CN103936724A - Fluorescent probe for detecting histidine and precursors and preparation method of fluorescent probe - Google Patents
Fluorescent probe for detecting histidine and precursors and preparation method of fluorescent probe Download PDFInfo
- Publication number
- CN103936724A CN103936724A CN201410139352.5A CN201410139352A CN103936724A CN 103936724 A CN103936724 A CN 103936724A CN 201410139352 A CN201410139352 A CN 201410139352A CN 103936724 A CN103936724 A CN 103936724A
- Authority
- CN
- China
- Prior art keywords
- fluorescent probe
- histidine
- compound
- precursors
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Abstract
The invention relates to a fluorescent probe for detecting histidine and precursors of the fluorescent probe as well as preparation method of the fluorescent probe. According to the invention, two precursors of the fluorescent probe are prepared by respectively adopting naphthalimides or umbelliferone as fluorophore, and then the two precursors respectively complex with metal to obtain the fluorescent probe which can be used for detecting histidine. After being combined with the histidine, the fluorescence of the fluorescent probe Ia at 476nm is enhanced slightly, and the fluorescence at 537nm is enhanced obviously; and the fluorescence of the fluorescent probe IIb at 454nm is enhanced obviously. In addition, the fluorescent probe provided by the invention also has the advantages that (1) the fluorescent probe has good water solubility and can be applicable to the histidine detection for a biological system; (2) the fluorescent probe is high in stability, can be used after long-term storage, and is applicable to various environmental systems such as neutral, weak acid and weak alkaline environmental systems; (3) the fluorescent probe is high in sensitivity and anti-interference (little interference is generated in reaction with other amino acids), and the like.
Description
The application is application number: 201110355596.3, and the applying date: on November 11st, 2011, denomination of invention: the fluorescent probe of test set propylhomoserin and presoma thereof and their preparation method's divisional application.
Technical field
The present invention relates to a kind of fluorescent probe for detection of Histidine and presoma thereof and their preparation method.
Background technology
Histidine is one of amino acid in basic 20, and for baby and children, Histidine is the indispensable amino acid of human body, and after growing for many years, human body just can oneself synthesize.Histidine is vital in the physiological activity of human body.Imidazole ring on Histidine side chain is the binding site of many metalloprotein, and still some specify catalytic center [Chen, the G.N. of enzymes simultaneously; Wu, X.P.; Duan, J.P.; Chen, H.Q.Talanta1999 (49): 319 – 330].Histidine can keep organic eubolism, and neuroprotective cell passes to body parts by information from brain.But Histidine content in vivo must maintain in certain scope, the Histidine of abnormal level is the tendency of some diseases normally, for example chronic kidney diseases [Am.J.Clin.Nutr.2008 (87): 1860 – 1866], acute hepatic failure [Am.J.Pathol., 2010 (176): 1400-1408], rheumatoid arthritis [J.Clin.Invest., 1975 (55): 1164-1173] etc.Therefore researching and developing Histidine detection method is necessary.
The detection method of Histidine has a lot, comprises cyclic voltammetry, ultraviolet-visible spectrophotometry, fluorometry, utilizes in addition metal luminous etc.In these reported testing method, due to fluorometry high sensitivity, simplicity and economy, be more and more subject to people's concern and attention.
Czarnik seminar has just proposed fluorescence sense as far back as nineteen ninety-five and has detected amino acid whose importance and urgency [Chem.Biol.1995 (2): 423-428].In coming years, a series of fluorescent probe for detection of Histidine [J.Chem.Soc., Chem.Commun., 1995,2439 have been synthesized in the design of many seminar; Chem.Commun.1997,581-582; J.Am.Chem.Soc.2005 (127): 3362-3365 etc.].But these probes are due to synthetic more difficult, or because quantum yield is low, the inferior position such as fluorescent emission wavelength is short, has limited the widespread use of these probes.Therefore, the present invention mainly wishes by simple synthesis step, design novel, the relatively long or high fluorescent probe of quantum yield of wavelength.
Summary of the invention
One of object of the present invention is, a kind of presoma for the preparation of test set propylhomoserin fluorescent probe is provided;
Two of object of the present invention is, a kind of fluorescent probe of test set propylhomoserin is provided;
Three of object of the present invention is, a kind of method of preparing above-mentioned presoma and fluorescent probe is provided.
