Rhuschalcone compounds and application thereof

A bis-chalcone and compound technology, applied in the application field of this type of compound, can solve the problems that the research results have not been paid attention to, and achieve the effect of good antifungal effect and remarkable effect

Inactive Publication Date: 2012-08-22
CENTRAL SOUTH UNIVERSITY OF FORESTRY AND TECHNOLOGY
View PDF1 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In 1998, Italian scholar Artico synthesized a series of bis-chalcone analogues and found that they had good activity of inhibiting HIV integrase in vitro (Artico et al., Journal of medicinal chemistry, 1998, 41(21): 3948-3960), but their research The results were not taken seriously

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
  • Rhuschalcone compounds and application thereof
  • Rhuschalcone compounds and application thereof
  • Rhuschalcone compounds and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Preparation of compound 1-6 (see Table 1 for specific structural formula): acetophenone derivative (0.02mol), m-phthalaldehyde or terephthalaldehyde (0.01mol), absolute ethanol 18mL, thionyl chloride 1.8mL Add it into a 100mL three-neck flask, react at room temperature for 2-8 hours, monitor the reaction by TLC (thin layer chromatography), stop the reaction until the reaction is complete, and add 10mL distilled water to aid precipitation. Vacuum filter, wash with a large amount of cold distilled water, then wash the product once with 100 mL of ethanol at 65°C to remove impurities, filter while hot, and dry in vacuum at 60°C to obtain the product.

[0036] m-Hydroxyacetophenone and m-phthalaldehyde prepare 3'-hydroxyl-3-(3-(3-hydroxyphenyl)-3-carbonyl-propenyl)chalcone (compound 1) according to Example 1, yield : 42.54%, Mp: 239.7-241.9°C. 1 HNMR (CD 3 COCD3, δ, ppm): 7.130, 7.136, 7.150, 7.156 (dd, 2H, J = 8.0, 2.4Hz, 4, 6-H), 7.389, 7.409, 7.429 (6.923, 6.945 (d, 4H,...

Embodiment 2

[0043] Preparation of Compound 7-11 (see Table 1 for specific structural formula): Acetophenone derivatives (0.01mol), terephthalaldehyde or m-phthalaldehyde (0.005mol), absolute ethanol 20mL, 10mL 10% NaOH ( W / V) into a 100mL three-neck flask, react at room temperature for 1-5 days, add 50mL of distilled water, neutralize with 3M HCl to pH = 6, filter under reduced pressure, dry the filter residue, use silica gel column chromatography, and recrystallize. Dry to obtain the product.

[0044] 2-Hydroxyl-6-methoxymethoxyacetophenone and terephthalaldehyde prepare 2'-hydroxyl-6'-methoxymethoxyl-4-(3-(2-hydroxyl-6- Methoxymethoxyphenyl)-3-carbonyl-propenyl)chalcone (compound 7), yield 14.01%. MP: 190.4-192.0°C. 1 H NMR (CDCl 3 , δ, ppm): 3.541 (s, 6H, 6×H-CH 3 ), 5.323(s, 4H, 4×H-CH 2 ), 6.605, 6.625 (d, 2H, J=8.0, 2×3′-H), 6.672, 6.674, 6.693, 6.695 (dd, 2H, J=8.2Hz, 2×5′-H), 7.343, 7.364 , 7.385(t, 2H, J=8.4Hz, 2×4′-H), 7.662(s, 4H, 1×2, 3, 5, 6-H), 7.789, 7.828(d, J=15.6Hz...

Embodiment 3

[0054] Embodiment 3 antibacterial activity

[0055] After the test bacteria were taken out from the refrigerator at 4°C, they were inoculated on the medium of the petri dish: the bacteria were inoculated on the beef extract peptone medium, and cultured at 37°C for 24 hours; the mold was inoculated on the PDA medium, and cultivated at 28°C for 48 hours. stand-by. Then, the 13 compounds synthesized were made into 5 gradient concentrations (2500 μg / mL, 1000 μg / mL, 500 mg / mL, 250 μg / mL, 100 μg / mL) with ethyl acetate, and were added to each petri dish by casting method. 9mL of sterilized culture medium and 1mL of sample were used, and the control group was replaced by 1mL of ethyl acetate and sterile water, and the other was the same. The medium was solidified and then inoculated with a 6mm hole punch. Then put them into a constant temperature and humidity incubator for cultivation, with bacteria at 37°C and fungi at 28°C. When the colony on the control group was about to cover ...

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 relates to Rhuschalcone compounds and application of the Rhuschalcone compounds. The compounds have two alpha, beta- ketene active structures, and have the specific general formula shown in formula (I) or (II), wherein R1, R2, R3, R4 and R5 are independently selected from hydrogen, hydroxy, C1-C6 alkoxy or methoxyl. The invention also relates to the application of the compounds in the aspect of preparing a wood preservation preparation and the aspect of preparing an oxidation resistant preparation.

Description

technical field [0001] The present invention relates to a class of bis-chalcones, which have two α, β-enone structures. The invention also relates to the application of such compounds. Background technique [0002] The basic structure of chalcones is 1,3-diphenylpropenone (see formula a), which widely exists in nature, such as licorice, hops, Oxytropis falciparum. Due to the greater flexibility of the molecules of chalcones, they can bind to different receptors, so they have a variety of biological activities, such as antibacterial, anti-oxidation, anti-cancer, anti-inflammatory, anti-parasitic, anti-viral, therapeutic Diabetes, neuroprotection, anti-gastric ulcer (Zhang Yanwen, Foreign Medicine. Pharmacy Volume, 1996 (04): 218-223). Chalcones have a variety of biological activities, and are derived from natural sources with high safety. Therefore, chalcones are used as lead compounds to modify their structures and develop chalcone analogs with specific biological activiti...

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): C07C49/835C07C49/84A01N35/04C09K15/06B27K3/38A01P3/00
CPCC09B23/143A01N35/04B27K3/38C09K15/06
Inventor 李湘洲旷春桃郭远良
Owner CENTRAL SOUTH UNIVERSITY OF FORESTRY AND TECHNOLOGY
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

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap