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Novel Lepidium meyenii Walp. alkaloid, and preparation method and application thereof

A kind of alkaloid and novel technology, applied in the field of novel maca alkaloid and its preparation, can solve the problems of lack of chemical composition and biological activity research of chemical composition

Inactive Publication Date: 2018-04-24
YUNNAN MINZU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0002] Maca ( Lepidium meyenii Walp) (Brassicaceae), known as "Peruvian ginseng" and "South American ginseng", is a 1-2-year-old herb of the genus Brassicaceae. It is native to the South American Andes at an altitude of 3500-4500 m. It is a commonly used local medicine. Using plants and edible materials has a long history and reputation; because Maca is rich in nutrients, rich in protein, carbohydrates, fatty acids, fibers, vitamins and minerals, it is recommended by the United Nations World Food and Agriculture Organization as an edible safe food. In May 2011, maca was also included in the new food resource catalog; modern pharmacological activity studies have shown that maca has a variety of activities beneficial to human health, including improving fertility, anti-oxidation, improving immunity, and improving memory. , memory repair, regulation of hormone release, anti-tumor, blood lipid-lowering, etc. Further studies have shown that some of these biological activities are directly related to their fat-soluble chemical components, such as macaene and macamide, imidazole alkaloids, glucosinolates , sterols and steroids; introduced in China in early 1990, of which the Lijiang Shangri-La region in Yunnan is the main planting area, and the planting scale continues to expand. However, the chemical composition of the introduced Lijiang Maca lacks detailed chemical composition and biological activity research. This patent is Related research on it

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  • Novel Lepidium meyenii Walp. alkaloid, and preparation method and application thereof
  • Novel Lepidium meyenii Walp. alkaloid, and preparation method and application thereof
  • Novel Lepidium meyenii Walp. alkaloid, and preparation method and application thereof

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preparation example Construction

[0022] The preparation method of the alkaloid, the preparation method is based on the cruciferous plant Lepidium maca ( Lepidium meyenii Walp.) rhizome as raw material, obtained by organic solvent extraction, liquid-liquid extraction, MCI de-impurity, silica gel column chromatography, high pressure liquid chromatography extraction and separation steps; the specific steps are:

[0023] A. Organic solvent extraction: The cruciferous plant Lepidium genus Maca ( Lepidium meyenii Walp.) rhizomes are crushed to 20-40 mesh, and ultrasonically extracted 3 to 5 times with an organic solvent, 60 to 120 minutes each time, the extract is filtered and combined; the extract is concentrated by vacuum distillation with a rotary evaporator to obtain maca extract Cream a;

[0024] B. Liquid-liquid extraction: add 1 to 3 times the weight of water to extract a, stir to prepare a suspension, transfer to a separatory funnel or extractor, use the same volume as water and immiscible with water Organic s...

Embodiment 1

[0033] Take the natural air-dried Maca ( Lepidium meyenii Walp.) rhizome, coarsely crushed to 40 mesh, 70% acetone ultrasonic extraction 4 times, 60min each time, the extract is filtered under reduced pressure, combined, and concentrated to 1 / 4 of the volume with a rotary evaporator under reduced pressure; Set, filter off the precipitate and concentrate it into 5.8kg extract a; add 10 kg of water to extract a, extract 5 times with chloroform equal in volume to water, combine the extract phases, and concentrate under reduced pressure to 280g extract b; b. Pack the column with MCI, add 400g of 80% methanol water to the extract b to dissolve it, then load it on the column, eluting with 8-10 liters of 90% methanol water, collect the eluate, and concentrate under reduced pressure to obtain 200g of extract c; Add 450g of acetone to the extract c to dissolve it, then add 300g of 80 mesh silica gel and mix the sample. After mixing the sample, load the column. Pack the column with 200 m...

Embodiment 2

[0035] Take the natural air-dried Maca ( Lepidium meyenii Walp.) rhizome, coarsely crushed to 20 mesh, 80% methanol ultrasonic extraction 5 times, 80 min each time, the extract is filtered under reduced pressure, combined, and concentrated to 1 / 4 of the volume with a rotary evaporator under reduced pressure; Set, filter off the precipitate and concentrate it into 1kg extract a; add 2 kg of water to extract a, extract 5 times with ethyl acetate equal to the volume of water, combine the extract phases, and concentrate under reduced pressure to 50 g extract b; Paste b is packed in MCI column, add 80g of 80% methanol water to extract b to dissolve, then load the column, eluted with 3~5 liters of 80% methanol water, collect the eluate, and concentrate under reduced pressure to obtain 40g extract c ; Add 100g of acetone to the extract c to dissolve, then add 60g of 80 mesh silica gel and mix the sample, after mixing the sample, load the column, use 200 mesh silica gel 400g to pack th...

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Abstract

The invention discloses a novel Lepidium meyenii Walp. alkaloid, and a preparation method and application thereof. The structural formula of the alkaloid is shown in the description, and the alkaloidis a novel hexahydroimidazo[1,5-c]thiazole alkaloid with a formula of C14H14N2O3S2, and is named as (+)-meyeniin A. The preparation method takes rhizome of a cruciferae lepidium plant Lepidium meyeniiWalp. as a raw material, and comprises the steps of organic solvent extraction, liquid-liquid extraction, MCI impurity removal, silica gel column chromatography, high-pressure liquid chromatography and other extraction separation steps for obtaining the alkaloid. The application means application of the alkaloid to anticancer drugs, functional food and health care products. The (+)-meyeniin A shows a certain inhibitory effect on three human tumor cell strains. The alkaloid in the present invention comes from a natural medicine and food dual-purpose plant, has a novel structure, has a potential anti-tumor activity, can be used as an anti-tumor lead compound, and has good application prospects.

Description

Technical field [0001] The invention belongs to the technical field of extraction and separation, structure identification and biological activity research of active ingredients of medicinal plants, and specifically relates to a novel maca alkaloid and its preparation method and application. Background technique [0002] Maca ( Lepidiummeyenii Walp) (Brassicaceae), known as "Peruvian ginseng" and "South American ginseng", is a 1 to 2 year-old herbaceous plant belonging to the cruciferous family Lepidium. It is native to the Andes of South America at an altitude of 3500~4500 m. It is a commonly used medicine locally The use of plants and edible materials has a long history and reputation; because maca is rich in nutrients, rich in protein, carbohydrates, fatty acids, fiber, vitamins and minerals, it is recommended as an edible and safe food by the UN World Food and Agriculture Organization. Maca was also included in the new food resource catalog in May 2011; modern pharmacological...

Claims

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Application Information

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IPC IPC(8): C07D513/04A61K31/429A61P35/00A23L33/105
CPCA23V2002/00C07D513/04A23V2200/308A23V2250/21
Inventor 周敏耿慧春李干鹏胡秋芬杨光宇叶艳青
Owner YUNNAN MINZU UNIV
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