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

GRPAKRGDV-The decapeptide, and preparation, activity and application thereof

A technology of -ome-asp-val-the-obzl, -ome-asp, applied in the field of biomedicine, can solve the problems of thrombolytic drug bleeding, re-embolization, reperfusion injury, etc.

Active Publication Date: 2018-02-16
CAPITAL UNIVERSITY OF MEDICAL SCIENCES
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Existing thrombolytic drugs have problems such as bleeding, reembolization, and reperfusion injury, so finding new anti-ischemic stroke drugs has important application value

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
  • GRPAKRGDV-The decapeptide, and preparation, activity and application thereof
  • GRPAKRGDV-The decapeptide, and preparation, activity and application thereof
  • GRPAKRGDV-The decapeptide, and preparation, activity and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] Embodiment 1 prepares Boc-Ala-Lys(Z)-OBzl(1)

[0031] Dissolve 2.08g (11mmol) Boc-Ala in 20mL anhydrous tetrahydrofuran (THF), add 1.35g (10mmol) 1-hydroxybenzotriazole (HOBt) and 2.47g (12mmol) dissolved in anhydrous THF under ice cooling Dicyclohexylcarbonyldiimide (DCC) was stirred for 0.5 hour to obtain reaction solution A. After 30 minutes, 4.07g (10mmol) HCl Lys(Z)-OBzl was dissolved in 15mL THF, and the pH was adjusted to 9 with N-methylmorpholine, then added to the reaction solution A, stirred at room temperature for 12 hours, TLC (Developer CHCl 3 :MeOH=30:1) shows that HCl·Lys(Z)-OBzl disappears. The dicyclohexylurea (DCU) in the reaction solution was removed by filtration, the reaction solution was concentrated to dryness under reduced pressure, the residue was dissolved in 100 mL of ethyl acetate, and the insoluble matter was filtered off. The filtrate was successively washed 3 times with saturated aqueous sodium bicarbonate solution, 3 times with 5% aque...

Embodiment 2

[0032] Example 2 Preparation of HCl Ala-Lys(Z)-OBzl(2)

[0033] Dissolve 2.0g (3.7mmol) Boc-Ala-Lys(Z)-OBzl in a small amount of dry ethyl acetate, add 20mL of 4N hydrogen chloride-ethyl acetate solution under ice-salt bath, react under ice-cooling for 4 hours, TLC (CHCl 3 :MeOH,30:1) shows that the raw material point disappears and the reaction is complete. The reaction solution was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate and concentrated under reduced pressure. This operation was repeated three times to remove free hydrogen chloride, and the residue was washed three times with anhydrous ether to obtain 1.6 g (90%) of the title compound as a colorless powder. ESI-MS(m / z):442[M+H] + .

Embodiment 3

[0034]Embodiment 3 prepares Boc-Pro-Ala-Lys(Z)-OBzl(3)

[0035] Using the method of Example 1, 1.7 g (78%) of the title compound was obtained as a yellowish oil from 731 mg (3.4 mmol) of Boc-Pro and 1.8 g (3.3 mmol) of HCl·Ala-Lys(Z)-OBzl. ESI-MS(m / z):639[M+H] + .

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 Gly-Arg-Pro-Ala-Lys-Arg-Gly-Asp-Val-The decapeptide, and a preparation method and ischemic stroke treatment activity, antithrombotic activity and thrombolytic activity thereof.Thus, the invention discloses an application of the Gly-Arg-Pro-Ala-Lys-Arg-Gly-Asp-Val-The decapeptide in preparation of ischemic stroke treatment, antithrombotic and hemolytic thrombolytic drugs.

Description

technical field [0001] The present invention relates to Gly-Arg-Pro-Ala-Lys-Arg-Gly-Asp-Val-The decapeptide, to its preparation method, to its activity for treating ischemic stroke, antithrombotic activity and thrombolytic activity. Therefore, the present invention relates to its application in the preparation of antithrombotic and thrombolytic drugs for treating ischemic stroke. The invention relates to the field of biomedicine. Background technique [0002] Coronary heart disease, stroke, and vasculitis are very common cardiovascular and cerebrovascular diseases. With the continuous improvement of people's living standards, the incidence of cardiovascular and cerebrovascular diseases is increasing year by year. Risk factors for cardiovascular and cerebrovascular diseases are prevalent, and the prevalence of cardiovascular and cerebrovascular diseases in my country continues to rise. According to statistics, 1 out of every 5 adults suffers from cardiovascular disease. T...

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): C07K7/06C07K1/10C07K1/02A61K38/08A61P7/02A61P9/10
Inventor 赵明彭师奇吴建辉王玉记武丽飞
Owner CAPITAL UNIVERSITY OF MEDICAL SCIENCES
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