Salvianolic neo-acid compound, preparation method and application thereof

A compound, salvianol technology, applied in the field of natural medicinal chemistry, to achieve the effect of improving blood circulation, inhibiting and scavenging hydroxyl radicals, and having good application prospects

Inactive Publication Date: 2017-03-01
南通市通腾药业有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0005] But, there is no public report about salvianol neo-acid compound of the present invention so far

Method used

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  • Salvianolic neo-acid compound, preparation method and application thereof
  • Salvianolic neo-acid compound, preparation method and application thereof
  • Salvianolic neo-acid compound, preparation method and application thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0031] The preparation of embodiment 1 salvianolic acid

[0032] After 20 kg of dried salvia miltiorrhiza (S. miitiurrhizu) was sliced, 10 times the volume (V / W) of the medicinal material (V / W), namely 200 kg of 50% ethanol solvent, was heated and extracted at 70° C. for 3 times for 0.5 hours each time to obtain an extract. The extract is concentrated under reduced pressure at a pressure of 10-98Kpa and a temperature of 60-70°C to prepare 40L of a concentrated solution. Add water to dilute to 80L, filter, and extract three times with equal volume of ethyl acetate to remove fat-soluble components. Concentrated under reduced pressure to 3L, the concentrated solution was mixed with an equal amount of silica gel, separated by silica gel column chromatography, and sequentially eluted with chloroform:methanol:formic acid (6:1:0.01-4:1:0.01) gradient to obtain fraction 1 , Fraction 2, Fraction 3, Fraction 4, Fraction 5; Fraction 5 was separated with Sephadex LH-20, and methanol: wat...

Embodiment 2

[0033] The preparation of embodiment 2 salvianolic acid

[0034] After 20 kg of dried salvia miltiorrhiza (S. miitiurrhizu) was sliced, 5 times the volume (V / W) of the medicinal material (V / W), namely 100 kg of 90% ethanol solvent, was heated and extracted twice at 20° C. for 1 hour each time to obtain an extract. The extract is concentrated under reduced pressure at a pressure of 10-98Kpa and a temperature of 50-60°C to prepare 40L of a concentrated solution. After diluting to 80L with water, extract three times with an equal volume of dichloromethane to remove fat-soluble components. Concentrated under reduced pressure to 3L, the concentrated solution was mixed with an equal amount of silica gel, separated by silica gel column chromatography, and sequentially eluted with chloroform:methanol:formic acid (6:1:0.01-4:1:0.01) gradient to obtain fraction 1 , Fraction 2, Fraction 3, Fraction 4, Fraction 5; Fraction 5 was separated with Sephadex LH-20, and methanol: water (9:1-3:7...

Embodiment 3

[0035] The preparation of embodiment 3 salvianolic acid

[0036] After 20 kg of dried salvia miltiorrhiza (S. miitiurrhizu) were sliced, 8 times the volume of the medicinal material (V / W), that is, 160 kg of pure water, was heated and extracted once at 90° C. for 2 hours each time to obtain an extract. Add 160L of alcohol to the extract, place and filter, and concentrate the extract under reduced pressure at a pressure of 10-98Kpa and a temperature of 80-90°C to make 40L of concentrated solution. After diluting to 80L with water, extract three times with an equal volume of dichloroethane to remove fat-soluble components. Concentrated under reduced pressure to 3L, the concentrated solution was mixed with an equal amount of silica gel, separated by silica gel column chromatography, and sequentially eluted with chloroform:methanol:formic acid (6:1:0.01-4:1:0.01) gradient to obtain fraction 1 , Fraction 2, Fraction 3, Fraction 4, Fraction 5; Fraction 5 was separated with Sephadex...

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Abstract

The invention discloses a salvianolic neo-acid compound shown in a structural formula (I), 2 bite and 3 bite of a benzo tetrahydrofuran unit in the compound are cis configuration. The invention also discloses a preparation method and an application of the salvianolic neo-acid compound. The salvianolic neo-acid compound has obvious anti-lipid peroxidation effect, has obvious effect for inhibiting and removing hydroxyl radical, is very suitable for treating acute and chronic cardio cerebrovascular diseases such as coronary heart disease, and has good application prospect for preventing and treating neurodegenerative diseases such as senile dementia.

Description

technical field [0001] The invention relates to the technical field of natural medicine chemistry, in particular to a salvianolic acid compound extracted and separated from dried salvia miltiorrhiza (S. miitiurrhizu) and its preparation method and application. Background technique [0002] Salvia miltiorrhiza is one of the most commonly used medicinal materials in traditional Chinese medicine. It has many functions such as dispelling blood stasis and relieving pain, promoting blood circulation and stimulating menstruation, clearing heart and eliminating troubles. The results of research in recent years have shown that the antibacterial effect of Salvia miltiorrhiza is mainly fat-soluble components, and the role of promoting blood circulation and removing blood stasis is mainly water-soluble components. Water-soluble salvianolic acids are the main active components of Salvia miltiorrhiza, which have anti-lipid peroxidation , antithrombotic, improving blood circulation, etc., ...

Claims

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Application Information

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Patent Type & AuthorityApplications(China)
IPC IPC(8): C07D307/84A61K31/343A61P9/00A61P25/28A61P25/16A61P39/06A61P7/02
CPCC07D307/84
Inventor沈征武
Owner南通市通腾药业有限公司