystals through repeated column chromatography on gel and silica gel, which was detected as a pure compound by silica gel thin-layer chromatography and HPLC. Identified as Resveratrol by spectral data.
Embodiment 2
[0035] Embodiment 2 prepares compound Resveratrol
[0036] Utilize high-speed countercurrent chromatography (TBE-300 type high-speed countercurrent chromatography) to separate and purify resveratrol in Polygonum cuspidatum (Polygonumcuspidatum), select the solvent system as: chloroform: methanol: water = 4: 3: 2, rotating speed 850r / min, flow rate 2ml / min, and the ultraviolet detection wavelength is 280nm; under this condition, the yield of resveratrol is 0.186%, and the purity is greater than 96%.
Embodiment 3
[0037] Embodiment 3 prepares compound Resveratrol
[0038] With 3,5-dimethoxybenzaldehyde (1) as starting material, obtain 3 through demethylation reaction under the effect of anhydrous aluminum trichloride, 5-dihydroxybenzaldehyde (2), then with p- Hydroxyphenylacetic acid undergoes Perkin condensation under the action of acetic anhydride and triethylamine to obtain (E)-2-(4'-hydroxyphenyl)-3-(3',5'-dihydroxyphenyl)acrylic acid (4) , and finally the target compound resveratrol (5) was obtained through synchronous decarboxylation-isomerization reaction with a total yield of 41.9%.
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