Presoma for the preparation of test set propylhomoserin fluorescent probe provided by the present invention, it is the compound shown in formula I or formula II:
In formula, Boc is tertbutyloxycarbonyl.
The fluorescent probe of test set propylhomoserin provided by the present invention, it is the compound shown in formula Ia or formula IIb:
It is fluorophore that the present invention adopts respectively naphthalimide or umbelliferone, has prepared the presoma of two kinds of fluorescent probes, more respectively can be for detection of the fluorescent probe of Histidine with metal complex acquisition.After in conjunction with Histidine, fluorescent probe Ia slightly strengthens at the fluorescence at 476nm place, and the fluorescence at 537nm place has obvious enhancing; And fluorescent probe IIb obviously strengthens at the fluorescence at 454nm place.In addition, fluorescent probe provided by the present invention also tool have the following advantages:
(1) have good water-solublely, the Histidine that can be applicable to living things system detects;
(2) stability is high, can preserve for a long time use, is applicable to the multiple environmental systems such as neutrality, slightly acidic and weakly alkaline;
(3) there is very high sensitivity, and anti-interference (very little with the interference that other amino acid effect produces).
Brief description of the drawings
Fig. 1 is the Ultraluminescence spectrogram of compound shown in formula Ia;
Fig. 2 is the Ultraluminescence spectrogram of compound shown in formula IIb;
Fig. 3 is the fluorescence spectrum figure of fluorescent probe provided by the invention under different pH condition;
Wherein: chemical combination shown in (a)-formula Ia, compound shown in (b)-formula IIb.
Fig. 4 is the fluorescence response curve that fluorescent probe provided by the invention detects Histidine;
Wherein: chemical combination shown in (a)-formula Ia, compound shown in (b)-formula IIb.
Fig. 5 is the fluorescence response histogram of fluorescent probe provided by the invention to different aminoacids;
Wherein: chemical combination shown in (a)-formula Ia, compound shown in (b)-formula IIb.
Embodiment
The present invention also provides a kind of method of preparing described presoma and fluorescent probe, and its key step is:
With the bromo-5-of 4-nitro-1,8-naphthalene dicarboxylic anhydride is raw material, reacts with n-Butyl Amine 99, obtains intermediate A 1; Intermediate A 1 and N-tertbutyloxycarbonyl-reacting ethylenediamine, obtain intermediate A 2; Intermediate A 2 is reacted with 2-aminomethyl-pyridine, obtains the compound shown in formula I (presoma); Compound shown in formula I reacts with mantoquita, obtains fluorescent probe (compound shown in formula Ia); Or,
Taking umbelliferone as raw material, with vinegar (acid) anhydride reactant, obtain intermediate B 1; Intermediate B 1 is reacted with trifluoroacetic acid, obtains intermediate B 2; Intermediate B 2 with the compound (presoma) shown in formula II; Compound shown in formula II reacts with nickel salt, obtains fluorescent probe (compound shown in formula IIb).
Described preparation
Below by specific embodiment, the invention will be further described.In the room temperature described in the following example be: 20 DEG C～25 DEG C, described column chromatography all adopts silicagel column.
Embodiment 1.
The preparation of compound shown in formula Ia
(1) compd A 1 is synthetic
By bromo-4-5-nitro-1,8-naphthalene dicarboxylic anhydride 0.5g(1.6mmol) be dissolved in 20ml ethanol, stir.Add 0.096g n-Butyl Amine 99 (1.6mmol), reflux three hours, TCL point plate is followed the tracks of, to raw material point disappearance or no longer to subtract when light be reaction end.Cooling, filter, then use ethyl alcohol recrystallization, obtain brown solid.Fusing point: 175.8-176.2 DEG C.Yield: 77.8%.
1H?NMR(400MHz,CDCl
3,20℃):δ8.71(d,J=7.6Hz,1H),8.52(d,J=8.0Hz,1H),8.22(d,J=8.0Hz,1H),7.94(d,J=8.0Hz,1H),4.18(t,J=7.6Hz,2H),1.76–1.68(m,2H),1.50–1.41(m,2H),0.99(t,J=7.2Hz,3H).
13C?NMR(100MHz,CDCl
3,20℃):δ162.79,162.02,151.25,135.96,132.32,131.20,130.52,125.77,124.07,123.54,122.48,121.19,40.74,30.02,20.31,13.79.
