Stilbene compounds in jackfruit dicolor and its use in the preparation of medicines for treating inflammatory diseases
A stilbene, inflammatory disease technology, applied in the field of medicine, can solve problems such as ineffective antibiotic treatment
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] Example 1 Preparation of stilbene compound (±)-dichrome pirolenol E in dichroma jackfruit
[0022] Take 13.9 Kg of jackfruit root, extract by leakage with 95% ethanol, and concentrate the extract under reduced pressure to obtain 1.3 Kg of extract. The extract was suspended in 1 L of water, extracted successively with petroleum ether, chloroform, ethyl acetate and n-butanol (volume ratio 2:1), and concentrated to dryness respectively. Take 118.9 g of the extract from the chloroform extraction part, mix the sample with HP-20 macroporous adsorption resin (weight ratio 1:1), put it on HP-20 type macroporous adsorption resin column (column specification: 10*45 cm), and mix with ethanol-water (0~95%) gradient elution to obtain 6 fractions Frs. H1-H6.
[0023] 50% ethanol eluate fraction Fr. H4 (44.8 g) was subjected to ODS column chromatography (column size: 4*22 cm), MeOH-H 2 O (volume ratio 6:4, 7:3, 8:2, 9:1, 10:0) gradient elution to obtain 15 fractions Frs. H4O1-H4O15....
Embodiment 2
[0024] Example 2 Structural identification of stilbene compound (±)-dichrome pirolenol E in dichroma jackfruit
[0025] (±)-Dichroic pirophenol E is a yellow amorphous powder. HR-ESI-MS gives quasi-molecular ion peaks m / z 395.1855 ([M+H] + , Calculated value: 395.1853), determine its molecular formula as C 24 h 26 o 5 . (±)-Dichroic pirochol E 1 HNMR spectrum (600 MHz, methanol- d 4 ) is highly similar to the known bis-prenyl substituted stilbene hypargystilbene D. Compared with hypargystilbene D, (±)-dichrophenol E has less signal attributed to saturated proton H-5 in hypargystilbene D δ H 5.14. Further comparison of (±)-dichrophenone E and hypargystilbene D 13 CNMR spectrum (150 MHz, methanol- d 4 ) shows that (±)-dichrome porobene E lacks sp in hypargystilbene D 3 The hybridized oxymethine carbon signal C-5 ( δ C 69.5), this signal is replaced by the carbonyl carbon signal δ C 200.0 superseded. This strongly suggests that (±)-dichromobolol E is a ca...
Embodiment 3
[0028] Example 3 Cytotoxicity evaluation experiment of (±)-dichrome pirolenol E on rat PMNs in dichroma jackfruit
[0029] Rat PMNs were isolated and purified using the following experimental procedures. Take clean SD rats (Jiangxi University of Traditional Chinese Medicine Experimental Animal Center, animal qualification certificate number: JZDW2011304), take 9 mL of blood from the orbit, and drop it vertically into a glass centrifuge tube that has been anticoagulated with 1 mL of 1% heparin sodium. Add 4.5% dextran T-500 saline solution at a ratio of 5:1, mix well, and let stand at 4°C for about 1 hour. Take the supernatant, add it to the centrifuge tube pre-filled with lymphocyte separation medium at a ratio of 3:1, 800 rpm (275 g ) Centrifuge for 15 minutes, take out the centrifuge tube, the tube is divided into three layers, the upper layer is light yellow serum, the middle white misty area is monocytes and lymphocytes, and the lower layer is PMNs that settle to the bott...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
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