CN102532211A - Lignan triglycoside compound and preparation method and application thereof - Google Patents
Lignan triglycoside compound and preparation method and application thereof Download PDFInfo
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- CN102532211A CN102532211A CN201110433164XA CN201110433164A CN102532211A CN 102532211 A CN102532211 A CN 102532211A CN 201110433164X A CN201110433164X A CN 201110433164XA CN 201110433164 A CN201110433164 A CN 201110433164A CN 102532211 A CN102532211 A CN 102532211A
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Abstract
The invention discloses a lignan triglycoside compound and a preparation method and application thereof. The molecular formula of the lignan triglycoside compound is C38H56O22. The preparation method comprises the following steps of: placing crushed Castanea henryi (Skan) Rehd.et Wils husks into an organic solvent for extraction, separating to prepare the extract solution, extracting the extract solution, and preparing the extract via concentration of the extract solution; and carrying out chromatographic separation and purification of the extract to prepare the lignan triglycoside compound. The organic solvent is one or mixture of methanol, ethanol, butanol and acetone. The lignan triglycoside compound with the novel structure is prepared via extraction and separation of the Castanea henryi (Skan) Rehd.et Wils husk, has good antioxidant activity, can be applied in preparation of antioxidants, antioxidant drugs, antioxidant cosmetics or antioxidant health food, and has good development prospect.
Description
Technical field
The present invention relates to the active components of plants field, relate in particular to a kind of lignanoid three glycoside compounds.
Background technology
Chinquapin (Castanea henryi (Skan) Rehd.et Wils) is a Fagaceae Castanea plant, is famous woody grain in China south and fruit material dual-purpose seeds, and fruit is fragrant and sweet good to eat, and local flavor obviously is superior to Chinese chestnut.Chinquapin is the most concentrated in the Mountain Area in North resource distribution of south, Zhejiang; And have big area artificial forest ((a) river by. the river is all. Gao Rixia. the chinquapin new cultivation technology. Foochow: Fujian science tech publishing house, 1998.1-19. (b) Zheng Chengle. the river is by. the north of Fujian Province chinquapin resource and utilize prospect. the journal .1998 of Fujian Agricultural Univeristy, 27 (3): 291-295. (c) Gong Bangchu. Chen Zenghua. the research of chinquapin farm variety resource exploration. forestry scientific research; 1997; 10 (6): 574-580. (d) Yang Zhiling, Gong Bangchu, Chen Zenghua. the quantification analysis of chinquapin Fruit Economic Traits. forestry scientific research; 2001,14 (1): 90-94.).
At present, less about the chemical constitution study of chinquapin, depleted Exocarpium Castanopsis chinensis particularly, the current utilization that almost is only limited to fertilizer.For this reason, the active skull cap components in the research Exocarpium Castanopsis chinensis can provide new approaches for the recycling of Exocarpium Castanopsis chinensis.
Summary of the invention
The invention provides a kind of lignanoid three glycoside compounds, this compound is to extract the natural active matter that obtains in the shell of chinquapin, has anti-oxidant activity.
A kind of lignanoid three glycoside compounds, its structural formula is suc as formula shown in (I):
The invention provides the preparation method of described lignanoid three glycoside compounds, may further comprise the steps:
(1) chinquapin (Castanea henryi (Skan) Rehd.et Wils) shell after will pulverizing places the organic solvent lixiviate, separates obtaining vat liquor, vat liquor is extracted again, and extraction liquid obtains extract after concentrated;
Wherein, described organic solvent is one or more mixtures in methyl alcohol, ethanol, propyl carbinol and the acetone;
(2) extract is carried out chromatographic separation, purification process, make described lignanoid three glycoside compounds.
In the step (1), described Exocarpium Castanopsis chinensis pulverized to be placed on carry out lixiviate in the organic solvent, more help the leaching of lignanoid's three glycoside compounds.
The weight ratio of described Exocarpium Castanopsis chinensis and organic solvent is preferably 1: 1-1: 8.
Described lixiviate can be cold soaking or thermal backflow extraction.
The reagent of said extraction usefulness can be propyl carbinol.
In the step (2), preferably, described chromatographic separation is the purification on normal-phase silica gel column chromatography for separation, and eluent is the chloroform/methanol mixed solution; More preferably, in the described purification on normal-phase silica gel column chromatography for separation: after going up appearance, as eluent, carried out gradient elution in 9: 1 by volume, 5: 1,1: 1,1: 3,1: 9, collect the cut that 5: 1 o'clock wash-outs of eluent volume ratio go out with the chloroform/methanol mixed solution.
