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

Multiple target point furanone-quinolinone compounds and preparation method and usage of multiple target point furanone-quinolinone compounds

A technology of furanone and quinolinone, which is applied in the application field of preparing antibacterial drugs, to achieve the effect of good inhibition and killing effect and high antibacterial activity

Active Publication Date: 2015-05-27
枣庄市天源药业有限公司
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There are no dual-target antibacterial compounds targeting TyrRS and type II topoisomerase

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
  • Multiple target point furanone-quinolinone compounds and preparation method and usage of multiple target point furanone-quinolinone compounds
  • Multiple target point furanone-quinolinone compounds and preparation method and usage of multiple target point furanone-quinolinone compounds
  • Multiple target point furanone-quinolinone compounds and preparation method and usage of multiple target point furanone-quinolinone compounds

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Example 1: 3-(2-chlorophenyl)-4-(4-(1-cyclopropyl-3-carboxy-6-fluoro-4-quinolinone-7-yl)piperazin-1-yl )-2(5H)-furanone (7)

[0024] Step 1: Dissolve 1.9g of sodium 2-chlorophenylacetate in 20mL of DMSO, add 1.8mL of ethyl bromoacetate at room temperature, heat up to 35°C and react for 8 hours. After the reaction is complete, dilute with ethyl acetate, wash with water, and wash the organic layer with Wash with saturated brine until neutral, dry, concentrate, use silica gel column chromatography, eluent is petroleum ether-AcOEt, the volume ratio of petroleum ether and AcOEt is 7:1, obtain 2.3g oily 2-(2-chlorophenylacetyl Oxy) ethyl acetate;

[0025] Step 2: Dissolve 2.0 g of ethyl 2-(2-chlorophenylacetoxy)acetate in a constant-pressure funnel containing 10 mL of anhydrous THF, add 0.21 g of NaH into a flask containing 5 mL of anhydrous THF, A THF solution of ethyl 2-(2-chlorophenylacetoxy)acetate was added slowly with stirring. Stir the reaction at room temperature f...

Embodiment 2

[0037] Embodiment 2: the antibacterial activity of compound

[0038]Bacteria were suspended in MH medium at a concentration of approximately 10 5 cfu mL -1 , add the bacterial solution to a 96-well plate (100 μL of bacterial solution per well), use the culture medium as a blank control, use DMSO instead of a test substance as a negative control, use penicillin G as a positive control for Gram-positive bacteria, and use penicillin G as a positive control for Gram-positive bacteria. Kanamycin was used as a positive control for Shi-negative bacteria, and ketoconazole was used as a positive control for fungi. Dissolve the test substance in DMSO to prepare 1600, 800, 400, 200, 100, 50 μg·mL -1 solution (for MIC 50 Less than 5μg·mL -1 Yes, when carrying out one-step experiment, the prepared concentration gradient is 100, 50, 25, 12.5, 6.25 μg·mL -1 ), was added to a 96-well plate at an amount of 11 μL per well, and four parallel experiments were performed for each concentration...

Embodiment 3

[0041] Example 3: Extraction of TyrRS and determination of the activity of compounds on TyrRS

[0042] TyrRS from Staphylococcus aureus was expressed in E. coli and purified by Sephadex chromatography. The activity of TyrRS was determined by aminoacylation reaction. The enzyme reaction mixture consists of the following components: 100mM TrisHCl pH7.9, 50mM KCl, 16mM MgCl 2 , 5mM ATP, 3mM dithiothreitol, 4mg / mL Escherichia coli MRE600tRNA and 10μM[ 3 H] Tyrosine (activity 1.48-2.22TBq / mmol). Mix and incubate TyrRS (0.2nM) and different concentrations of test substances at room temperature for 10 minutes, then add an equal amount of the above enzyme reaction mixture preheated to 37°C, and after co-incubating for 5 minutes, add an equal volume of 7% glacial trichloro Acetic acid solution was used to terminate the reaction, filtered through a 96-well Millipore filter plate, and the filtrate was detected by a scintillation counter, and each sample was repeated 4 times. The one ...

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 furanone-quinolinone compounds which have the following structural general formula. The furanone-quinolinone compounds have good inhibiting effects on staphylococcus epidermidis, pneumonia Klebsiella, Cryptococcus neoformans and the like, and can be used for preparing anti-infection drugs for treating intestinal infection, pneumonia, wound suppuration and the like. The invention further discloses a preparation method of the furanone-quinolinone compounds.

Description

technical field [0001] The invention relates to a preparation method of a class of furanone-quinolinone compounds and their application in the preparation of antibacterial drugs. technical background [0002] The rapid spread of drug-resistant bacteria makes the treatment of bacterial infections more and more difficult. It has been clinically shown that bacterial resistance poses a threat to almost all antimicrobials. From the late 1980s to the 1990s, extended-spectrum β-lactamases ( ESBLs) and inducible β-lactamases (AmpC enzymes) can hydrolyze most β-lactams including oxyiminos (cefetazidime, ceftriaxone, cefotaxime, aztreonam, etc.) Amide antimicrobials. Most strains producing ESBLs are multi-drug resistant strains, which are also resistant to fluoroquinolones. According to relevant reports, fluoroquinolones have different degrees of drug resistance to Enterococcus, Klebsiella, Escherichia coli, Streptococcus pneumoniae, etc., and there is a high degree of cross-resist...

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 Patents(China)
IPC IPC(8): C07D471/04C07D405/12C07D405/14A61P31/04
Inventor 肖竹平王旭东杜秀芳
Owner 枣庄市天源药业有限公司
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