(2) compd A 2 is synthetic
1.0g (2.6mmol) compd A 1 is dissolved in to the DMF of 5mL, slowly adds the N-Boc-quadrol of 424.7mg under room temperature, continue stirring at room temperature 6 hours, it is complete that TLC tracks to raw material primitive reaction.Stopped reaction, removal of solvent under reduced pressure, column chromatography for separation (developping agent: methylene dichloride), obtains faint yellow solid, productive rate 76.1%.
1H?NMR(400MHz,CDCl
3,20℃):δ8.37(d,J=8.4Hz,1H),8.23(d,J=8.0Hz,1H),7.72(d,J=8.0Hz,1H),7.28(s,1H),6.67(d,J=8.4Hz,1H),5.13(s,1H),4.12(dd,J=7.2Hz,7.6Hz,2H),3.61(s,2H),3.49(s,2H),1.73–1.65(m,2H),1.48–1.40(m,12H),0.97(t,J=7.2Hz,3H).
13C?NMR(100MHz,CDCl
3,20℃):δ163.97,163.50,156.10,150.15,134.72,132.24,131.84,131.05,124.59,122.45,117.57,110.16,105.83,79.95,43.75,40.11,39.16,30.17,28.45,20.42,13.88.
(3) Compound I is synthetic
0.5g (1.0mmol) compd A 2 and 330mg (3.0mmol) 2-aminomethyl-pyridine are placed in to the ethylene glycol monomethyl ether of 10mL, are heated to reflux, reaction is spent the night, and it is complete that TLC tracks to raw material primitive reaction.Removal of solvent under reduced pressure, column chromatography for separation (methylene dichloride: methyl alcohol=100: 1(v/v)), obtain faint yellow solid, productive rate 40.2%.
1H?NMR(400MHz,CDCl
3,20℃):δ8.55(d,J=7.2Hz,1H),8.41(d,J=8.4Hz,1H),8.26(dd,J=9.2Hz,9.2Hz,1H),7.76(d,J=8.0Hz,1H),7.69(s,1H),7,59(dd,J=8.0Hz,7.6Hz,1H),7.06(s,1H),6.71(d,J=8.8Hz,1H),6.54(d,J=8.4Hz,1H),5.26(s,1H),4.18–4.11(m,2H),3.64(t,J=4.0Hz,15.2Hz,2H),3.48(dd,J=4.8Hz,17.6Hz,2H),1.43(t,J=6.4Hz,2H),1.48–1.44(m,12H),0.97(t,J=7.2Hz,3H).
13C?NMR(100MHz,CDCl
3,20℃):δ164.81,164.26,158.62,150.11,134,81,134.53,132.35,131.88,131.09,129.74,127.00,124.65,122.83,120.31,109.86,105.86,103.26,80.71,46.76,43.79,40.11,39.96,39.47,30.34,28.43,28.37,20.46,13.93.
HREI (ES
+): C
29h
36n
5o
4(M+H
+), calculated value: 518.2767; Observed value: 518.2761.
(4) preparation of target compound (Ia)
Compound I is dissolved in to anhydrous methanol, then adds the Cu (ClO of 1.0equiv
4)
2, stirring at room temperature 1 hour, methyl alcohol is removed in decompression, obtains Compound I a.
Embodiment 2
The preparation of compound shown in formula IIb
(1) compound B-11 is synthetic
In the round-bottomed flask of 100mL, umbelliferone (3.1g, 19.1mmol) is joined to 50mL methylene dichloride, form suspension liquid, then add 2mL acetic anhydride and a pyridine.Above-mentioned reaction solution stirred overnight at room temperature is obtained to flaxen settled solution.Methylene chloride decompression is spin-dried for, obtains flaxen crude product solid.Joined in 100mL water again, be extracted with ethyl acetate, get organic layer, water layer discarded, removes ethyl acetate after anhydrous sodium sulfate drying by Rotary Evaporators, obtains flaxen solid.The separation of employing column chromatography chromatogram (sherwood oil: ethyl acetate=2: 1, (v/v)), obtain 3.8g(productive rate 97%) white solid.
1H?NMR(400MHz,CDCl
3):δ7.71(d,1H,J=4.8Hz),7.51(d,J=4.2Hz,1H),7.14(d,J=1Hz,1H),7.07(dd,J=3.1Hz,5.5Hz,1H),6.42(d,J=4.8Hz,1H),2.36(s,3H).