Described purification process can separate or performance liquid chromatography separates for: recrystallization, reversed-phase silica gel column chromatography.Through purifying, can obtain the higher lignanoid of purity three glycoside compounds.
Preferably, the isolating eluent of said reversed-phase silica gel column chromatography is the methanol mixed solution; More preferably, during described reversed-phase silica gel column chromatography separates: after going up appearance, as eluent, carried out gradient elution in 9: 1 by volume, 5: 1,1: 1,1: 3,1: 9 with the methanol mixed solution.
The present invention also provides the application of described lignanoid three glycoside compounds in the preparation inhibitor.Lignanoid of the present invention three glycoside compounds can directly use as inhibitor; Perhaps, be one of main active ingredient or activeconstituents with lignanoid of the present invention three glycoside compounds, process inhibitor after the interpolation acceptable auxiliary and use.
The present invention also provides the application of described lignanoid three glycoside compounds in the preparation anti-oxidation medicine.This medicine is a main active ingredient with lignanoid of the present invention three glycoside compounds, and acceptable auxiliary is processed on the interpolation pharmaceutics, can process preparation according to the formulation preparation method of putting down in writing on the pharmaceutics.Described preparation can be for injection liquid, drip liquid, powder injection, granule, tablet, electuary, powder, oral liquid, sugar coated tablet, film coated tablet, enteric coated tablet, suck agent, granule, pill, paste, sublimed preparation, sprays, pill, disintegrating agent, oral cavity disintegration tablet, micropill etc.
The present invention also provides the application of described lignanoid three glycoside compounds in preparation antioxidation cosmetic article.These makeup are main active ingredient with lignanoid of the present invention three glycoside compounds, add acceptable makeup auxiliary material and process.
The present invention also provides described lignanoid three glycoside compounds in preparation anti-oxidation health Application in Food.This protective foods is a main active ingredient with lignanoid of the present invention three glycoside compounds, adds acceptable protective foods auxiliary material and processes.
The present invention extracts from Exocarpium Castanopsis chinensis, separate and obtained a kind of lignanoid's three glycoside compounds with novel structure, and this method is easy and simple to handle, extract that yield is high, product purity is high, is fit to large-scale production.
Through the antioxidation in vitro test, show that lignanoid provided by the invention three glycoside compounds have better antioxidation, its IC
50Value is 11 μ M, can be used for preparing inhibitor, anti-oxidation medicine, antioxidation cosmetic article or anti-oxidation health food, has the excellent development prospect.
Description of drawings
Fig. 1 is a compound among the embodiment 6
1H
1H COSY, the relevant collection of illustrative plates of HMBC.
Embodiment
The preparation of embodiment 1 lignanoid three glycoside compounds
Get 5kg chinquapin (Castanea henryi (Skan) Rehd.et Wils) shell, pulverize, soaked for 2 weeks with methyl alcohol, with 1L zero(ppm) water suspendible, aqueous suspension is used the 1L n-butanol extraction to soak solution after concentrating, and butanol extraction liquid obtains medicinal extract through concentrating; (100 orders 100g) are mixed appearance, carry out purification on normal-phase silica gel column chromatography for separation (200-300 order, 1kg with silica gel; Silicagel column size L 500mm;
); Carry out gradient elution with 9: 1,5: 1,1: 1,1: 3,1: 9 chloroform/methanol of volume ratio successively, each 5L; TLC detects cut, collects 5: 1 cut of wash-out ratio and merges, and uses recrystallizing methanol again.
The preparation of embodiment 2 lignanoids three glycoside compounds
Get the 5kg Exocarpium Castanopsis chinensis, pulverize, use the 5L alcohol reflux, extracting solution concentrates, and aqueous suspension is used the 1L chloroform extraction, and chloroform layer discards, and water layer is used the 1L n-butanol extraction; The propyl carbinol partially concd, (100 orders 100g) are mixed appearance, carry out purification on normal-phase silica gel column chromatography for separation (200-300 order, 1kg with silica gel; Silicagel column size L 500mm;
); Carry out gradient elution with 9: 1,5: 1,1: 1,1: 3,1: 9 chloroform/methanol of volume ratio successively, each 5L; TLC detects cut, collects 5: 1 cut of wash-out ratio and merges, and uses recrystallizing methanol again.
