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

Synthesis, preparation and application of a fluorescent probe for recognizing cys, gsh and hocl based on molecular logic gates

A fluorescent probe and logic gate technology, applied in the construction of molecular logic gates, the application of GSH and HOCl, the synthesis of multi-recognition fluorescent probes, and the detection of Cys, which can solve the lack of high sensitivity, the exact change is not very clear, etc. problem, to achieve the effect of good selectivity, wide application value and high yield

Active Publication Date: 2021-05-11
ZHENGZHOU UNIV
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the exact changes of HOCl and Cys / GSH under oxidative stress are not well understood due to the lack of highly sensitive, specific and rapid detection methods

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
  • Synthesis, preparation and application of a fluorescent probe for recognizing cys, gsh and hocl based on molecular logic gates
  • Synthesis, preparation and application of a fluorescent probe for recognizing cys, gsh and hocl based on molecular logic gates
  • Synthesis, preparation and application of a fluorescent probe for recognizing cys, gsh and hocl based on molecular logic gates

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0067] Synthesis of fluorescent probe compound NPCC.

[0068] (1) Synthesis of compound 1

[0069] The known compound 10-acetyl-9-hydroxy-2,3,6,7-tetrahydro-1H-pyrano[2,3-f]pyrido[3,2,1-ij]quinoline-11 (5H)-ketone (897 mg, 3 mmol) and benzaldehyde (334 mg, 3.15 mmol) were dissolved in 25 mL of ethanol, 6–9 drops of piperidine were added during stirring, and refluxed for 14 hours. After the reaction was complete, cool to room temperature, filter with suction, wash the filter cake with ice-cold ethanol, and dry in vacuo to obtain compound 1 as a red solid (896.4 mg, yield 77.2%).

[0070] H NMR spectrum determination: 1 H NMR (400 MHz, CDCl 3 , ppm):1.92-1.99 (m, 4H), 2.76-2.85 (m, 4H), 3.29-3.32 (m, 4H),7.42 (m, 4H), 7.70 (m, 2H), 7.94 (d, 1 H, J =15.8 Hz), 8.46 (d, 1 H, J = 15.8 Hz).

[0071] Carbon NMR Spectrum Determination: 13 C NMR (100 MHz, CDCl 3 , ppm): δ = 20.14, 20.25,21.22, 27.48, 49.82, 50.25, 98.06, 103.11, 105.36, 118.70, 122.75, 124.07,128.88, 128.96, 13...

Embodiment 2

[0084] When the probe of the present invention interacts with Cys, GSH and HOCl, the ultraviolet-visible spectrum and the fluorescence emission spectrum change.

[0085] The probe prepared in Example 1 was dissolved in DMSO to prepare a probe master solution with a probe concentration of 1 mM. The test solution was Tris-HCl (10 mM, 1 mM CTAB) buffer solution, and the pH value of the buffer solution was 7.4. Take 30 μL of the probe mother solution and add it to 3 mL of the test solution to obtain the probe mixed solution. The final concentration of the probe in the mixed solution is 10 μmol / L. The UV-visible spectrum and fluorescence spectrum changes of the probes when they interacted with Cys, GSH and HOCl were tested with a UV-visible spectrophotometer and a fluorescence spectrophotometer. From figure 1 It can be seen that after adding Cys (10 μM) or GSH (10 μM), the maximum ultraviolet absorption peak of the probe blue-shifted from 471 nm to 441 nm, and the fluorescence in...

Embodiment 3

[0087] Fluorescence titration experiment of the probe of the present invention recognizing Cys.

[0088] Example 2 Preparation of the probe mother solution 30 μL was added to 3 mL of the test solution, the final concentration of the probe was 10 μmol / L, and different equivalents (0–4 equivalents) of the Cys mother solution were added, such as figure 2 As shown, with the increase of Cys concentration, the fluorescence intensity of the maximum fluorescence emission peak at 514 nm gradually increased, and the detection limit of the probe to recognize Cys was 8.95 nM.

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 synthesis, preparation and application of a fluorescent probe that recognizes Cys, GSH and HOCl based on molecular logic gates belongs to the field of small molecule fluorescent probes and relates to the field of molecular computer technology. The multi-recognition fluorescent probe has the formula (I) The structural formula shown: Formula (I) The novel fluorescent probe based on the molecular logic gate of the present invention to identify Cys, GSH and HOCl is reported for the first time, has the advantages of low detection limit, high sensitivity and good selectivity, and can realize visual detection; The probe raw material of the invention is cheap and easy to obtain, the yield is high and the preparation cost is low, and is suitable for industrial production; GSH and HOCl are used as input signals, and the fluorescence intensities of the maximum fluorescence emission peaks at 514 nm and 412 nm are used as output signals to construct molecular logic gates. This is the first reported fluorescent probe based on molecular logic gates to identify Cys, GSH and HOCl. Limitations imposed by identifying fluorescent probes.

Description

technical field [0001] The invention belongs to the field of small-molecule fluorescent probes, relates to the technical field of molecular computers, and in particular relates to a method for synthesizing a multi-recognition fluorescent probe, a method for constructing a molecular logic gate and its application in detecting Cys, GSH and HOCl. Background technique [0002] The traditional semiconductor silicon material realizes the logic operation through the change of the voltage; the supramolecular chemistry is through the interaction process between the object and the host and the change of the corresponding spectral signal, and the input and output in the logic calculation process one by one. correspond. The logic operation of the fluorescent probe is to identify two or more target molecules through the probe molecules, and the fluorescence changes generated during the identification process. These target molecules are used as input signals, and fluorescence emission is...

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): C07D491/16C09K11/06G01N21/64
Inventor 叶勇牛华伟彭淑新张永茹赵玉芬
Owner ZHENGZHOU 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