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

New phloroglucinol compound and applications of new phloroglucinol compound in preparation of antibacterial drugs

A technology of phloroglucinol and antibacterial drugs, which is applied in the field of natural medicines and chemical drugs, can solve the problems of in-depth research, and achieve the effects of low eukaryotic cell toxicity, significant antibacterial activity, and strong activity

Active Publication Date: 2017-07-21
JINAN UNIVERSITY
View PDF2 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the current research on the chemical constituents of myrtle phloroglucinol is not in-depth, and only less than 20 compounds have been reported.
Therefore, its antibacterial active ingredients need to be further explored

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
  • New phloroglucinol compound and applications of new phloroglucinol compound in preparation of antibacterial drugs
  • New phloroglucinol compound and applications of new phloroglucinol compound in preparation of antibacterial drugs
  • New phloroglucinol compound and applications of new phloroglucinol compound in preparation of antibacterial drugs

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Extraction, separation and structural identification of the compound of Example 1

[0031] (1) Take 8 kg of dried myrtle branches and leaves, pulverize them into coarse powder, extract 4 times by percolation with 95% (w / w) ethanol, each 25 L, combine the percolation liquid and concentrate under reduced pressure to no alcohol smell, The obtained total extract is about 1.2kg. The extract was suspended with water and then extracted with petroleum ether to obtain 389 g of petroleum ether extraction fractions.

[0032] (2) Carry out silica gel column chromatography on the petroleum ether extraction part prepared in step (1), using petroleum ether-ethyl acetate as eluent, according to the volume ratio of petroleum ether and ethyl acetate is 100:0, 100:1 , 100:3, 100:5, 100:7, 100:10, 100:30, 100:50, 100:100 and 0:100 elution gradients were eluted, analyzed by thin layer chromatography (TLC) and combined Similar fractions were obtained to obtain 10 main fractions Fr.1-Fr.10....

Embodiment 2

[0048] Example 2 Inhibitory effect of (+) Myrtucyclitones A-B and (-) Myrtucyclitones A-B on various bacteria

[0049] Staphylococcus aureus S.aureus ATCC29213, Methicillin-resistant Staphylococcus aureus S.aureus ATCC33591(MRSA), Vancomycin-intermediate-resistant Staphylococcus aureus S.aureus Mu50(VISA), Staphylococcus epidermidis S.epidermidis ATCC12228 , Enterococcus faecalis ATCC29212, Enterococcus faecalis E.faecium 13-01, Escherichia coli E.coli ATCC25922, Pseudomonas aeruginosa Ps.Aeruginosa, all from the Institute of Medical Biotechnology, Chinese Academy of Medical Sciences.

[0050] The minimum inhibitory concentration (MIC) of the compound in vitro was determined by the broth micro-dilution method. The specific operation method is as follows:

[0051] (1) Bacterial culture: The experimental bacteria were cultured in Mueller-Hinton (MH) broth medium, and when they grew for 8-12 h to a concentration of about 0.5 Mcfarland (1×10 8 CFU).

[0052] (2) The test sample ...

Embodiment 3

[0058] Example 3 Effects of (+) Myrtucyclitones A-B and (-) Myrtucyclitones A-B on normal cells

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 present invention discloses a new phloroglucinol compound and applications of the new phloroglucinol compound in preparation of antibacterial drugs, wherein the structure of the new phloroglucinol compound is represented by a formula I, the new phloroglucinol compound comprises two pairs of enantiomers, and the enantiomers are named (+) Myrtucyclitone A, (-) Myrtucyclitone A, (+) Myrtucyclitone B and (-) Myrtucyclitone B. According to the present invention, the compound has the novel structure, has significant antibacterial activity, can strongly resist Methicillin-resistant Staphylococcus aureus and Vancomycinintermediate-resistant staphylococcus aureus compared to ampicillin and ceftazidime, provides low cytotoxicity to normal cells so as to indicate the good medicinal prospect of the compound, and can be used for preparing antibacterial drugs. The formula I is defined in the specification.

Description

technical field [0001] The invention belongs to the field of natural medicines and chemical medicines, in particular to a new phloroglucinol compound and its application in the preparation of antibacterial medicines. Background technique [0002] Bacterial infection is common disease and frequently-occurring disease. At present, clinical drug-resistant bacterial infections are becoming more and more serious, and bacterial drug resistance is showing a trend towards multidrug resistance. Methicillin-resistant Staphylococcus aureus (MRSA), ampicillin-resistant Streptococcus pneumoniae (PRSP), and multidrug-resistant Drug-resistant tuberculosis (MDR-TB) is spreading rapidly. The increasing number of drug-resistant bacterial infections and the gradual increase in mortality indicate that traditional antibacterial drugs can no longer meet the needs of modern clinical treatment. Therefore, the research and development of new antibacterial drugs has important clinical application v...

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): C07D493/22A61K31/352A61P31/04
CPCC07B2200/07C07D493/22Y02A50/30
Inventor 王磊叶文才刘超
Owner JINAN UNIVERSITY
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