Preparation of sutherlandin-5-cis-p-coumarate and its application in the preparation of drugs for treating rheumatoid arthritis

An arthritis and rheumatoid technology, applied in the preparation of Sutherlandin-5-cis-p-coumarate and its application in the preparation of drugs for the treatment of rheumatoid arthritis, can solve the problems of heavy social burden and high treatment cost

Active Publication Date: 2020-11-03
BINZHOU MEDICAL COLLEGE
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The treatment of RA patients requires long-term medication to control the course of the disease and improve symptoms, and the cost of treatment is high and the social burden is heavy
At present, the drugs used clinically to treat RA mainly include non-steroidal anti-inflammatory drugs (NSAIDs), glucocorticoids, disease-modifying antirheumatic drugs, biological agents and herbal preparations, etc., although they have certain However, most of them have strong toxic and side effects, and there is still a big gap between this and the ideal anti-rheumatoid drug that needs to be taken for a long time

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
  • Preparation of sutherlandin-5-cis-p-coumarate and its application in the preparation of drugs for treating rheumatoid arthritis
  • Preparation of sutherlandin-5-cis-p-coumarate and its application in the preparation of drugs for treating rheumatoid arthritis
  • Preparation of sutherlandin-5-cis-p-coumarate and its application in the preparation of drugs for treating rheumatoid arthritis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] The preparation of embodiment 1.Sutherlandin-5-cis-p-coumarate

[0024] Take the medicinal material of pearl plum, crush it into the coarsest powder, add 20 times the amount of 95% ethanol, soak and extract 1 to 3 times, about 10 hours each time, combine the extracts, filter, dealcoholize and concentrate to about 10% ethanol concentration, add samples On the AB-8 type weakly polar macroporous adsorption resin column, first use 20% ethanol solution to elute 5 column volumes to remove impurities, then use 60% ethanol to elute 4 column volumes, collect the 60% ethanol eluted part, Concentrate, refrigerate and crystallize, filter, and dry under reduced pressure to obtain Sutherlandin-5-cis-p-coumarate coarse crystals. Dissolve the crude crystals in methanol to form a supersaturated solution, recrystallize, filter, and dry under reduced pressure to obtain.

Embodiment 2

[0025] The preparation of embodiment 2.Sutherlandin-5-cis-p-coumarate

[0026] Take the pearl plum medicinal material, crush it into the coarsest powder, add 20 times the amount of methanol, soak and extract 1 to 3 times, about 10 hours each time, combine the extracts, filter, dealcoholize and concentrate to an appropriate volume, and replenish water until the alcohol concentration is about 10% , add sample to D-101 non-polar macroporous adsorption resin column, first use 20% methanol solution to elute 5 column volumes to remove impurities, then use 60% methanol to elute 4 column volumes, collect 60% methanol to wash Partially removed, concentrated, refrigerated for crystallization, filtered, and dried under reduced pressure to obtain Sutherlandin-5-cis-p-coumarate coarse crystals. Dissolve the crude crystals in methanol to form a supersaturated solution, recrystallize, filter, and dry under reduced pressure to obtain.

Embodiment 3

[0027] Example 3. Confirmation of the structure of Sutherlandin-5-cis-p-coumarate

[0028] 1. Instruments and materials

[0029] Jasco P-1020 digital polarimeter, Agilent TOF / 6500 high-resolution mass spectrometer, Shimadzu UV-2401 visible-ultraviolet spectrophotometer, NMR is Bruke Avance III 500NMR spectrometer, melting point analyzer is Yanaco MP53 (melting point is not corrected) ). The Sutherlandin-5-cis-p-coumarate sample was prepared according to the steps in Example 1 above.

[0030] 2. Compound structure identification

[0031] Colorless needles (methanol), mp 94-96°C, easily soluble in dimethyl sulfoxide and methanol, slightly soluble in ethyl acetate, acetone, chloroform, water, insoluble in petroleum ether, [α]2D4-12.2(c 0.43, methanol). Positive ion ESI-MS m / z: 422[M+H] + , 444[M+Na] + , 865[2M+Na] + ; Negative ion ESI-MS m / z: 420[M-H] - , 456[M+Cl] - ,841[2M-H] - . Positive ion HR-ESI-MS m / z: found value 444.1263[M+Na] + , the calculated value is 444....

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 relates to a chemical structure and preparing method of the compound sutherlandin-5-cis-p-coumarate and application of the compound to preparation of drugs for treating rheumatoid arthritis. Sutherlandin-5-cis-p-coumarate is a novel compound prepared from the traditional Chinese medicine Sorbaria sorbifolia (L.) A. Brown. through purification by the applicant of the invention. The compound can remarkably suppress the level of PEG2 and NO in serum of adjuvant arthritis rats. The activity of the compound is close to that of tripterygium glycosides of the same dose, and the compound can be used for preparing drugs for treating rheumatoid arthritis. The chemical structure, preparing method and anti-RA activity of the compound are disclosed for the first time, thus having prominent and substantive features.

Description

technical field [0001] The invention relates to the structure and preparation method of Sutherlandin-5-cis-p-coumarate, and the application of Sutherlandin-5-cis-p-coumarate in the preparation of medicines for treating rheumatoid arthritis. Background technique [0002] Rheumatoid arthritis (RA) is a heterogeneous, systemic, autoimmune disease with symmetrical polyarthritis as the main clinical manifestation. Qualitative autoimmune disease. RA is one of the main causes of human incapacity and disability. The average incidence rate in the world is 0.2% to 1.2%, and the prevalence rate in my country is 0.2% to 0.93%. The treatment of RA patients requires long-term medication to control the course of the disease and improve symptoms, and the cost of treatment is high and the social burden is heavy. At present, the drugs used clinically to treat RA mainly include non-steroidal anti-inflammatory drugs (NSAIDs), glucocorticoids, disease-modifying antirheumatic drugs, biological ...

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 Patents(China)
IPC IPC(8): A61K31/7028C07H15/10C07H1/08A61P29/00A61P19/02
CPCA61K9/205A61K9/2059A61K9/4866A61K31/7028C07H1/08C07H15/10
Inventor 曲桂武吴长景荆杰曹奇志孙亚楠郝玉玲于泽秋张丽刘俊杰
Owner BINZHOU MEDICAL COLLEGE
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