(2) compd B 2 is synthetic
Under the condition of ice bath, in the round-bottomed flask of 50mL, add 10mL trifluoroacetic acid, compound B-11 (1.5g, 7.4mmol) and urotropine (1.5g, 10.7mmol).Add recession deicing and bathe, question response liquid temp rises to after room temperature, reheats and refluxes 8 hours.TLC follows the tracks of reaction, after question response finishes, excessive trifluoroacetic acid decompression is spin-dried for and obtains orange-yellow viscous liquid, adds 30mL water, under the condition of 60 DEG C, stirs after 30 minutes again, is placed in the middle of ice bath, separates out immediately flaxen solid.By reaction solution suction filtration, collect faint yellow solid, water is washed several times more.As washing and dehydrating integrated machine, adopt column chromatography chromatogram separating-purifying (developping agent: methylene dichloride) with methylene dichloride, obtain faint yellow solid (0.76g, productive rate 53%).
1H?NMR（400MHz,CDCl
3）：δ12.22(s,1H),10.61(s,1H),7.67(d,J=4.8Hz,1H),7.61(d,J=4.4Hz,1H),7.28(s,1H),6.9(d,J=4.4Hz,1H),6.34(d,J=4.8Hz,1H).
13C?NMR(100MHz,CDCl
3):δ108.69,110.87,113.42,114.70,136.01,143.37,156.76,159.10,165.50,192.93.
(3) Compound I I's is synthetic
In 25mL round-bottomed flask, add Histidine methyl ester hydrochloride (580mg, 2.4mmol), add anhydrous methanol make its dissolve, then drip 500mg(4.9mmol) triethylamine, at once with regard to adularescent Precipitation (triethylamine hydrochloride).Under the condition of argon shield, by reaction solution stirring at room temperature 30 minutes until Histidine methyl ester hydrochloride complete reaction generates Histidine methyl esters.Suction filtration is removed triethylamine hydrochloride; again methyl alcohol decompression is spin-dried for; obtain white solid; directly Histidine methyl esters is joined and is dissolved with B2(380mg; in dry ethanol solution 2mmol); under agitation; the very fast yellowing of ethanol solution; follow the tracks of reaction until B2 reacts completely by a plate; in reaction solution, add triacetyl sodium borohydride (510mg, 2.4mmol) again, reaction solution color is become faint yellow gradually by yellow; continue stirring reaction 2 hours, find to have generated the material of hyperfluorescenceZeng Yongminggaoyingguang by a plate.By the time, after having reacted, ethanol decompression is spin-dried for, the separation of employing column chromatography chromatogram post (methylene dichloride: methyl alcohol=15: 1, (v/v)), lurid transparent solid (550mg, productive rate 80%) obtained.
1H?NMR(400MHz,CD3OD):δ7.83(d,J=4.6Hz,1H),7.57(s,1H),7.38(d,J=4.2Hz,1H),6.87(s,1H),6.75(d,J=4.4Hz,1H),6.18(d,J=4.8Hz,1H),4.10(dd,J=6.6Hz,20.6Hz,2H),3.67(s,3H),3.37(s,1H),2.93-2.87(m,2H);
13C?NMR(100MHz,CDCl
3):δ173.78,161.85,161.46,153.39,145.01,135.07,128.12,112.92,111.51,110.74,110.52,59.92,51.072,40.23,29.95.
HRMS (ES
+) calculated value, 344.1246; Observed value, 344.1238.
(4) target compound (IIb)
Compound I I is dissolved in to anhydrous methanol, then adds the Ni (ClO of 1.0equiv
4)
2, stirring at room temperature 1 hour, methyl alcohol is removed in decompression, obtains Compound I Ib.
Embodiment 3
The ultraviolet of Compound I a and IIb, fluorescence spectrum character
Compound I a and Compound I Ib are configured to 10
-3the DMSO mother liquor of mol/L, then respectively with corresponding buffered soln dilution 10
-5the test fluid of mol/L concentration, then adds the metal ion of different concns, uv-absorbing and the fluorescent emission of test metal complex.As shown in Figure 1 and Figure 2, Compound I is at complexing metal Cu
2+after, maximal ultraviolet absorption is at 460nm, and maximum fluorescence emission is 472nm; Compound I I is at complexing metal Ni
2+after, maximal ultraviolet absorption is at 350nm, and maximum fluorescence emission is at 454nm.
