Curcumin analogues and preparation and application thereof

A kind of curcumin analog, the technology of the analog, applied in the intermediate of synthesizing the curcumin analog and its preparation, the application field of anti-tumor drugs, can solve the problems such as low water solubility, rapid metabolism, poor stability, etc. Activity and selectivity enhancing effects

Active Publication Date: 2016-02-24
SHENYANG PHARMA UNIVERSITY
View PDF1 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, curcumin also has defects such as low water solubility, poor stability, and rapid metabolism in the body.

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
  • Curcumin analogues and preparation and application thereof
  • Curcumin analogues and preparation and application thereof
  • Curcumin analogues and preparation and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Preparation of Example 11-(3,4-dimethoxyphenyl)-3,5-diketone-1-hexene (A1)

[0044] Acetylacetone (16.3 mL, 160 mmol) and diboron trioxide (7.8 g, 112 mmol) were added to 100 mL of ethyl acetate, and the temperature was raised to 70° C. for 0.5 h. 3,4-Dimethoxybenzaldehyde (13.2g, 80mmol) and tri-n-butyl borate (21.6mL, 80mmol) were added slowly, and reacted at 70°C for 0.5h. Add 10 mL of ethyl acetate to 8 mL of n-butylamine, and dropwise complete. Reaction at 100°C for 1.5h. Cool down to 60°C, add 50mL of 0.4mol L -1 Hydrochloric acid, reaction 0.5h. After the reaction was completed, cool to room temperature, wash with water, extract the aqueous layer with ethyl acetate (30 mL×3), combine the organic phases, wash with saturated sodium chloride solution, and dry over anhydrous sodium sulfate. After filtration and concentration under reduced pressure, the obtained oil was separated and purified by column chromatography (eluent was petroleum ether-ethyl acetate). 6....

Embodiment 2

[0045] Example 21-(3,4-dimethoxyphenyl)-7-(3-methoxy-4-hydroxyphenyl)-1,6-heptadiene-3,5-dione (A2) preparation of

[0046] 6-(3,4-dimethoxyphenyl)hex-5-ene-2,4-dione (10.0 g, 40.3 mmol) (A1) and diboron trioxide (4.8 g, 68.5 mmol) were added Into 160 mL of ethyl acetate, the temperature was raised to 70° C. for 0.5 h. Add 3-methoxy-4-hydroxybenzaldehyde (6.1g, 40.3mmol) and tri-n-butyl borate (18.4g, 79.0mmol) slowly, and react at 70°C for 0.5h. Piperidine (4mL, 40.5mmol) was added dropwise, and after the drop was completed, the temperature was raised to 100°C and reacted for 1.5h. Then cool down to 60°C, add 80mL of 0.4mol·L -1 Hydrochloric acid, reacted for 0.5h, after the reaction was completed, cooled to room temperature, washed with water, extracted the aqueous layer with ethyl acetate (30mL×3), combined the organic phases, washed with saturated sodium chloride solution, and dried over anhydrous sodium sulfate. After filtration and concentration under reduced pressur...

Embodiment 3

[0047] Example 31-(3,4-dimethoxyphenyl)-7-(3-methoxy-4-acetoxyphenyl)-1,6-heptadiene-3,5-dione ( A3) Preparation

[0048] 1-(3,4-dimethoxyphenyl)-7-(3-methoxy-4-hydroxyphenyl)-1,6-heptadiene-3,5-dione (A2) ( 5.0g, 13.1mmol), acetic anhydride (3.0mL, 32.8mmol) and pyridine (2.6mL, 32.8mmol) were added to 50mL of dichloromethane, and refluxed for 5h. After the reaction was completed, it was cooled to room temperature, adjusted to neutral pH with saturated aqueous sodium bicarbonate solution, and dried over anhydrous sodium sulfate. After filtration and concentration under reduced pressure, a yellow solid was obtained, which was recrystallized from ethyl acetate and petroleum ether to obtain 4.8 g of a yellow solid, with a yield of 86.4%. m.p.133-136℃, ESI-MS, m / z: 425.2[M+H] + .

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 medical technology and relates to preparation and application of a series of curcumin analogues. The curcumin analogues have structures as shown in the formula I, formula II and formula III, wherein R, R1 and R2 are as mentioned in the specification. Pharmaceutically acceptable salt and solvate of the curcumin analogues and a medicine containing the curcumin analogues or the pharmaceutically acceptable salt used as active components can be used in treatment of cancer. The curcumin analogues and the pharmaceutically acceptable salt have a good anticancer activity. A preparation method of the curcumin analogues is simple and feasible and is easy to operate.

Description

Technical field: [0001] The invention relates to a new curcumin analogue and a preparation method thereof, and also relates to an intermediate for synthesizing the curcumin analogue, a preparation method thereof and an application as an antitumor drug. Background technique: [0002] Turmeric is a perennial herb of the genus Curcuma longa. It is recorded in "Compendium of Materia Medica" that turmeric is named Baodingxiang, and its smell is pungent, bitter, severe cold, and non-toxic. It is used for the treatment of unbearable heartache and abdominal pain due to fetal cold. Curcumin is the most important active ingredient of turmeric to exert pharmacological effects and has a wide range of pharmacological effects. Studies have shown that curcumin has obvious inhibitory effects on human gastric cancer, liver cancer, leukemia and other cancers and has little toxic and side effects (Cui Shuxiang, Jin Dongqing, Zhou Ling, etc. Experimental observation of curcumin's anti-tumor ef...

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): C07D295/088C07C213/04C07C217/20A61K31/5377A61K31/496A61K31/4545A61K31/4025A61K31/138A61K31/40A61K31/5375A61K31/495A61K31/4453A61P35/00A61P35/02
CPCY02P20/55
Inventor 张美慧曹亮夏明钰徐莉英张平董金华
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
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