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

Applications of 9-methyl-3,6-diacetylcarbazole in treating or preventing respiratory inflammatory diseases

A technology for diacetylcarbazole and inflammatory diseases, applied in the field of PI3Kγ specific inhibitors, can solve the problems of limited efficacy of drugs for respiratory inflammatory diseases

Active Publication Date: 2019-04-12
CF PHARMTECH
View PDF3 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In summary, traditional drugs for the treatment of respiratory inflammatory diseases have limited effects, and rational drug design based on PI3Kγ targets can provide new and efficient drugs for the treatment of respiratory diseases

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 9-methyl-3,6-diacetylcarbazole in treating or preventing respiratory inflammatory diseases
  • Applications of 9-methyl-3,6-diacetylcarbazole in treating or preventing respiratory inflammatory diseases
  • Applications of 9-methyl-3,6-diacetylcarbazole in treating or preventing respiratory inflammatory diseases

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Embodiment 1: PI3K inhibition rate detected by in vitro enzyme experiment;

[0022] The inhibitory activity of the compound 9-methyl-3,6-diacetylcarbazole on PI3Kα, PI3Kβ, PI3Kδ, and PI3Kγ was detected using the ADP-Glo ​​kit.

[0023] The broad-spectrum PI3K inhibitor PI-103 was used as a positive control.

[0024] PI3Kγ blank group: use a 96-well plate to set up 3 parallel experimental groups. Prepare 10 μl of PI3K reaction system, each well contains 2.5 μL of PI3Kγ protein, add 2.5 μL of reaction substrate PIP2 to start the reaction, incubate at room temperature for 1 hour, use 5 μL of MgCl 2 The reagent terminated the reaction, and after incubation for 2 hours, 10 μL of ADP-Glo ​​detection reagent was added, and after incubation for 45 minutes, the fluorescence value of the reaction solution was detected by a microplate reader.

[0025] Use the same operation to prepare PI3Kα, PI3Kβ, PI3Kδ blank groups

[0026] PI3Kγ experimental group: use a 96-well plate and se...

Embodiment 2

[0033] Example 2: Detecting the inhibitory effect of compounds on the expression of pro-inflammatory cytokine TNFα;

[0034] ELISA kits were used to detect the content of TNFα in inflammatory cells.

[0035] (1) Take mouse mononuclear macrophages (RAW264.7 cells) in the logarithmic growth phase, inoculate 1 mL of 5000 cells per well on a 6-well plate, set up blank control group, LPS (lipopolysaccharide) group, and positive drug (LY294002)+LPS control group, 9-methyl-3,6-diacetylcarbazole+LPS group.

[0036] (2) The blank control group was not treated; the LPS group was treated with 1 μg / mL LPS; the LY294002 group was pretreated with 1 μM for 30 minutes and then added LPS (1 μg / mL) to treat the cells; 9-methyl-3,6-di In the acetylcarbazole group, 3 concentrations were set, and the cells were treated with 5, 10, and 20 μM for 30 minutes, and then LPS (1 μg / mL) was added to treat the cells. After culturing the cells for 6 hours, the cells were collected, centrifuged at 6000 rpm ...

Embodiment 3

[0048] Embodiment 3: detecting the therapeutic effect of compound on asthmatic rat model;

[0049] (1) Take 30 SPF grade male SD rats, weighing about 200g, and divide the rats into 3 groups randomly: normal control group, OVA (ovalbumin)-induced asthma group and 9-methyl-3,6-di Acetylcarbazole-treated group. In the asthma group, 1 mL of OVA (concentration 0.8 g / L) was injected intraperitoneally on the 1st and 8th day, and on the 15th day, an air-compressed nebulizer was used to atomize and challenge with 1% OVA physiological saline solution in a closed plexiglass container. , 30 minutes each time, 3 times a week for 5 weeks. The normal control group was treated with normal saline instead of OVA, and the treatment method was the same. On the basis of the asthma group, the 9-methyl-3,6-diacetylcarbazole treatment group was administered intraperitoneally at a concentration of 20 mg / kg half an hour before the nebulization of 1% OVA normal saline solution.

[0050] (2) Preparati...

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 applications of 9-methyl-3,6-diacetylcarbazole in treating or preventing respiratory inflammatory diseases. The 9-methyl-3,6-diacetylcarbazole is used for the prevention and / oralleviation and / or adjuvant treatment and / or treatment of asthma and chronic obstructive pneumonia. The 9-methyl-3,6-diacetylcarbazole has a significant specific inhibitory effect on PI3Kgamma.

Description

technical field [0001] The invention relates to the technical field of biomedicine, in particular to a specific inhibitor of PI3Kγ, which has the effect of treating respiratory inflammatory diseases such as asthma and chronic obstructive pulmonary disease. Background technique [0002] PI3Ks are a class of lipases that catalyze the phosphorylation of the inositol ring of phosphoinositides and transduce signals as second messengers. PI3K is a complex large family, which can be divided into types I, II, and III according to its structure and substrate specificity. At present, the most widely studied type I PI3K protein receives signals from tyrosine kinase-like receptors and G protein-coupled receptors, and converts PI(4,5)P2 into PI(3,4,5)P3, Thereby, PDK1, Akt and other molecules are recruited and phosphorylated, and the activation signal is transmitted downward, thereby affecting the growth, division, proliferation and survival of cells. [0003] Class I PI3Ks are further...

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): A61K31/403A61P11/00A61P11/06A61P29/00
CPCA61K31/403A61P11/00A61P11/06A61P29/00
Inventor 金坚朱景宇陈蕴杨兆琪蔡燕飞
Owner CF PHARMTECH
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