Embodiment 4
Compound I a and Compound I Ib are at the change in fluorescence curve of different pH condition
Compound I a and Compound I Ib are diluted to 10 with corresponding ethanol-water system and aqueous systems
-5mol/L, then, respectively by the pH value of perchloric acid and sodium hydroxide solution regulation system, records the fluorescent emission curve under condition of different pH, and it the results are shown in Figure 3.
Embodiment 5
Compound I a and the response of Compound I Ib to Histidine
By Compound I a and for Compound I Ib corresponding buffer system (Ia is dissolved in ethanol/water, 40/60, v/v, 50mM HEPES, pH=7.2; IIb is dissolved in MOPS(50mM, containing 10mM NaCl, pH=7.2)) be diluted to 10
-5mol/L, adds the Histidine of different equivalents, measures deblooming change curve, and it the results are shown in Figure 4.
Embodiment 6
Compound I a and Compound I Ib are to other amino acid whose response
By Compound I a and for Compound I Ib corresponding buffer system (Ia is dissolved in ethanol/water, 40/60, v/v, 50mM HEPES, pH=7.2; IIb is dissolved in MOPS(50mM, containing 10mM NaCl, pH=7.2)) be diluted to 10
-5mol/L, adds each seed amino acid of different equivalents, measures deblooming change curve, and it the results are shown in Figure 5.
Claims (3)
1. for the preparation of a presoma for test set propylhomoserin fluorescent probe, it is the compound shown in formula II:
Taking presoma described in claim 1 as part, for detection of a fluorescent probe for Histidine, it is characterized in that, described fluorescent probe is made by the following preparation method of key step:
Taking umbelliferone as raw material, react with aceticanhydride, obtain intermediate B 1; Intermediate B 1 is reacted with trifluoroacetic acid, obtains intermediate B 2; Intermediate B 2 is reacted to obtain the compound shown in formula II with Histidine methyl esters; Compound shown in formula II reacts with nickel salt, obtains target:
3. method as claimed in claim 2, is characterized in that, wherein said nickel salt is Ni (ClO
4)
2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410139352.5A CN103936724B (en) | 2011-11-11 | 2011-11-11 | The fluorescent probe of test set propylhomoserin and presoma thereof and their preparation method |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410139352.5A CN103936724B (en) | 2011-11-11 | 2011-11-11 | The fluorescent probe of test set propylhomoserin and presoma thereof and their preparation method |
| CN201110355596.3A CN102516229B (en) | 2011-11-11 | 2011-11-11 | Fluorescent probe for detecting histidine, precursor thereof and preparation methods of fluorescent probe and precursor |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110355596.3A Division CN102516229B (en) | 2011-11-11 | 2011-11-11 | Fluorescent probe for detecting histidine, precursor thereof and preparation methods of fluorescent probe and precursor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103936724A true CN103936724A (en) | 2014-07-23 |
| CN103936724B CN103936724B (en) | 2016-02-17 |
Family
ID=46287351
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110355596.3A Expired - Fee Related CN102516229B (en) | 2011-11-11 | 2011-11-11 | Fluorescent probe for detecting histidine, precursor thereof and preparation methods of fluorescent probe and precursor |
| CN201410139352.5A Expired - Fee Related CN103936724B (en) | 2011-11-11 | 2011-11-11 | The fluorescent probe of test set propylhomoserin and presoma thereof and their preparation method |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110355596.3A Expired - Fee Related CN102516229B (en) | 2011-11-11 | 2011-11-11 | Fluorescent probe for detecting histidine, precursor thereof and preparation methods of fluorescent probe and precursor |
Country Status (1)
| Country | Link |
|---|---|
| CN (2) | CN102516229B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103848787A (en) * | 2012-12-06 | 2014-06-11 | 中国科学院大连化学物理研究所 | Fluorescence probe and application thereof in reversible detection of hypochlorous acid |
| CN106867271A (en) * | 2015-12-11 | 2017-06-20 | 中国科学院大连化学物理研究所 | The naphthalimide fluorescent dyestuff and its synthetic method and application of a kind of big Stokes shift and launch wavelength long |
| CN107857750A (en) * | 2016-11-18 | 2018-03-30 | 南京工业大学 | Fluorescent probe compound and preparation and application thereof |
