Use of a polyacetylenic compound for reducing uric acid

A compound and uric acid-lowering technology, applied in the field of pharmaceuticals, can solve the problems of weak xanthine oxidase inhibitory effect and inability to lower uric acid gout, etc., and achieve a significant effect of lowering uric acid

Active Publication Date: 2022-01-11
CATCH BIO SCI & TECH
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Although there are bibliographical reports in the prior art: some chain polyalkyne compounds have certain inhibitory effect to xanthine oxidase (XO) in vitro, yet cause it to xanthine oxidase (XO) in vivo because of its easy metabolism in vivo. XO) has weak inhibitory effect, so it cannot be used as a potential drug for lowering uric acid or treating gout

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
  • Use of a polyacetylenic compound for reducing uric acid
  • Use of a polyacetylenic compound for reducing uric acid
  • Use of a polyacetylenic compound for reducing uric acid

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0065] Example 1 Preparation of Compound 1-6

[0066]

[0067] The specific operation steps are as follows:

[0068] Take 100 kg of herb decoction pieces, add 10 times the volume of 70% ethanol aqueous solution to extract 3 times at 80°C, extract for 1.5 hours each time, filter to remove the medicinal residue, and concentrate under reduced pressure to 100L, wherein the solid content is about 15kg, to obtain concentrated solution A .

[0069] The concentrated solution A was separated by a low-pressure D101 column (column diameter 28cm×height 162cm, column volume 100L), and was eluted with an ethanol-water gradient (first eluted 4BV with 30% ethanol-water solution, then eluted 4BV with 95% ethanol-water solution ), collect the eluate of 95% ethanol aqueous solution and concentrate to a solid content of about 3kg to obtain concentrate B.

[0070] The concentrated solution B was separated by LX-20SS column (column diameter 20cm×height 78cm, column volume 25L), and ethanol aq...

Embodiment 2

[0076] Example 2 Preparation of Compound 7-12

[0077]

[0078]

[0079] The synthetic route is as follows:

[0080]

[0081] The reaction conditions are as follows:

[0082] a: SeO 2 , 1,4-dioxane, 90°C;

[0083] b: (1) Ag 2 O,H 2 O / NaOH (40%), 0°C; (2) HCl (36%), pH=5, r.t.;

[0084] c: Benzoic acid, DCC, DMAP, CH 2 Cl 2 , r.t.;

[0085] d: 4-methylbenzoic acid, DCC, DMAP, CH 2 Cl 2 , r.t.;

[0086] e: HCHO, AlCl 3 , HCl, CH 2 Cl 2 ;

[0087] f:CH 3 COOCH 3 , HCl / AcOH (10%), r.t..

[0088] The specific operation steps are as follows:

[0089] Take 10g atractylodes and dissolve in 30mL 1,4-dioxane, add 0.6g SeO to the solution 2 , stirred and reacted at 90°C for 8 hours, then filtered the reaction solution through a 45 μM microporous filter, and then performed silica gel column chromatography with petroleum ether-ethyl acetate at a volume ratio of 20:1 to 5:1 as the mobile phase. After separation and purification, 0.6 g of the compound (yield 6%...

Embodiment 3

[0095] Example 3 Preparation of Compound 13

[0096]

[0097] The synthetic route is as follows:

[0098]

[0099] The specific operation steps are as follows:

[0100] Under nitrogen protection, will contain 2.0mol 1-bromo-2-styrene, 0.02mol PdCl 2 (PPh 3 ) 2 , 0.04mol CuI and 1.5mol Et 3 The 0.2 mol / L THF solution of N was stirred rapidly, and the 0.2 mol / L THF solution containing 1.0 mol 1,4-bis(trimethylsilyl)-1,3-butadiyne was added at room temperature. After reacting for 1 hour, with 100 mL of saturated NH 4 The reaction was quenched with aqueous Cl solution, and then extracted with 3*50 mL ethyl acetate to obtain an ethyl acetate organic layer extract. The ethyl acetate organic layer extract was washed with 50 mL of saturated NaCl aqueous solution, and then washed with Na2SO 4 Dry and concentrate in vacuo to obtain a concentrated solution. The concentrated solution is separated and purified by silica gel column chromatography with petroleum ether-ethyl a...

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 belongs to the field of medicines, and in particular relates to the use of polyacetylenic compounds for reducing uric acid. The polyalkyne compound has a structure shown in formula (I): R 1 and R 2 As shown in the definition of the description of the present invention. The present invention finds through the animal model of hyperuricemia that the polyalkyne compound of the present invention has significant uric acid-lowering effect in vivo, and can be used as a potential uric acid-lowering or gout-treating drug.

Description

technical field [0001] The invention belongs to the field of medicines, and in particular relates to the use of polyacetylenic compounds for reducing uric acid. Background technique [0002] Uric acid is the final metabolite of human purine compounds, and purine metabolism disorders lead to hyperuricemia. Under a normal purine diet, if the blood uric acid level on an empty stomach is higher than 416 μmol / L for men and 360 μmol / L for women on two different days, it is called hyperuricemia. Gout is a crystal-associated arthropathy caused by the deposition of monosodium urate (MSU), which is directly related to hyperuricemia caused by purine metabolic disorders and / or decreased uric acid excretion. The main clinical manifestation is hyperuricemia , recurrent gouty acute arthritis, gouty chronic arthritis and tophi, gouty nephropathy and renal uric acid stones, etc. In severe cases, joint disability and renal insufficiency may occur. In addition, gout is often accompanied by d...

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): A61K31/341A61K31/216A61K31/22A61K31/7028A61K31/201A61K31/015A61P19/06
Inventor 温尧林
Owner CATCH BIO SCI & TECH
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap