메뉴 건너뛰기




Volumn 110, Issue , 2014, Pages 270-284

New insights into the water-solubilization of thiol-sensitive fluorogenic probes based on long-wavelength 7-hydroxycoumarin scaffolds

Author keywords

7 Hydroxycoumarins; Fluorogenic probe; Pro fluorescence; Red shift; Thiols; Water solubility

Indexed keywords

CHEMICAL MODIFICATION; FLUORESCENCE; PROBES; SCAFFOLDS; SOLUBILITY;

EID: 84905578855     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2014.02.004     Document Type: Article
Times cited : (20)

References (63)
  • 4
    • 77952824313 scopus 로고    scopus 로고
    • Fluorescent and colorimetric probes for detection of thiols
    • X. Chen, Y. Zhou, X. Peng, and J. Yoon Fluorescent and colorimetric probes for detection of thiols Chem Soc Rev 39 2010 2120 2135
    • (2010) Chem Soc Rev , vol.39 , pp. 2120-2135
    • Chen, X.1    Zhou, Y.2    Peng, X.3    Yoon, J.4
  • 5
    • 84869499365 scopus 로고    scopus 로고
    • Coumarin-derived fluorescent chemosensors
    • InTech
    • H. Li, L. Cai, and Z. Chen Coumarin-derived fluorescent chemosensors Advances in chemical sensors 2012 InTech 121 150
    • (2012) Advances in Chemical Sensors , pp. 121-150
    • Li, H.1    Cai, L.2    Chen, Z.3
  • 6
    • 84883668233 scopus 로고    scopus 로고
    • Recent progress in luminescent and colorimetric chemosensors for detection of thiols
    • H.S. Jung, X. Chen, J.S. Kim, and J. Yoon Recent progress in luminescent and colorimetric chemosensors for detection of thiols Chem Soc Rev 42 2013 6019 6031
    • (2013) Chem Soc Rev , vol.42 , pp. 6019-6031
    • Jung, H.S.1    Chen, X.2    Kim, J.S.3    Yoon, J.4
  • 7
    • 84884263310 scopus 로고    scopus 로고
    • Thiol-addition reactions and their applications in thiol recognition
    • C. Yin, F. Huo, J. Zhang, R. Martinez-Manez, Y. Yang, and H. Lv et al. Thiol-addition reactions and their applications in thiol recognition Chem Soc Rev 42 2013 6032 6059
    • (2013) Chem Soc Rev , vol.42 , pp. 6032-6059
    • Yin, C.1    Huo, F.2    Zhang, J.3    Martinez-Manez, R.4    Yang, Y.5    Lv, H.6
  • 8
    • 84862278265 scopus 로고    scopus 로고
    • A colorimetric and fluorescent chemodosimeter for discriminative and simultaneous quantification of cysteine and homocysteine
    • L. Wang, Q. Zhou, B. Zhu, L. Yan, Z. Ma, and B. Du et al. A colorimetric and fluorescent chemodosimeter for discriminative and simultaneous quantification of cysteine and homocysteine Dyes Pigm 95 2012 275 279
    • (2012) Dyes Pigm , vol.95 , pp. 275-279
    • Wang, L.1    Zhou, Q.2    Zhu, B.3    Yan, L.4    Ma, Z.5    Du, B.6
  • 9
    • 84055217360 scopus 로고    scopus 로고
    • A highly selective wavelength-ratiometric and colorimetric probe for cysteine
    • X. Zeng, X. Zhang, B. Zhu, H. Jia, and Y. Li A highly selective wavelength-ratiometric and colorimetric probe for cysteine Dyes Pigm 94 2012 10 15
    • (2012) Dyes Pigm , vol.94 , pp. 10-15
    • Zeng, X.1    Zhang, X.2    Zhu, B.3    Jia, H.4    Li, Y.5
  • 10
    • 84870696960 scopus 로고    scopus 로고
    • Highly selective and sensitive fluorescent sensing of N-acetylcysteine: Effective discrimination of N-acetylcysteine from cysteine
    • W. Dong, H. Wen, X.-F. Yang, and H. Li Highly selective and sensitive fluorescent sensing of N-acetylcysteine: effective discrimination of N-acetylcysteine from cysteine Dyes Pigm 96 2013 653 658
    • (2013) Dyes Pigm , vol.96 , pp. 653-658
    • Dong, W.1    Wen, H.2    Yang, X.-F.3    Li, H.4
  • 11
    • 84881536569 scopus 로고    scopus 로고
    • A ratiometric fluorescent probe for hydrogen sulfide based on an excited-state intramolecular proton transfer mechanism
    • Q. Huang, X.-F. Yang, and H. Li A ratiometric fluorescent probe for hydrogen sulfide based on an excited-state intramolecular proton transfer mechanism Dyes Pigm 99 2013 871 877
    • (2013) Dyes Pigm , vol.99 , pp. 871-877
    • Huang, Q.1    Yang, X.-F.2    Li, H.3
  • 12
    • 84887982947 scopus 로고    scopus 로고
