Unlock instant, AI-driven research and patent intelligence for your innovation.

Schiff alkali ligand of ruthenium, preparation method and application thereof

A technology of complexes and alkali ligands, applied in the field of anti-cancer drugs, to achieve the effects of simple preparation methods and post-processing methods, obvious anti-tumor activity, and good crystal form stability

Inactive Publication Date: 2018-06-29
SHAANXI SCI TECH UNIV
View PDF10 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In recent years, there have been some reports on the antitumor activity of Schiff base complexes, but there are few reports on the effect of complexes formed by platinum metals and Schiff base compounds on tumor cells.

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
  • Schiff alkali ligand of ruthenium, preparation method and application thereof
  • Schiff alkali ligand of ruthenium, preparation method and application thereof
  • Schiff alkali ligand of ruthenium, preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Mix acetonitrile and isopropanol in a volume ratio of (1-5): 2 to obtain a mixed solvent 1;

[0030] The mixed solvent 2 is obtained by mixing ethanol and isopropanol at a volume ratio of 1: (1-5).

[0031] Mixed solvent 3 was obtained by mixing methanol and acetonitrile at a volume ratio of 1:3.

Embodiment 2

[0033] 2 mmol of 5-chlorosalicylaldehyde and 1 mmol of N-cyclohexyl-1,3-propanediamine were dissolved in 1 mL of mixed solvent 1 for aldol condensation reaction to obtain Schiff base ligand compound 1.

Embodiment 3

[0035] 2 mmol of 5-chlorosalicylaldehyde and 1 mmol of N-cyclohexyl-1,3-propanediamine were dissolved in 5 mL of mixed solvent 2 for aldol condensation reaction to obtain Schiff base ligand compound 2.

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 a Schiff alkali ligand for ruthenium, a preparation method and application thereof. The preparation method comprises the following steps: heating and dissolving ruthenium saltwith stirring in a mixed solvent to obtain a solution 1; heating and dissolving the Schiff alkali ligand in the mixed solvent to obtain a solution 2, stopping the heating on the solution 2, and cooling the solution 2 to room temperature, adding the solution 1 into the solution 2 to obtain a solution 3; continually stirring the solution 3 at room temperature for 0.5 to 1.0h, standing the solution 3in a high-pressure reaction kettle, heating and cooling the solution 3 through program control to obtain a Schiff alkali ligand of the ruthenium being of a brick-red crystal appearance. The Schiff alkali ligand of ruthenium provided by the invention has the advantages of high crystal form stability, relative simple preparation method and post treatment manner, capability of being applied to the tumor activity resistant aspect and remarkable tumor resistance, as well as is taken as an important basis for the subsequent researching of the anti-tumor medicines.

Description

technical field [0001] The invention belongs to the technical field of anticancer drugs, in particular to a Schiff base complex of ruthenium and its preparation method and application. Background technique [0002] Cisplatin is a commonly used drug for the treatment of cancer. Its anti-tumor mechanism mainly uses DNA as the main target, destroys DNA replication and inhibits cell division to inhibit the growth of tumor cells. However, the long-term use of cisplatin drugs has the disadvantages of large toxic and side effects, strong drug resistance and narrow anticancer spectrum. [0003] However, the development of metal complexes represented by cisplatin has successfully promoted the development and research of anticancer drugs, and promoted the development of metal complexes in the entire medical field. Metal complexes, especially some Schiff base metal complexes, because these compounds contain functional functional groups, have some physical and chemical properties requi...

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): C07F15/00A61K31/555A61P35/00
CPCC07F15/0053
Inventor 卢久富季晓晖葛红光靳玲侠赵蔡斌郑楠岳思羽郭小华杨海涛曹小燕
Owner SHAANXI SCI TECH UNIV