The preparation of embodiment 3 lignanoids three glycoside compounds
Get the 5kg Exocarpium Castanopsis chinensis, pulverize, extract with 5L methanol/ethanol mixed solution, extract concentrates, and mixes appearance with 100g zeyssatite, and 5L propyl carbinol heat is extracted; Carry out purification on normal-phase silica gel column chromatography for separation (200-300 order, 1kg; Silicagel column size L 500mm;
); Carry out gradient elution with 9: 1,5: 1,1: 1,1: 3,1: 9 chloroform/methanol mixed solution of volume ratio successively, each 5L; TLC detects cut, collects 5: 1 cut of wash-out ratio and merges, and uses acetone/normal hexane (volume ratio 1: 1) recrystallization again.
The preparation of embodiment 4 lignanoids three glycoside compounds
Get the 5kg Exocarpium Castanopsis chinensis, pulverize, extract with 5L methanol/ethanol mixed solution, extract concentrates, and mixes appearance with 100g zeyssatite, and 5L propyl carbinol heat is extracted; Carry out purification on normal-phase silica gel column chromatography for separation (200-300 order, 1kg; Silicagel column size L 500mm;
); Carry out gradient elution with 9: 1,5: 1,1: 1,1: 3,1: 9 chloroform/methanol mixed solution of volume ratio successively, each 5L; TLC detects cut, collects 5: 1 cut of wash-out ratio and merges; Cut separates with reversed-phase silica gel column chromatography/performance liquid chromatography, and eluent is that (9: 1-1: 9), the detection wavelength of performance liquid chromatography is 254nm to methanol; Use recrystallizing methanol.
The preparation of embodiment 5 lignanoids three glycoside compounds
Get the 5kg Exocarpium Castanopsis chinensis; Pulverize, extract with 5L methanol/ethanol/acetone mixed solution, extract is concentrated into does not have the alcohol flavor; Use the 5L n-butanol extraction; Extraction liquid concentrates, and goes up macroporous resin (size L 500mm,
) behind the water suspendible and removes sugar; Ethanol washes the back and concentrates, and the 100g silica gel mixed sample carries out purification on normal-phase silica gel column chromatography for separation (200-300 order, 1kg; Silicagel column size L 500mm;
); Carry out gradient elution with 9: 1,5: 1,1: 1,1: 3,1: 9 chloroform/methanol mixed solution of volume ratio successively, each 5L; TLC detects cut, collects 5: 1 cut of wash-out ratio and merges; Cut separates with reversed-phase silica gel column chromatography/performance liquid chromatography, and eluent is that (9: 1-1: 9), the detection wavelength of performance liquid chromatography is 254nm to methanol; Use recrystallizing methanol.
The structure of embodiment 6 lignanoids three glycoside compounds is identified
Adopt HPLC that the compound that makes is carried out purity and identify, purity is carried out the structure evaluation greater than 98% sample utilization mass spectrum and nuclear magnetic resonance technique, and nucleus magnetic resonance is measured with Bruker AVANCE DRX-500NMR Sectrometer, mark in TMS does; High resolution mass spectrum FTICRMS measures with Bruker Apex Spectrometer; Electrospray ionization mass spectrum ESI-MS is with Bruker Esquire 3000
PlusSpectrometer measures.
According to the one-dimensional NMR analytical results (seeing table 1) and the two-dimentional NMR analytical results (see figure 1) of compound, can know that this material is lignanoid's three glycoside compounds, molecular formula is C
38H
56O
22, structure is as follows:
The NMR data of table 1 lignanoid three glycoside compounds
aRecorded?on?125MHz.
bMultiplicities?inferred?from?DEPT?and?HMQC?experiments.
cRecorded?on?500MHz.
Embodiment 7 lignanoids three glycoside compounds anti-oxidant activities are analyzed
Get a certain amount of sample, be dissolved in absolute ethyl alcohol, be made into concentration 5mM solution; Dilute one by one with absolute ethyl alcohol, dilute five times at every turn; Get 96 hollow plates, every hole adds ethanolic soln (150 μ M) the 180 μ l of DPPH; The sample solution that adds 5 concentration then successively, each concentration 4 hole, every hole adds 20 μ l; Rock 96 orifice plates a little, let it mix; Place thermostat container, 37 ℃ leave standstill 30min; Measure the OD value in every hole respectively at 517nm and 800nm with ELIASA; Using the Bliss method to obtain the DPPH clearance rate is 50% o'clock sample concentration, and promptly half is removed experiment.
Remove experimental result by DPPH and know the IC of this compound
50=11 μ M show that this compound has better antioxidation.
