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

Applications of phenylmercuric acetate in serving as indoleamine 2,3-dioxygenase-1 inhibitor

A technology of phenylmercuric acetate and dioxygenase, which is applied in the application field of diseases, can solve the problems that laboratory or clinical effects need to be improved, the number of IDO1 inhibitors is small, and the like

Inactive Publication Date: 2016-11-09
SUN YAT SEN UNIV
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the overall number of IDO1 inhibitors is still small, and the laboratory or clinical effects still need to be improved

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
  • Applications of phenylmercuric acetate in serving as indoleamine 2,3-dioxygenase-1 inhibitor
  • Applications of phenylmercuric acetate in serving as indoleamine 2,3-dioxygenase-1 inhibitor
  • Applications of phenylmercuric acetate in serving as indoleamine 2,3-dioxygenase-1 inhibitor

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0015] The present invention will now be further explained in conjunction with the following experiments and accompanying drawings. It should be noted that these experimental examples and accompanying drawings should not be construed as limiting the present invention.

[0016] Kynurenine standard curve drawing

[0017] 1. Standard medium (200 μL): 20 μL of 0.5M potassium phosphate buffer (pH 6.5), with a final concentration of 50 mM; 20 μL of 0.2M ascorbic acid, with a final concentration of 20 mM; 4 μL of 0.5 mM methylene blue, with a final concentration of 10 μM; 4 μL of 5 mg / ml catalase to a final concentration of 100 μg / ml; 132 μL of dd-H 2 O; 20 μL of kynurenine solution with final concentrations of 0, 1, 5, 7.5, 10, 25, 50, 75 and 100 mM.

[0018] 2. After adding 40μL of 1M NaOH solution, centrifuge the medium (11,500rpm, 4°C, 15min).

[0019] 3. Transfer 200 μL of the supernatant to a 96-well microtiter plate and measure the fluorescence intensity (λex 360nm, λem480nm...

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 provides applications of phenylmercuric acetate or pharmaceutically acceptable salt of phenylmercuric acetate in serving as an indoleamine 2,3-dioxygenase-1 (IDO1) inhibitor, namely, the inhibiting effect of phenylmercuric acetate for indoleamine 2,3-dioxygenase-1, phenylmercuric acetate has the function of hindering and / or destroying the acceleration effect of IDO1 in the generation and development processes of diseases, and thus good prospects are provided for treating IDO1-mediated diseases.

Description

technical field [0001] The present invention relates to the new use of phenylmercuric acetate as indoleamine 2,3-dioxygenase-1 (IDO1) and its application in preparation and treatment of diseases mediated by IDO1. Background technique [0002] Indoleamine 2,3-dioxygenase-1 [EC 1.13.11.17] (IDO1) is an intracellular, monomeric heme-containing protein that catalyzes the catabolism of l-tryptophan (Trp) into canine The first step of the uridine pathway. The IDO1 metabolite, N-formylkynurenine, is further metabolized into other bioactive molecules. IDO1 is expressed in multiple tissues, including lung, small intestine, placenta, spleen and central nervous system. IDO1 can be expressed in many cell types stimulated by inflammatory cytokines (such as interferon gamma, Escherichia coli endotoxin and tumor necrosis factor-α, etc.). IDO1 is also expressed in host antigen-presenting cells (APCs), monocyte-macrophages, and tumor cells. [0003] IDO1 has been regarded as an important...

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 Applications(China)
IPC IPC(8): A61K31/305A61P35/00A61P9/00A61P25/18A61P25/16A61P25/28A61P27/12
CPCA61K31/305
Inventor 李庆王忠
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