Application of phenyl ether compound with antitumor activity

A compound, phenyl ether technology, applied in the application field of phenyl ether compounds as anti-tumor drugs, can solve the problem of no reports of anti-tumor drugs and the like

Inactive Publication Date: 2015-03-18
中国中化股份有限公司 +1
View PDF7 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] The compound of the present invention has been disclosed in patents CN1887847A, CN101119961A, WO2007000098A, US7947734A, KR100

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
  • Application of phenyl ether compound with antitumor activity
  • Application of phenyl ether compound with antitumor activity
  • Application of phenyl ether compound with antitumor activity

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0071] Example 1: For the growth inhibition rate of human bladder cancer cells J82, LNCap, T24, and prostate cancer cell PC-3, about 1000 to 3000 cells were planted in a 24-well plate using in vitro cell culture technology, and then each well was Add 1 ml of cell culture medium well known to those skilled in the art that can cultivate the tumor cell lines used in the test, and place in a cell culture incubator (CO 2 5%, 370°C) for 24 hours, then add an appropriate concentration of the above-mentioned substance to be tested into the wells, and note that the volume of the added solution does not exceed 0.5% of the total volume. Let the cells continue to grow in the cell culture incubator. After one week, aspirate the cell culture medium and wash once with cold 1 ml PBS. Then, fix with 1% formalin at room temperature for 10 minutes, and wash once with cold 1 ml PBS. Add 0.1% crystal violet to stain for 30 minutes. Crystal violet recycling. The stained cells were washed slowly ...

Embodiment 2

[0079] Example 2: For the growth inhibition rate of human leukemia HL-60 cells, the conventional MTT method was used to measure the inhibition rate of the test samples on the growth of each human cancer cell. The cells were taken out from the incubator, washed twice with PBS solution, digested with 0.25% trypsin solution, and a medium well-known to those skilled in the art capable of cultivating tumor cell lines for testing was added to stop the digestion of each cell line, and after centrifugation, Pipette to form a cell suspension and count under an inverted microscope. And use the medium for cultivating each cancer cell line to prepare the cells to a concentration of 5x10 4 / ml of cell suspension, add 100 μl of cells to each well of a 96-well plate, place it in 5% carbon dioxide, and incubate overnight in humidified air at 37°C, add the above-mentioned drugs to be tested diluted into different concentration gradients, and let it act for 48 hours. MTT was added, and after 4 ...

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 discloses an application of a phenyl ether compound as shown in general formula I in preparation of antitumor drugs. The compound of the general formula I has very good antitumor activity, and especially has excellent activity for human bladder cancer LNCap, T24, J82 and human prostate cancer PC-3.

Description

technical field [0001] The invention belongs to the field of medicine and relates to the field of antitumor drugs. It specifically relates to the application of phenyl ether compounds as antitumor drugs. Background technique [0002] The compound of the present invention has been disclosed in patents CN1887847A, CN101119961A, WO2007000098A, US7947734A, KR100963911A, JP2008546815A, and has bactericidal and acaricidal activities, but there is no report on its application as an antitumor drug. Contents of the invention [0003] The object of the present invention is to provide the application of the phenyl ether compounds with the structure shown in the general formula I in the preparation of antitumor drugs. [0004] Technical scheme of the present invention is as follows: [0005] The application of phenyl ether compounds as antineoplastic drugs, such as fluoxastrobin, enoxastrobin, azoxystrobin, bifujunzhi, picoxystrobin ), pyraclostrobin, triclopyricarb, fenaminstrobin...

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
IPC IPC(8): A61K31/539A61K31/505A61K31/44A61K31/415A61K31/165A61P35/00A61P35/02
CPCA61K31/539A61K31/165A61K31/216A61K31/415A61K31/44A61K31/505
Inventor 关爱莹杨小平柴宝山迟会伟李淼刘长令
Owner 中国中化股份有限公司
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