Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Aromatic acid compound and application

A technology of compounds and acids, applied in the field of medicine, can solve the problems of no methyl mandelate and the like

Inactive Publication Date: 2014-07-23
SHENYANG PHARMA UNIVERSITY
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, according to the literature survey on the chemical constituents of peach kernels, there is no report about methyl mandelate

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Aromatic acid compound and application
  • Aromatic acid compound and application
  • Aromatic acid compound and application

Examples

Experimental program
Comparison scheme
Effect test

experiment example 1

[0026] Experimental example 1 Structural identification experiment of methyl mandelate

[0027] The structure of the mandelate methyl ester prepared in Examples 1-3 can be identified using this experimental example.

[0028] White powder (methanol), ESI-MS m / z : 513.05[M+Na] + , 529.05[M+K] + , according to which the molecular weight is determined to be 490.05, combined with 1 H-NMR and 13 C-NMR data, deduce that this compound molecular formula is C 21 h 30 o 13 . 1 H-NMR (300 MHz, CD 3 OD) spectrum, δ : 7.38(2H, m), 7.54 (3H, m) are characteristic hydrogen signals of monosubstituted benzene, δ :5.48(1H, s) is the benzyl hydrogen signal, δ : 4.28(1H, d, J = 7.6Hz), 4.45(1H, d, J = 7.6Hz) are the signals of 2 sugar anogroup protons, δ : 3.71(3H, s) is the methoxyl proton signal; 13 C-NMR (75Mz, CD 3 OD) spectrum, δ : 173.3 is the carboxyl carbon signal, and 104.8 and 101.4 are the sugar terminal carbon signals. Comparing the carbon and hydrogen dat...

experiment example 2

[0031] Experimental example 2 Scopolamine-induced memory loss in mice

[0032] (1) Experimental materials

[0033] 1. Experimental animals

[0034] ICR mice, male, weighing 18-22 g, were provided by the Experimental Animal Center of Shenyang Pharmaceutical University, license number: SCXK (Beijing) 2009-0004.

[0035]2. Drugs and reagents

[0036] Test drug: methyl mandelate, dissolved with 0.5% CMC-Na before administration, and made into a solution.

[0037] Scopolamine Hydrobromide Injection: Shanghai Hefeng Pharmaceutical Co., Ltd., production batch number: 080701, the dose for mice is 3 mg / kg; Naofukang, Hubei Huazhong Pharmaceutical Co., Ltd., batch number: 20091224.

[0038] Equipment: platform jumper, self-made.

[0039] (2) Experimental method

[0040] 1. Grouping and administration

[0041] The ICR mice were randomly divided into 5 groups according to body weight, namely blank control group, model group, positive control group, high-dose and low-dose groups...

Embodiment 1

[0051] Embodiment 1: Get 1kg of peach kernel medicinal material, pulverize, adopt 70% ethanol aqueous solution to reflux extract at 80 ℃ for 4h, extract is concentrated under reduced pressure to obtain concentrate; Butanol extraction, ethanol, 70% ethanol and 95% ethanol gradient elution; 30% ethanol eluate, concentrated under reduced pressure, dried, and silica gel column chromatography, using volume ratios of 9:1, 8:2, 7 :3, 6:4, 5:5 dichloromethane-methanol mixed solvent elution, and then separated and purified by preparative HPLC, with acetonitrile-water with a volume ratio of 95:5 as mobile phase elution to obtain mandelate A Esters 20mg.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention belongs to the field of medicine, and relates to an aromatic acid compound isolated from the dry mature seeds of Viaceae plant peach Prunuspersica (L.) Batsch or mountain peach Prunusdavidiana (Carr.) Franch. application in medicine. The compound of the present invention has the following structure, and is obtained through the steps of extraction, concentration, extraction, concentration and purification, and the compound has obvious protective effect on Aβ(25~35)-induced neuroblastoma cell line SH-SY5Y damage , has the effect of preventing and treating senile dementia.

Description

technical field [0001] The invention relates to an aromatic acid monomer compound and its application, belonging to the technical field of medicine. Background technique [0002] Alzheimer's disease (Alzheimer's disease, AD) was first discovered by the neuropathologist Alzheimer in 1906 and named after him. AD is a diffuse central neurodegenerative disease, a common senile neurodegenerative disease characterized by progressive cognitive impairment, mental decline, and personality changes, accounting for about 50% to 60% of all dementias. According to reports, about 3% of the elderly aged 65-74 suffer from AD, and the prevalence rate of the population aged 75-84 is 19%, while the prevalence of AD among the elderly aged > 85 is higher than 47%. The fourth leading cause of death in the elderly. Although there is a lack of authoritative and representative statistics for developing countries, it is estimated that 60% of the world's dementia patients exist in developing coun...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07H15/18C07H1/08A61K31/7028A61P25/28
Inventor 毕开顺贾英李清黄健范旭航沈旭
Owner SHENYANG PHARMA UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com