    • Novel coumarin-based sensitive and selective fluorescent probes for biothiols in aqueous solution and in living cells
    • J. Li, C.-F. Zhang, Z.-Z. Ming, W.-C. Yang, and G.-F. Yang Novel coumarin-based sensitive and selective fluorescent probes for biothiols in aqueous solution and in living cells RSC Adv 3 2013 26059 26065
    • (2013) RSC Adv , vol.3 , pp. 26059-26065
    • Li, J.1    Zhang, C.-F.2    Ming, Z.-Z.3    Yang, W.-C.4    Yang, G.-F.5
  • 13
    • 84887744036 scopus 로고    scopus 로고
    • A coumarin-based fluorescent probe for biological thiols and its application for living cell imaging
    • L. Long, L. Zhou, L. Wang, S. Meng, A. Gong, and F. Du et al. A coumarin-based fluorescent probe for biological thiols and its application for living cell imaging Org Biomol Chem 11 2013 8214 8220
    • (2013) Org Biomol Chem , vol.11 , pp. 8214-8220
    • Long, L.1    Zhou, L.2    Wang, L.3    Meng, S.4    Gong, A.5    Du, F.6
  • 14
    • 84888082957 scopus 로고    scopus 로고
    • Selective fluorometric detection of aromatic thiols by a chemosensor containing two electrophilic sites with different local softness
    • Y. Shiraishi, K. Yamamoto, S. Sumiya, and T. Hirai Selective fluorometric detection of aromatic thiols by a chemosensor containing two electrophilic sites with different local softness Chem Commun 49 2013 11680 11682
    • (2013) Chem Commun , vol.49 , pp. 11680-11682
    • Shiraishi, Y.1    Yamamoto, K.2    Sumiya, S.3    Hirai, T.4
  • 15
    • 84865824408 scopus 로고    scopus 로고
    • A fluorescent sensor bearing nitroolefin moiety for the detection of thiols and its biological imaging
    • H. Wang, G. Zhou, C. Mao, and X. Chen A fluorescent sensor bearing nitroolefin moiety for the detection of thiols and its biological imaging Dyes Pigm 96 2013 232 236
    • (2013) Dyes Pigm , vol.96 , pp. 232-236
    • Wang, H.1    Zhou, G.2    Mao, C.3    Chen, X.4
  • 16
    • 84877106368 scopus 로고    scopus 로고
    • A lysosome-targetable fluorescent probe for imaging hydrogen sulfide in living cells
    • T. Liu, Z. Xu, D.R. Spring, and J. Cui A lysosome-targetable fluorescent probe for imaging hydrogen sulfide in living cells Org Lett 15 2013 2310 2313
    • (2013) Org Lett , vol.15 , pp. 2310-2313
    • Liu, T.1    Xu, Z.2    Spring, D.R.3    Cui, J.4
  • 17
    • 84882458261 scopus 로고    scopus 로고
    • A two-photon fluorescent probe for imaging hydrogen sulfide in living cells
    • T. Liu, X. Zhang, Q. Qiao, C. Zou, L. Feng, and J. Cui et al. A two-photon fluorescent probe for imaging hydrogen sulfide in living cells Dyes Pigm 99 2013 537 542
    • (2013) Dyes Pigm , vol.99 , pp. 537-542
    • Liu, T.1    Zhang, X.2    Qiao, Q.3    Zou, C.4    Feng, L.5    Cui, J.6
  • 18
    • 84890258076 scopus 로고    scopus 로고
    • A visible light excitable colorimetric and fluorescent ESIPT probe for rapid and selective detection of hydrogen sulfide
    • Y. Liu, and G. Feng A visible light excitable colorimetric and fluorescent ESIPT probe for rapid and selective detection of hydrogen sulfide Org Biomol Chem 12 2014 438 445
    • (2014) Org Biomol Chem , vol.12 , pp. 438-445
    • Liu, Y.1    Feng, G.2
  • 19
    • 84884767942 scopus 로고    scopus 로고
    • A colorimetric and fluorescent probe for thiols based on 1, 8-naphthalimide and its application for bioimaging
    • J. Shi, Y. Wang, X. Tang, W. Liu, H. Jiang, and W. Dou et al. A colorimetric and fluorescent probe for thiols based on 1, 8-naphthalimide and its application for bioimaging Dyes Pigm 100 2014 255 260
    • (2014) Dyes Pigm , vol.100 , pp. 255-260
    • Shi, J.1    Wang, Y.2    Tang, X.3    Liu, W.4    Jiang, H.5    Dou, W.6
  • 20
    • 84890810417 scopus 로고    scopus 로고
    • Bromo- and thiomaleimides as a new class of thiol-mediated fluorescence 'turn-on' reagents
    • J. Youziel, A.R. Akhbar, Q. Aziz, M.E.B. Smith, S. Caddick, and A. Tinker et al. Bromo- and thiomaleimides as a new class of thiol-mediated fluorescence 'turn-on' reagents Org Biomol Chem 12 2014 557 560
    • (2014) Org Biomol Chem , vol.12 , pp. 557-560
