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

A thiazolidinone compound and its application in the preparation of medicines for treating diseases related to iron disorders

A thiazolidinone class, the technology of said thiazolidinone is applied in thiazolidinone derivatives and their application fields, and can solve the problems of hearing impairment, easy to cause infection, liver damage and the like

Active Publication Date: 2016-04-20
SHANDONG UNIV
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Blood transfusion can easily cause infection, hemolysis, iron load, etc.; compounds targeting γ-peptide chain and α-peptide chain can easily cause liver damage, gastrointestinal tract reactions, inhibit bone marrow proliferation, etc.; deferoxamine can cause hearing impairment, etc.

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
  • A thiazolidinone compound and its application in the preparation of medicines for treating diseases related to iron disorders
  • A thiazolidinone compound and its application in the preparation of medicines for treating diseases related to iron disorders
  • A thiazolidinone compound and its application in the preparation of medicines for treating diseases related to iron disorders

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Preparation of 2-(2-chlorophenylimino)-5-(4-hydroxy-3-methoxybenzylidene)-1,3-thiazol-4-one

[0044]

[0045] by HCl:H 2 The ratio of O (1:4) is dubbed hydrochloric acid solution. Weigh 11.4g (150mmol) of ammonium thiocyanate and dissolve it in 50mL of hydrochloric acid solution, add 10.5mL (100mmol) of 3-toluidine, heat to 85°C under stirring conditions, the mixture becomes clear, after 12 hours of reaction, TLC monitors the reaction, After the reaction, the mixture was cooled to room temperature, and a viscous oily liquid appeared, which was extracted with ethyl acetate, and the extract was washed with 10% hydrochloric acid solution, saturated sodium chloride solution, and water successively, and the solvent was evaporated off the extract under reduced pressure to obtain 2-Tolylthiourea.

[0046] Add 996mg (6.0mmol) of 2-tolylthiourea and 2479mg (30mmol) of anhydrous sodium acetate into 20mL of ethanol, add 1.28mL (12mmol) of ethyl chloroacetate under stirring co...

Embodiment 2

[0050] 76#.2-(2-chlorophenyl)-5-(9H-fluorenylbenzylidene)-1,3-thiazol-4-one

[0051] The preparation method is similar to the preparation of the compound of Example 1.

[0052] The product is a yellow powder with a yield of 75.5%; 1 HNMR (400MHz, CDCl 3 )δ(ppm)=8.0(s,1H),7.85(m,2H),7.72(s,1H),7.45(m,9H),4.12(d,2H).C 23 h 15 ClN 2 OS,ESI-MS:m / z403.7(M+1) + .

Embodiment 3

[0054] 78#.2-(2-Chlorophenyl)-5-(4-methylthiobenzylidene)-1,3-thiazol-4-one

[0055] The preparation method is similar to the preparation of the compound of Example 1.

[0056] The product is an orange powder with a yield of 92.6%; 1 HNMR (400MHz, CDCl 3 )δ(ppm)=8.2(s,1H),7.72(s,1H),7.49(d,1H),7.35(m,7H),2.53(s,3H).C 17 h 13 ClN 2 OS 2 ,ESI-MS:m / z360.0(M+1) + .

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 a thiazolidone compound, wherein a chemical structure of the thiazolidone compound is shown in a general form (I). The invention also discloses application of the thiazolidone compound in preparation of a medicine used for treating thalassemia. Experiments prove that the thiazolidone compound can be used for effectively stimulating expression of hepcidin in cells under the condition that concentration is 10mu M, can be still used for effectively inducing expression of hepcidin in liver when being exposed for 6 hours, 24 hours and 48 hours respectively at a dosage of 30mg / kg in animal level and can be also used for effectively reducing level of serum iron, so that the thiazolidone compound can take hepcidin as a target, can be used for reducing iron level in serum, is hopeful to be a potential medicine used for treating and alleviating iron disorder-related diseases and has a broad clinical application prospect and a great economic development value.

Description

technical field [0001] The invention relates to thiazolidinone derivatives and applications thereof, in particular to a novel thiazolidinone compound and its application in the preparation of medicines for treating diseases related to iron disorders; it belongs to the field of medicinal chemistry. Background technique [0002] Iron is an essential trace element for the body, and it is widely involved in the physiological processes of the body, such as electron transfer, DNA replication, DNA repair, etc. In some diseases, such as β-thalassemia, hereditary hemochromatosis, hepatitis C, alcoholic liver disease, renal hyperfunction, etc., are accompanied by high serum iron levels and low hepcidin expression levels symptom. [0003] β-thalassemia is a kind of disease that seriously threatens human health. It has a high incidence in my country, especially in Guangdong, Guangxi, Guizhou, Hainan and other provinces, and frequently occurs in Southeast Asia and countries around the M...

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): C07D277/54A61K31/426A61P7/06
CPCC07D277/54
Inventor 闫兵刘思金刘寅刘静
Owner SHANDONG UNIV
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