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

Application of tiacumicin derivative to preparation of medicine for treating related diseases and/or symptoms caused by dengue virus infection

A technology of taigamycin and dengue virus, applied in the field of medicine, can solve the problem of lack of effective drugs, etc., and achieve the effects of high safety, strong binding ability, and high activity of inhibiting dengue virus

Active Publication Date: 2018-02-23
SUN YAT SEN UNIV +1
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] At present, there is a lack of clinically approved effective drugs against dengue virus

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 tiacumicin derivative to preparation of medicine for treating related diseases and/or symptoms caused by dengue virus infection

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Example 1: Anti-DENV activity of tiacumicin derivatives at the cellular level

[0022] Virus strain: Dengue virus DENV2 (NGC)

[0023] Cell line: A549

[0024] Detection method:

[0025] Tiacumicin derivative antiviral half effective dose (50% Effective Concentration, EC 50 ): DMSO, gradient concentrations of tiacumicin derivatives to saturate the cells 1 h in advance, after 2 h of virus infection, replace the virus-free medium containing the corresponding concentration of drugs for 48 h; collect the cell supernatant, extract the viral RNA in the supernatant, and use qRT- PCR method was used to detect the copy number of DENV2 virus RNA in the supernatant.

[0026] Inhibition rate (%) = (1-viral RNA copy number of drug administration group / viral RNA copy number of solvent control group) 100%, calculated using the Forcast formula of EXCEL 2013, when the inhibition rate is equal to 50%, corresponding to tiacumicin derivative The concentration of the substance, as EC 5...

Embodiment 2

[0031] Example 2 The inhibitory activity of tiacumicycin derivatives to DENV2-prM protein in A549 cell line

[0032] Virus strain: Dengue virus DENV2 (NGC)

[0033] Cell line: A549

[0034] Detection method:

[0035] DMSO, 1, 5, 10 μM tiacumicin derivatives were used to saturate the cells 1 hour in advance, and 2 hours after the virus infection, the virus-free medium containing the corresponding concentration of drugs was replaced for 48 hours; the cell pellet was collected, and the cells under different treatments were detected by western blot electrophoresis The relative expression of internal DENV2 (NGC)-prM protein, with GAPDH as internal reference protein. Such as figure 1 . Tiacumicin derivatives Compound 1 and Compound 2 can effectively inhibit the expression of DENV2prM protein at a concentration of 1-5 μM. As an important structural protein, the expression of DENV2prM protein is inhibited, which means that the reproduction of DENV2 has been inhibited.

Embodiment 3

[0036] Example 3 Surface plasmon resonance detection of affinity between tiacumicin derivatives and DENV2-NS5 protein

[0037] This method adopts GE's Biacore T100 instrument and CM5 chip for experiments. First, the purified DENV2 (NGC)-NS5 protein is amino-coupled to the CM5 chip, and then flows through different concentrations of tiacumicin derivatives, and the instrument detects The mass change of the substance adsorbed on the surface of the chip is calculated to calculate the affinity rate of the compound (K a ) vs. dissociation rate (K d ). Affinity = dissociation equilibrium constant (K D ), this value describes the binding strength between a small molecule and a protein molecule. The biological meaning is that when a small molecule binds to a protein 1:1, let 50% of the small molecule saturate the concentration of the protein molecule. The smaller the value, the stronger the binding. Usually, the affinity between small molecules and proteins calculated by this method...

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 an application of a tiacumicin derivative to preparation of a medicine for treating related diseases and / or symptoms caused by dengue virus infection. Tiacumicin serving as a clostridium difficile infection resisting medicine clinically approved for use is high in safety, and the tiacumicin derivative can remarkably inhibit dengue viruses, is high in activity, has strong binding capacity with dengue virus non-structural protein NS5 and can be expected to be a novel effective dengue virus infection resisting medicine.

Description

technical field [0001] The invention belongs to the field of medicine, and more specifically relates to the application of tiacumicycin derivatives in the preparation of medicines for treating related diseases and / or symptoms caused by dengue virus infection. Background technique [0002] Tiacumicins (Tiacumicins) is a general term for a series of 18-membered macrolide antibiotics, and is an important class of therapeutic antibiotics. [0003] Dengue virus belongs to the Flaviviridae family and is an RNA positive-strand virus. It is transmitted by mosquitoes and can cause symptoms such as generalized fever, rash, and arthritis. In severe cases, it can cause shock and death. [0004] DENV-NS5 is an RNA-dependent RNA polymerase that performs the function of viral genome replication and plays a crucial role in viral replication. Inhibition of this enzyme activity can achieve the effect of killing dengue virus. [0005] Currently, there is a lack of clinically approved effecti...

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): A61K31/7048A61P31/14
CPCA61K31/7048Y02A50/30
Inventor 黎孟枫袁洁朱勋于暕辰张海波朱义广张光涛
Owner SUN YAT SEN UNIV
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