Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Application of moving point motor protein small molecular inhibitor to inhibition of tumor cell proliferation

A technology of tumor cell proliferation and motor protein, which is applied in the field of small molecule inhibitors of kinetochore motor protein in inhibiting tumor cell proliferation. issues such as stable phenotypes

Active Publication Date: 2012-07-11
姚雪彪 +1
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Loss of CENP-E inactivates the spindle checkpoint, leading to errors in chromosome movement and segregation resulting in chromosomal instability phenotypes

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 moving point motor protein small molecular inhibitor to inhibition of tumor cell proliferation
  • Application of moving point motor protein small molecular inhibitor to inhibition of tumor cell proliferation
  • Application of moving point motor protein small molecular inhibitor to inhibition of tumor cell proliferation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0067] Embodiment 1, the synthesis of target compound formula VII:

[0068]

[0069] (Formula XV) (Formula VII)

[0070] Add 1mmol 5a, the compound shown in 1.1mmol intermediate formula XV (its synthetic reference document Monatshefte fuer Chemie, 127 (5), 549-555,1996) in the three-necked flask, in 10ml THF, add 2mmol K under stirring 2 CO 3 , heated to reflux, monitored by TLC until the reaction was complete, cooled, filtered with suction, recovered the solvent under reduced pressure, dissolved the obtained residue in chloroform, washed with water, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was recovered by suction filtration, and the residue was recrystallized from isopropanol / dichloromethane to obtain the pure product of the target compound of formula VII.

[0071] figure 1 It is the nuclear magnetic detection spectrogram of the pure product formula VII compound (named as Syntelin), A is the carbon spectrum, and B is the nitroge...

Embodiment 2

[0085] Embodiment 2, the synthesis of target compound formula III:

[0086]

[0087] (Formula XIV) (Formula III)

[0088] Add 1mmol 5b, the compound shown in 1.1mmol intermediate formula XIV (its synthetic reference Bioorganic & Medicinal Chemistry Letters 16 (17), 4444-4449, 2006) in the three-necked flask, in 10ml THF, add 2mmol K under stirring 2 CO 3 , heated to reflux, monitored by TLC until the reaction was complete, cooled, filtered with suction, recovered the solvent under reduced pressure, dissolved the obtained residue in chloroform, washed with water, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was recovered by suction filtration, and the residue was recrystallized from isopropanol / dichloromethane to obtain the pure product of the target compound represented by formula III.

[0089] Wherein, compound 5b is prepared according to the following steps:

[0090] 1) Synthesis of intermediate 1b:

[0091]

[0092] For the syn...

Embodiment 3

[0102] Embodiment 3, the synthesis of target compound formula VIII:

[0103]

[0104] (Formula XV) (Formula VIII)

[0105] Add 1mmol 5a, the compound shown in 1.1mmol intermediate formula XV (its synthetic reference document Monatshefte fuer Chemie, 127 (5), 549-555,1996) in the three-necked flask, in 10ml THF, add 2mmol K under stirring 2 CO 3 , heated to reflux, monitored by TLC until the reaction was complete, cooled, filtered with suction, recovered the solvent under reduced pressure, dissolved the obtained residue in chloroform, washed with water, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was recovered by suction filtration, and the residue was recrystallized from isopropanol / dichloromethane to obtain the pure product of the target compound formula VIII.

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

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
Login to View More

Abstract

The invention discloses an application of a moving point motor protein small molecular inhibitor to inhibition of tumor cell proliferation. The moving point motor protein small molecular inhibitor is a compound shown as a formula I or a formula II, and is named Syntelin. As proved by animal experiments, the Syntelin shown as a formula VII can be used for remarkably inhibiting the growth of human breast cancer cells. As proved by further mechanism experiments, the Syntelin shown as the VII formula can be used for inhibiting the walk of a CENP-E (Centromere Protein-E) motor on a micro-tube without influencing the interaction between the CENP-E and the micro-tube after being combined with the CENP-E. When the compound is added into a cell culture medium, the compound can enter cells to inhibit the function of the CENP-E, so that a part of chromosomes are arranged wrongly, and the activity of a spindle detection point is maintained for a long time. The CENP-E small molecular inhibitor Syntelin disclosed by the invention plays an important role in cell biology researches, and a basis can be laid for the research of novel chemotherapy medicaments by using the function of the inhibitor for controlling tumor cell proliferation. The formula I, formula II and formula VII are shown in the specifications.

Description

technical field [0001] The invention relates to the application of small molecular inhibitors of motor protein in inhibiting tumor cell proliferation. Background technique [0002] The precise self-replication of cells is an important part of life activities, and the high conservation of replication plays an important role in the reproduction of organisms and species. During the process of cell replication, the parental genetic information contained in the chromosomes is equally and accurately distributed to the two daughter cells after undergoing many complex movements. Cell cycle events are carried out in a highly orderly manner, and the biochemical regulatory pathways that ensure the orderly progress of the cell cycle are called "checkpoints". [0003] Kinetochores are multicomponent protein complex structures located at centromeres. It not only directly maintains the connection between the spindle filament and the chromosome, but also regulates the temporal and spatial...

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): A61K31/519A61P35/00
CPCA61K31/675C07D495/04C07F9/6561A61K31/519A61P35/00A61P43/00
Inventor 姚雪彪杨志宏万卫红姚彧丁霞张健存
Owner 姚雪彪
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products