Applications of phosphodiesterase type 4 inhibitors in preparation of novel anti-inflammatory drugs

A technology of phosphodiesterase and anti-inflammatory drugs, applied in the field of medicine, can solve problems such as vermilion dilactone that have not been reported

Inactive Publication Date: 2018-10-09
胡艳
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The prior art has not reported the related reports of vermilion dilactone, isof

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 phosphodiesterase type 4 inhibitors in preparation of novel anti-inflammatory drugs
  • Applications of phosphodiesterase type 4 inhibitors in preparation of novel anti-inflammatory drugs
  • Applications of phosphodiesterase type 4 inhibitors in preparation of novel anti-inflammatory drugs

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0017] The following describes the substantive content of the present invention in detail in conjunction with the drawings and embodiments, but does not limit the protection scope of the present invention.

[0018] According to the literature method (Liu Junfeng et al., RP-HPLC determination of phosphodiesterase 4 inhibitory activity of bitter wood alkaloids in vitro, Chinese modern traditional Chinese medicine, 2009 03 issue) determination of vermilion dilactone, isofantrolactone, and Lushan spicein A Inhibition of phosphodiesterase 4 by bidentate spices and Lushan spices C.

[0019] 1. Experimental materials and instruments

[0020] Vermilion Dilactone, Isopredylactone, Lushan Perfume A, Bidentate Perfume and Lushan Perfume C are self-made or purchased, and the purity is not less than 98%. cAMP and the positive drug Rolipram were purchased from Sigma. Lymphocyte separation medium was purchased from Nanjing Jiancheng Biotech. Blood samples were collected from healthy comme...

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

Applications of phosphodiesterase type 4 inhibitors in preparation of novel anti-inflammatory drugs are disclosed. Salviacoccin, isocolumbin, teupernin A and bidentatin are effective phosphodiesterasetype 4 inhibitors, and teupernin C does not have obvious inhibition effect. In the salviacoccin, the isocolumbin, the teupernin A and the bidentatin, the isocolumbin has highest inhibition effect close to that of a positive drug that is rolipram.

Description

technical field [0001] The invention belongs to the field of medicine and relates to the use of known compounds as phosphodiesterase 4 inhibitors, which can be developed into novel anti-inflammatory drugs. Background technique [0002] Phosphodiesterase 4 widely exists in a variety of inflammatory cells and is closely related to a variety of intracellular inflammations. As the only isoenzyme that degrades cyclic AMP, it can be adjusted by adjusting the concentration of phosphodiesterase 4. The concentration level of cyclic AMP in inflammatory cells plays an anti-inflammatory effect. Therefore, phosphodiesterase 4 inhibitors are of great significance for the development of new anti-inflammatory drugs (references: Tang Huifang et al., Research status and future development direction of phosphodiesterase 4 as anti-inflammatory drug target, Journal of China Pharmaceutical University, 2006 Issue 01). [0003] Vermilion dilactone (CAS accession number: 85564-00-7), isofantandrol...

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): A61K31/37A61P29/00
CPCA61K31/37A61P29/00
Inventor 胡艳
Owner 胡艳
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products