Composition of active ingredients of alisma rhizome, and medical application
A technology of active ingredient and composition, applied in the field of active ingredient composition of Alisma, can solve problems such as complex chemical composition
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Embodiment 1
[0034] Preparation of herbal extract:
[0035] Method a: Take 2 kg of dry tubers of Alisma orientalis (Sam.) Juzep., a plant of the family Alismaceae, crush them, and extract twice with 4 liters of chloroform under reflux, each time for 3 hours. The extracts were combined, and the solvent was recovered to obtain 87 grams of oily extract.
[0036] Method b: take 2 kg of dried tubers of Alisma orientalis (Sam.) Juzep., and grind them, percolate with 80% ethanol, recover ethanol, and obtain 94 grams of oil.
[0037] Method c: Take the dry tuber of Alisma orientalis (Sam.) Juzep., which is a plant of the family Alismaceae, and crush it, pass through a 20-mesh sieve, weigh 4 kg of the medicinal powder, and put it in a 10L extraction barrel for supercritical carbon dioxide extraction. Extraction conditions: the pressure of carbon dioxide is 20-45MPa, extraction temperature 46-49°C, extraction time 2.5 hours, to obtain 150g of oil.
[0038] Method d: Take 1 kg of dried tuber pieces...
Embodiment 2
[0041] Preparation of alisitol B23-acetate:
[0042]Method a: Weigh 100 grams of the oily extract of Example 1, put it on a silica gel column (500 grams) and elute it with petroleum ether and ethyl acetate (10:1), then wash it with petroleum ether and ethyl acetate (10:3) Elution, 200mL as a fraction, detected by TLC, collected the target fraction, and obtained 0.8g of crystals. Recrystallization from petroleum ether-ethyl acetate gave 0.5 g of crystals. Identified as alisol B23-acetate.
[0043] Method b: Weigh 100 grams of the oily extract of Example 1, put it on an aluminum oxide (500 grams) column and wash it with petroleum ether and chloroform (20:1), and then wash it with petroleum ether and chloroform (10:1). 200mL was taken as a fraction, detected by TLC, and the target fraction was collected to obtain 0.7g of crystals. After recrystallization from methanol, 0.5 g of crystals were obtained, which were identified as alisitol B23-acetate.
Embodiment 3
[0045] Preparation of Alisitol A24-acetate:
[0046] Method a: According to the method a of Example 2, after the petroleum ether and ethyl acetate (10:3) are eluted, then eluted with petroleum ether and ethyl acetate (10:5), detected by TLC, and the target is collected Fractions obtained 0.4 g of crystals, and recrystallized from petroleum ether-ethyl acetate to obtain 0.3 g. Identified as alisol A24-acetate.
[0047] Method b: According to the method b of Example 2, after the petroleum ether and chloroform (10:1) were eluted, then petroleum ether and chloroform (10:3) were eluted, and TLC was used to detect, collect the target fraction, and obtain crystallization 0.4 g, and 0.3 g of crystals were obtained after recrystallization from methanol. Identified as alisol A24-acetate.
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