Embodiment 8 contains the preparation of lignanoid's three glycoside compounds dropping pill formulations
Get 0.5g lignanoid three glycoside compounds and 10.5g polyoxyethylene glycol-6000 and mix, heating and melting moves in the dripping pill drip irrigation behind the change material, and in ℃ whiteruss of medicine liquid droplet to 6～8, oil removing makes 300 of dripping pills.
Embodiment 9 contains the preparation of lignanoid's three glycoside compounds lyophilized injectable powders
Get the three glycoside compounds 0.5g of lignanoid, glucose 4.5g, Sulfothiorine 0.9g and zero(ppm) water 1000ml, after said components mixes, lyophilize, 400 of packing promptly get.
Claims (7)
1. lignanoid's three glycoside compounds, its structural formula is suc as formula shown in (I):
2. the preparation method of lignanoid as claimed in claim 1 three glycoside compounds is characterized in that, may further comprise the steps:
(1) chinquapin (Castanea henryi (Skan) Rehd.et Wils) shell after will pulverizing places the organic solvent lixiviate, separates obtaining vat liquor, vat liquor is extracted again, and extraction liquid obtains extract after concentrated;
Wherein, described organic solvent is one or more mixtures in methyl alcohol, ethanol, propyl carbinol and the acetone;
(2) extract is carried out chromatographic separation, purification process, make the described lignanoid of claim 1 three glycoside compounds.
3. preparation method according to claim 2 is characterized in that, in the step (1), the weight ratio of described Exocarpium Castanopsis chinensis and organic solvent is 1: 1-1: 8.
4. preparation method according to claim 2 is characterized in that, in the step (2), described chromatographic separation is the purification on normal-phase silica gel column chromatography for separation, and eluent is the chloroform/methanol mixed solution.
5. preparation method according to claim 2 is characterized in that, in the step (2), described purification process is: recrystallization, reversed-phase silica gel column chromatography separate or performance liquid chromatography separates.
6. preparation method according to claim 5 is characterized in that, the isolating eluent of said reversed-phase silica gel column chromatography is the methanol mixed solution.
7. lignanoid as claimed in claim 1 three glycoside compounds are in preparation inhibitor, anti-oxidation medicine, antioxidation cosmetic article or anti-oxidation health Application in Food.
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109019742A (en) * | 2018-07-11 | 2018-12-18 | 李玉茹 | A kind of sewage-treating agent and preparation method thereof of efficient absorption heavy metal |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2006061115A (en) * | 2004-08-30 | 2006-03-09 | Kiyomoto Bio Co Ltd | Method for producing sesaminol by fermentation process |
| CN101773490A (en) * | 2010-01-25 | 2010-07-14 | 香港理工大学深圳研究院 | Active part of Sambucus williamsii Hance for reducing risk of bone-related diseases of menopausal women and application thereof |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006061115A (en) * | 2004-08-30 | 2006-03-09 | Kiyomoto Bio Co Ltd | Method for producing sesaminol by fermentation process |
| CN101773490A (en) * | 2010-01-25 | 2010-07-14 | 香港理工大学深圳研究院 | Active part of Sambucus williamsii Hance for reducing risk of bone-related diseases of menopausal women and application thereof |
Non-Patent Citations (5)
| Title |
|---|
| 《J. Agric. Food Chem.》 20080726 YOUNG-WON CHIN et al. Lignans and Other Constituents of the Fruits of Euterpe oleracea (A�ai) with Antioxidant and Cytoprotective Activities 7759-7764 1、7 第56卷, 第17期 * |
| KUO-CHING JAN ET AL.: "Tissue distribution and elimination of sesaminol triglucoside and its metabolites in rat", 《MOL. NUTR. FOOD RES.》 * |
| LIYA LI ET AL.: "Maple Syrup Phytochemicals Include Lignans, Coumarins, a Stilbene, and Other Previously Unreported Antioxidant Phenolic Compounds", 《J. AGRIC. FOOD CHEM.》 * |
| YOUNG-WON CHIN ET AL.: "Lignans and Other Constituents of the Fruits of Euterpe oleracea (Açai) with Antioxidant and Cytoprotective Activities", 《J. AGRIC. FOOD CHEM.》 * |
| YOUNG-WON CHIN ET AL.: "Lignans and Other Constituents of the Fruits of Euterpe oleracea (Açai) with Antioxidant and Cytoprotective Activities", 《J. AGRIC. FOOD CHEM.》, vol. 56, no. 17, 26 July 2008 (2008-07-26), pages 7759 - 7764 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109019742A (en) * | 2018-07-11 | 2018-12-18 | 李玉茹 | A kind of sewage-treating agent and preparation method thereof of efficient absorption heavy metal |
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