Selective detection of h based on bodipy dye-targeted lysosomes 2 The fluorescent probe, preparation and application of s

A fluorescent probe and lysosome technology, applied in the field of fluorescent probes, can solve the problems of short detection fluorescence wavelength and long response time, and achieve the effects of convenient operation, simple synthesis method and obvious detection signal

Active Publication Date: 2021-10-01
上海安能健生物医药科技有限公司
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In the past few years, various identifications of H 2 Although great progress has been made in fluorescent probes for S, most of the developed probes have more or less limitations, such as short detection wavelength (20 min). Wait

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
  • Selective detection of h based on bodipy dye-targeted lysosomes <sub>2</sub> The fluorescent probe, preparation and application of s
  • Selective detection of h based on bodipy dye-targeted lysosomes <sub>2</sub> The fluorescent probe, preparation and application of s
  • Selective detection of h based on bodipy dye-targeted lysosomes <sub>2</sub> The fluorescent probe, preparation and application of s

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] The preparation steps of the probe are as follows:

[0038] (1) Preparation of Compound 1

[0039]

[0040] N 2 Under the protective ice-water bath, add 1.1 equivalents of triphenylphosphine into the tetrahydrofuran solvent to obtain a mixed solvent, dissolve 2-morpholine ethanol and p-hydroxybenzaldehyde in the mixed solvent according to the equivalent ratio of 1:1.2, and then add 1.1 An equivalent amount of diisopropyl azodicarboxylate was reacted at room temperature for 15 h, the solvent was removed under reduced pressure, and compound 1 was obtained by column chromatography;

[0041] 1 H NMR (400 MHz, CDCl 3 ) δ 9.77 (s, 1H), 7.72 (d, J = 8.7 Hz, 2H), 6.92(d, J= 8.7 Hz, 2H), 4.10 (t, J = 5.7 Hz, 2H), 3.69 – 3.54 (m, 4H), 2.73 (t, J = 5.7 Hz, 2H), 2.54 – 2.40 (m, 4H).

[0042] (2) Preparation of compound 2

[0043]

[0044] Dissolve compound 1 in tetrahydrofuran, add 2.2 equivalents of 2,4-dimethylpyrrole, add 0.2 mL of trifluoroacetic acid, react a...

Embodiment 2

[0055] The preparation steps of the probe are as follows:

[0056] (1) Preparation of compound 1

[0057] N 2 Under the protected ice-water bath, add 1 equivalent of triphenylphosphine into the tetrahydrofuran solvent to obtain a mixed solvent, dissolve 2-morpholine ethanol and p-hydroxybenzaldehyde in the mixed solvent according to the equivalent ratio of 1:1, and then add 1.5 An equivalent amount of diisopropyl azodicarboxylate was reacted at room temperature for 12 h, the solvent was removed under reduced pressure, and compound 1 was obtained by column chromatography;

[0058] (2) Preparation of Compound 2

[0059] Dissolve compound 1 in tetrahydrofuran, add 2 equivalents of 2,4-dimethylpyrrole, add 0.1 mL trifluoroacetic acid, react at room temperature for 15 h, then add 1.5 equivalents of tetrachlorobenzoquinone, react at room temperature for 0.5 h, follow Add triethylamine and boron trifluoride diethyl ether in a ratio of 5:8 equivalent, react at room temperature for ...

Embodiment 3

[0065] The preparation steps of the probe are as follows:

[0066] (1) Preparation of compound 1

[0067] N 2 Under the protective ice-water bath, 1.5 equivalents of triphenylphosphine was added to the tetrahydrofuran solvent to obtain a mixed solvent, and 2-morpholine ethanol and p-hydroxybenzaldehyde were dissolved in the mixed solvent according to the equivalent ratio of 1:1.5, and then 1 An equivalent amount of diisopropyl azodicarboxylate was reacted at room temperature for 18 h, the solvent was removed under reduced pressure, and compound 1 was obtained by column chromatography;

[0068] (2) Preparation of Compound 2

[0069] Dissolve compound 1 in tetrahydrofuran, add 3 equivalents of 2,4-dimethylpyrrole, add 0.2 mL of trifluoroacetic acid, react at room temperature for 12 h, then add 1.1 equivalent of tetrachlorobenzoquinone, react at room temperature for 0.8 h, follow Add triethylamine and boron trifluoride diethyl ether at a ratio of 7:9, react at room temperature...

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 provides a BODIPY-based fluorescent dye targeting lysosomes selectively responding to H 2 The fluorescent probe, preparation and application of S, the probe uses BODIPY dye as the fluorophore, and 2,4-dinitrobenzenesulfonyl as the recognition group. The sensing mechanism is based on the H 2 S induces the cleavage of the 2,4‑dinitrobenzenesulfonyl group in the probe, thereby inhibiting the process of photoinduced electron transfer (PET), resulting in the restoration of probe fluorescence. The above probes were detected by UV and fluorescence spectrometers for H 2 S is free from interference from other amino acids, active sulfides, and representative anions. The detection process is simple, rapid, and sensitive, with a detection limit of 4.75 nM. More importantly, the probe can target lysosomes and simultaneously detect H in cells 2 S, has a good application prospect in the field of biological monitoring.

Description

technical field [0001] The invention relates to the field of fluorescent probes, in particular to a BODIPY-based fluorescent dye targeting lysosomes selectively responding to H 2 S fluorescent probe, preparation and application. Background technique [0002] Hydrogen sulfide (H 2 S) has received great attention from researchers because it is considered to be the third important gas signal molecule after carbon monoxide (CO) and nitric oxide (NO) in the living system. In recent years, increasing research results have shown that endogenously produced hydrogen sulfide plays an important role in a wide range of physiological and pathological processes. On the other hand, H 2 Abnormal S content is closely related to many serious diseases, such as Alzheimer's disease, Down syndrome, diabetes and liver cirrhosis, etc. Despite these findings, H 2 The underlying molecular properties of S remain unclear. Cell lysosome is an important dynamic subcellular organelle, which is respon...

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): C07F5/02C09K11/06G01N21/64
CPCC07F5/022C09K11/06C09K2211/1014C09K2211/1033C09K2211/1055G01N21/6428G01N21/6458G01N21/6486
Inventor 王佳敏张健岳金磊陶远芳王瀚王楠楠苏慧慧赵伟利
Owner 上海安能健生物医药科技有限公司
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