Preparation method of natural biflavones such as I3,II8-Biapgienin and Ridiculuflavone A

A biflavone, natural technology, applied in the preparation of new compounds and the field of medicine, can solve the problems of limited activity research, scarce sources, etc., and achieve the effect of a wide range of biological activities and simple purification methods

Active Publication Date: 2017-03-22
TIANJIN UNIV OF SCI & TECH
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the scarcity of its source, research on its activity is limited

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
  • Preparation method of natural biflavones such as I3,II8-Biapgienin and Ridiculuflavone A
  • Preparation method of natural biflavones such as I3,II8-Biapgienin and Ridiculuflavone A
  • Preparation method of natural biflavones such as I3,II8-Biapgienin and Ridiculuflavone A

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0019] In order to understand the present invention, the present invention will be further described below in conjunction with embodiment; Following embodiment is illustrative, not limiting, can not limit protection scope of the present invention with following embodiment.

[0020] The present invention provides compounds 1 and 2

[0021]

[0022] The present invention specifically includes compounds:

[0023] (1) 5,5',7,7'-tetrahydroxy-2,2'-bis(4-hydroxyphenyl)-4H,4'H-[3,8'-dibenzopyran]-4 ,4'-Diketone

[0024] (2) 2'-(3,4-dihydroxyphenyl)-5,5',7,7'-tetrahydroxy-2-(4-hydroxyphenyl)-4H,4'H-[3,6 '-Dibenzopyran]-4,4'-dione

[0025] Synthetic routes of compounds 1 and 2

[0026]

[0027] Description 1

[0028] 5,5',7,7'-tetrahydroxy-2,2'-bis(4-hydroxyphenyl)-4H,4'H-[3,8'-dibenzopyran]-4,4' - dione

[0029] Add 2.0 g (0.010 mol) of 2-hydroxy-4,6-dimethoxyacetophenone and 2.0 g (0.012 mol) of 4-isopropoxybenzaldehyde into 3 mL of ethanol and stir for 5 min. Then 6ml o...

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 present invention belongs to the field of new compound preparation methods and medicine research, and particularly relates to a preparation method of natural biflavones such as I3,II8-Biapgienin and Ridiculuflavone A. According to the present invention, the two compounds such as I3,II8-Biapgienin and Ridiculuflavone A are firstly synthesized, wherein I3,II8-Biapgienin has good anti-depression activity, good anti-tumor activity, good anti-oxidation activity, good anti-inflammatory activity and good anti-liver injury activity, further has inhibition activity on estrogen receptors, benzodiazepine receptors and CYP, and has broad prospects in the fields of drug development and application.

Description

technical field [0001] The invention belongs to the field of novel compound preparation method and medicine, especially the preparation of natural biflavone compounds I3, II8-Biapgienin and RidiculuflavoneA. Background technique [0002] I3,II8-Biapgienin is a biflavonoid compound extracted from Hypericum perforum L. Hypericum perforum is also known as St. John's Wort in Europe and the United States. Hypericum perforatum is used in Germany The treatment of depression has a history of hundreds of years. It has been reported that I3, II8-Biapgienin has good antidepressant, antitumor, antioxidative, anti-inflammatory, and anti-liver damage activities, and also has effects on estrogen receptors and benzodiazepines. Body and CYP have inhibitory activity, and have broad prospects in drug development and application. [0003] Ridiculuflavone A is a natural biflavone compound extracted from Aristolochia ridicula, a plant of the potato family. Due to the scarcity of its source, the...

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 Applications(China)
IPC IPC(8): C07D311/30
CPCC07D311/30
Inventor 郁彭杨柯马艳涛潘国军李明芦逵王栋
Owner TIANJIN UNIV OF SCI & TECH
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
Try Eureka
PatSnap group products