| CN106905418B (en) * | 2017-01-18 | 2020-10-20 | 华东理工大学 | Histidine fluorescent probe and preparation method and application thereof |
| CN114507214B (en) * | 2022-03-03 | 2023-04-28 | 河北师范大学 | Fluorescent compound, fluorescent probe, fluorescent sensing film, and preparation methods and applications thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101037595A (en) * | 2006-03-16 | 2007-09-19 | 中国科学院化学研究所 | Histindine fluorescence probe and special fluorescence compound |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101633640B (en) * | 2009-08-18 | 2011-08-03 | 华东理工大学 | Naphthalimide derivative |
-
2011
- 2011-11-11 CN CN201110355596.3A patent/CN102516229B/en not_active Expired - Fee Related
- 2011-11-11 CN CN201410139352.5A patent/CN103936724B/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101037595A (en) * | 2006-03-16 | 2007-09-19 | 中国科学院化学研究所 | Histindine fluorescence probe and special fluorescence compound |
Non-Patent Citations (1)
| Title |
|---|
| HYO SUNG JUNG, ET AL.,: "Coumarin-Derived Cu2+-Selective Fluorescence Sensor:Synthesis, Mechanisms, and Applications in Living Cells.", 《J.AM.CHEM.SOC》 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102516229B (en) | 2014-06-04 |
| CN103936724B (en) | 2016-02-17 |
| CN102516229A (en) | 2012-06-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104357044B (en) | A kind of fluorescent probe and its preparation method and application | |
| CN102516229B (en) | Fluorescent probe for detecting histidine, precursor thereof and preparation methods of fluorescent probe and precursor | |
| CN103614135B (en) | Two-photon fluorescent probe and preparation method and application thereof | |
| CN104017568B (en) | -Application of fluorescent probe containing rhodamine in detecting Hg2+ | |
| CN109336835B (en) | Fluorescent probe for detecting activity of myeloperoxidase and preparation method and application thereof | |
| CN101787218A (en) | Conjugated chain beta-N-substituted cyanine fluorescent dye | |
| CN100509817C (en) | Fluorescent probe for detecting superoxide anion free radical and synthesis method and use thereof | |
| CN102206235A (en) | Phosphorescent iridium complex capable of dissolving in water system, and preparation method thereof | |
| CN102516992A (en) | Fluorescent probe for detection Hg<2+> ion, and synthetic method and purpose thereof | |
| CN102344449B (en) | Heterocyclic-fused naphthalimide and preparation method and application thereof | |
| CN111100474B (en) | Synthetic method of cyanine dye and application of cyanine dye as acid-base response fluorescent reagent | |
| CN106800548B (en) | 8- benzimidazole quinoline Ratio-type pH probe and its preparation method and application | |
| CN104910894B (en) | Benzimidazole hERG potassium ion channel small-molecular fluorescent probe and preparation method and applications thereof | |
| CN109776379A (en) | It is a kind of to can be used for responding the near infrared fluorescent probe and preparation method thereof that in living cells and pH changes in chronic wounds development process | |
| CN106867512A (en) | A kind of Ratiometric fluorescent probe for detecting avidin and its synthetic method and application | |
| JP5261718B2 (en) | Fluorescent probe | |
| CN109265440B (en) | Preparation method of azacyclo fluorescent probe and application of azacyclo fluorescent probe in hydrogen sulfide detection | |
| CN114516850B (en) | Fluorescent probe for detecting tyrosinase and preparation method and application thereof | |
| CN103333211A (en) | Double-wavelength emitting heterobinuclear metal complex as well as preparation method and application thereof | |
| CN103435625B (en) | Red emission rhodamine ion fluorescence probe and application thereof | |
| CN106496099B (en) | The synthetic method of 2- [(2R, 6S) -6- [(2S) -2- hydroxyl -2- phenethyl] -1- methyl piperidine] -1- acetophenone | |
| CN111662316B (en) | Indole hydrogen peroxide fluorescent probe and preparation method thereof | |
| CN110642871B (en) | Large Stokes displacement deep red fluorescent probe RQNA for copper ion detection and preparation method and application thereof | |
| CN103254128A (en) | Water-soluble fluorescent probe for naked eye and light enhancement detection of mercury ions and synthesis and application thereof | |
| CN102887851B (en) | Compound 3,5-dimethyl-1H-pyrrole-2,4-diformaldehyde and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20160217 Termination date: 20191111 |