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

Polyacid compound for resisting penicillin streptococcus pneumoniae (PRSP) and preparing method thereof

A technology of Streptococcus pneumoniae and polyacid compounds, which is applied in the field of chemical synthesis of drugs and their preparation, and can solve problems such as the rise of bacteria and the loss of efficacy of antibiotics

Inactive Publication Date: 2009-02-11
NORTHEAST NORMAL UNIVERSITY
View PDF1 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The rising incidence of Streptococcus pneumoniae resistance to penicillin (drug resistance mechanism is the change of penicillin-binding protein PBP2′), making many antibiotics gradually lose their original effectiveness

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
  • Polyacid compound for resisting penicillin streptococcus pneumoniae (PRSP) and preparing method thereof
  • Polyacid compound for resisting penicillin streptococcus pneumoniae (PRSP) and preparing method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0013] Synthesis Example 1

[0014] The compound formed by amantadine and Keggin type phosphomolybdic acid [(C 10 h 18 N) 3 PMo 12 o 40 ·xH 2 O] Synthesis: Dissolve 100 g of amantadine in 200 ml of water, acidify with dilute hydrochloric acid to a pH of about 6, and add dropwise to the aqueous solution containing 402 g of phosphomolybdic acid under constant stirring. With the addition of amantadine, the solution gradually became cloudy and finally produced a large amount of precipitate. Continue stirring for 1 h to make the reaction complete, separate the precipitate by suction filtration, wash twice with distilled water, then wash with ethanol, and dry in the air to obtain a yellow powder as (C 10 h 18 N) 3 PMo 12 o 40 ·nH 2 O. The yield was 85% based on amantadine.

[0015] Synthesis Example 2

[0016] Amantadine and LnW 10 o 36 9- (Ln is a lanthanide) compound (C 10 h 18 N) 9 wxya 10 o 36 ·xH 2 Synthesis of O: Dissolve 100g amantadine in 200ml water, ...

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 belongs to the field of chemically synthesized medicine and its preparation process. The medicine of the present invention is synthesized with amantadine, moroxydine, 5-Fu (5-Fc), isoniazid and other clinical medicine and polyoxometallate, and through self-assembling. The said polyoxometallate includes heteropoly acid salts of Keggin type with chemical expression XM12O40n-, Dowson type X2M18O62n- and of chemical expression LnW10O36n-. The combined use of said medicines and polyoxometallate has obvious curative effect on intractable streptococcus pneumoniae infection.

Description

technical field [0001] The invention belongs to chemically synthesized drugs and a preparation method thereof, in particular to polyacid antibacterial drugs capable of inhibiting penicillin-resistant Streptococcus pneumoniae (PRSP) and a preparation method thereof. Background technique [0002] Streptococcus pneumoniae belongs to Gram-positive bacteria and is one of the most important pathogens of severe invasive infections (such as meningitis, sepsis, acute otitis media, sepsis, pneumonia) and upper respiratory tract infections. Globally, 4 to 6 million people die each year from this bacterial infection. It was once considered that penicillin was a routine sensitive drug for Streptococcus pneumoniae. Since the first reports of penicillin-resistant Streptococcus pneumoniae (PRSP, penicilline-resistant streptococcuspneumoniae) infection in Australia and South Africa in the 1960s and 1970s, PRSP infection has There have been reports all over the world, and surveys have shown ...

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): C07F3/00C07F11/00A61K31/66A61K31/555A61K31/28A61P31/04
Inventor 刘术侠白云鹏翟红菊杜宏明李德惠梁大栋
Owner NORTHEAST NORMAL 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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com