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

5-benzylidene-2-phenyl thiazolone compound as well as preparation and application thereof

A technology of phenylthiazolone and benzylidene, which is applied in the fields of medicinal chemistry and pharmacotherapeutics, can solve problems such as genome instability and cell cycle arrest, and achieves simple and easy preparation method, easily available raw materials, and strong tumor cells. Effect of proliferation inhibitory activity

Active Publication Date: 2018-10-23
UNIV OF JINAN
View PDF8 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Misregulation of these histone demethylases often causes cell cycle arrest and may also lead to genomic instability in cancer

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
  • 5-benzylidene-2-phenyl thiazolone compound as well as preparation and application thereof
  • 5-benzylidene-2-phenyl thiazolone compound as well as preparation and application thereof
  • 5-benzylidene-2-phenyl thiazolone compound as well as preparation and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] The preparation of embodiment 1 general formula (I) compound

[0039] Dissolve p-toluonitrile (59 mg, 0.5 mmol), thioglycolic acid (1 equiv), triethylamine (1 equiv) and the corresponding benzaldehyde derivative (1 equiv) in 10 mL of ethanol. The mixture was heated to reflux for 12 hours, and then the solvent was removed under reduced pressure, and the residue was separated by column chromatography to obtain the target compound.

[0040]

[0041] The following products are obtained:

[0042] ( Z )-5-benzylidene-2-( p -Methylphenyl)thiazole-4(5 H )-ketone (I-1), yellow solid (46 mg, 33%), melting point 190-192 °C. 1 H NMR (600 MHz, CDCl 3 ) δ 8.12 (d, J= 7.8 Hz, 2H), 8.05 (s, 1H),7.68 (d, J = 8.4 Hz, 2H), 7.50 (d, J = 8.4 Hz, 2H), 7.37 (d, J = 7.8 Hz, 2H),2.48 (s, 3H). 13 C NMR (150 MHz, CDCl 3 ) δ 187.1, 183.4, 146.7, 138.1, 133.9, 131.0, 130.6, 130.0, 129.2, 129.2, 129.0, 126.6, 22.0. ESI-MS m / z : 280.0 [M+H] + .

[0043] ( Z )-5-(2-Methoxybenzyli...

Embodiment 2

[0068] Example 2 The enzyme activity inhibitory activity of compounds was tested by radioisotope method.

[0069] 1. Prepare 1x assay buffer (improved Tris-HCl buffer); 2. Dilute the compound to the desired concentration in a 96-well plate; 3. Prepare protein solution, also use 1x assay buffer; 4. Dilute the substrate Add to 1x assay buffer to prepare substrate solution; 5. [ 3 H]-SAM was added to 1x assay buffer to prepare [ 3 H]-SAM solution; 6. Add SAM to 1x assay buffer to prepare a cold SAM solution; 7. Pipette 10 μL protein solution to a 96-well plate containing the compound; 8. Incubate at room temperature for 15 minutes; 9. Add 10 μL substrate solution to each well; 10. Add 10 μL [ 3 H]-SAM solution initiates the reaction; 11. Incubate at room temperature for 240 minutes. 12. Add 10 μL of cold SAM solution to each well to terminate the reaction; 13. Transfer 40 μL of the reaction mixture solution to the GF / B plate, and wash with triple-distilled water for 3 times in...

Embodiment 3

[0084] Example 3 Effects of Compounds on Cell Proliferation

[0085] 1. Test method

[0086] (1) Cell culture

[0087] The culture medium used for MV4-11, Jeko, KOPN8, RCH-ACV, REH, RS4.11, THP1, U937, NALM6 cell culture is RPMI 1640 + 10% fetal bovine serum, and in order to prevent bacterial contamination, 100 U / mL penicillin and 100 μg / mL streptomycin. The cells were cultured at 37°C and 5% CO2 saturated humidity, and the cells used in the experiment were all in the logarithmic growth phase.

[0088] (2) Detection of cell proliferation activity

[0089] Adjust cell concentration to 1 x 10 5 / mL and inoculated in a 24-well culture plate with a volume of 1 mL per well. Set up a control group and an experimental group. The control group was added with DMSO, and the experimental group was added with a small molecule inhibitor of PRMT5 activity to a final concentration of 0-100 μM. Three detection time points were set for MV4-11 cells, which were 4, 8 and 12 days respectiv...

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 5-benzylidene-2-phenyl thiazolone compound as well as preparation and application thereof. In particular, the compound provided by the invention has a structure shown as a general formula (I), wherein the definitions of each group and substituent are described in the description. The invention further discloses a preparation method of the compound and application of thecompound to the prevention and / or treatment of cancer-related diseases. The compound provided by the invention has superior inhibitory activity on protein-arginine methyltransferases 1 (PRMT1), protein-arginine methyltransferases 5 (PRMT5) and histone demethylase LSD1, and can induce tumor cell apoptosis and retard tumor cells at a G1 stage, so that the compound can be used for preparing a seriesof medicaments for treating diseases related to abnormal activities of the PRMT1, the PRMT5 and the histone demethylase LSD1. The general formula (I) is shown in the description.

Description

technical field [0001] The present invention relates to the fields of medicinal chemistry and pharmacotherapeutics, in particular to the preparation and application of a 5-benzylidene-2-phenylthiazolone compound represented by formula I. Background technique [0002] Methylation of histone lysines and arginines is one of the more well-studied post-translational modifications. Its methylation status is balanced by two classes of enzymes: histone methyltransferases (HMTs) and histone demethylases (HDMs). And its abnormal state is associated with many human diseases. [0003] Arginine methylation involved in the protein arginine methyltransferase (PRMTs) family is a post-translational modification widely present in the nucleus and cytoplasm, which uses S-adenosyl-methionine as the methyl donor In the body, the nitrogen atom of the arginine side chain of the protein is methylated to generate S-adenosyl homocysteine ​​and methyl arginine. The substrates of PRMTs are proteins r...

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): C07D277/34A61K31/426A61P35/00A61P35/02
CPCA61P35/00A61P35/02C07D277/34
Inventor 朱孔凯江成世张华宋佳丽陶洪瑞
Owner UNIV OF JINAN
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