Novel flavane derivative and its preparation method and uses
A kind of derivative, flavan technology, applied in the new flavan derivative and its preparation and use field
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Embodiment 1
[0083] Operate according to the process flow diagram shown in accompanying drawing 1, 70g dried monkey earring leaves are crushed in a blender, extracted twice with 350ml of 95% ethanol solution under reflux, filtered, and the combined filtrate is concentrated to a specific gravity of about 1.05 (65°C) Crude extract 200ml. Separation on a macroporous resin column according to the conventional method, after the crude extract passes through the column, it is eluted with a gradient of 0-95% water-alcohol solution, the eluate of 40-95% ethanol is collected, the solvent is recovered, concentrated in vacuo, and dried to obtain The dry product of effective part A is 8.2 g, and the content of cyperol is determined to be 32% by the above-mentioned colorimetric method.
Embodiment 2
[0085] With the method of Example 1, operate according to the process flow diagram shown in accompanying drawing 1, take 70g dried monkey earring leaves, extract with 95% ethanol solution, separate on the macroporous resin column on the crude extract, 0-95% water- Gradient elution with alcohol solution, collecting the eluate of 40-65% ethanol, recovering the solvent, concentrating in vacuo and drying to obtain 5.3 g of active site I. Using the above-mentioned thin-layer scanning method, the content of saicinol I was determined to be 11.7%; the eluate of 65-95% ethanol was collected, the solvent was recovered, concentrated in vacuo, and dried to obtain 1.5 g of active site II. Using the above-mentioned thin-layer scanning method, the content of cylinol II was determined to be 17.7%.
[0086] Take 0.7g of active site I, separate it on a silica gel column (30g), and use chloroform:methanol:formic acid for elution in a solvent system with a volume ratio of 6:1:0.5. Evaporate to d...
Embodiment 3
[0091]Operate according to the process flow diagram shown in accompanying drawing 1, get 200g monkey earring dried leaves and add water 1800ml to decoct and extract twice at a time, medicinal liquid ultrafiltration, merging and concentrating get specific gravity about 1.05 (65 °) and take crude extract 2020ml , separated on a polyamide column according to a conventional method, and after the crude extract passed through the column, it was eluted with a gradient of 0-95% water-alcohol solution, and the eluate of 40-95% ethanol was collected, the solvent was recovered, concentrated in vacuo, and dried. 21 g of the crude product of active site A was obtained. Refined with acetone-water solvent system to obtain 15 g of refined product of active part. The content of the monkey earring phenol was 32.5% by colorimetric method.
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