    • Youziel, J.1    Akhbar, A.R.2    Aziz, Q.3    Smith, M.E.B.4    Caddick, S.5    Tinker, A.6
  • 21
    • 84892778304 scopus 로고    scopus 로고
    • Simultaneous fluorescence sensing of cys and GSH from different emission channels
    • J. Liu, Y.-Q. Sun, Y. Huo, H. Zhang, L. Wang, and P. Zhang et al. Simultaneous fluorescence sensing of cys and GSH from different emission channels J Am Chem Soc 136 2014 574 577
    • (2014) J Am Chem Soc , vol.136 , pp. 574-577
    • Liu, J.1    Sun, Y.-Q.2    Huo, Y.3    Zhang, H.4    Wang, L.5    Zhang, P.6
  • 22
    • 84872002831 scopus 로고    scopus 로고
    • Far-red to near infrared analyte-responsive fluorescent probes based on organic fluorophore platforms for fluorescence imaging
    • L. Yuan, W. Lin, K. Zheng, L. He, and W. Huang Far-red to near infrared analyte-responsive fluorescent probes based on organic fluorophore platforms for fluorescence imaging Chem Soc Rev 42 2013 622 661
    • (2013) Chem Soc Rev , vol.42 , pp. 622-661
    • Yuan, L.1    Lin, W.2    Zheng, K.3    He, L.4    Huang, W.5
  • 23
    • 84889050211 scopus 로고    scopus 로고
    • Recent progress in the development of near-infrared fluorescent probes for bioimaging applications
    • Z. Guo, S. Park, J. Yoon, and I. Shin Recent progress in the development of near-infrared fluorescent probes for bioimaging applications Chem Soc Rev 43 2014 16 29
    • (2014) Chem Soc Rev , vol.43 , pp. 16-29
    • Guo, Z.1    Park, S.2    Yoon, J.3    Shin, I.4
  • 24
    • 84890681968 scopus 로고    scopus 로고
    • Design strategies for water-soluble small molecular chromogenic and fluorogenic probes
    • X. Li, X. Gao, W. Shi, and H. Ma Design strategies for water-soluble small molecular chromogenic and fluorogenic probes Chem Rev 114 2014 590 659
    • (2014) Chem Rev , vol.114 , pp. 590-659
    • Li, X.1    Gao, X.2    Shi, W.3    Ma, H.4
  • 25
    • 0000787713 scopus 로고
    • The unusually strong effect of a 4-cyano group upon electronic spectra and dissociation constants of 3 substituted 7-Hydroxy coumarins
    • O.S. Wolfbeis, E. Koller, and P. Hochmuth The unusually strong effect of a 4-cyano group upon electronic spectra and dissociation constants of 3 substituted 7-Hydroxy coumarins Bull Chem Soc Jpn 58 1985 731 734
    • (1985) Bull Chem Soc Jpn , vol.58 , pp. 731-734
    • Wolfbeis, O.S.1    Koller, E.2    Hochmuth, P.3
  • 28
    • 57249097924 scopus 로고    scopus 로고
    • Synthesis and electronic spectra of 3-hetaryl substituted coumarin derivatives 7-hydroxy-2H-chromen-2-one and 9-hydroxy-2H-benzo[f]chromen-2-one
    • T. Deligeorgiev, T. Tsvetkova, D. Ivanova, and I. Timtcheva Synthesis and electronic spectra of 3-hetaryl substituted coumarin derivatives 7-hydroxy-2H-chromen-2-one and 9-hydroxy-2H-benzo[f]chromen-2-one Color Technol 124 2008 195 203
    • (2008) Color Technol , vol.124 , pp. 195-203
    • Deligeorgiev, T.1    Tsvetkova, T.2    Ivanova, D.3    Timtcheva, I.4
  • 29
    • 43449126197 scopus 로고    scopus 로고
    • Synthesis of a new long-wavelength latent fluorimetric indicator for analytes determination in the DT-diaphorase coupling dehydrogenase assay system
    • S.T. Huang, Y.X. Peng, and K.L. Wang Synthesis of a new long-wavelength latent fluorimetric indicator for analytes determination in the DT-diaphorase coupling dehydrogenase assay system Biosens Bioelectron 23 2008 1793 1798
    • (2008) Biosens Bioelectron , vol.23 , pp. 1793-1798
    • Huang, S.T.1    Peng, Y.X.2    Wang, K.L.3
  • 30
    • 46549088880 scopus 로고    scopus 로고
    • Development of a long-wavelength fluorescent probe based on quinone-methide-type reaction to detect physiologically significant thiols
    • S.T. Huang, K.N. Ting, and K.L. Wang Development of a long-wavelength fluorescent probe based on quinone-methide-type reaction to detect physiologically significant thiols Anal Chim Acta 620 2008 120 126
    • (2008) Anal Chim Acta , vol.620 , pp. 120-126
    • Huang, S.T.1    Ting, K.N.2    Wang, K.L.3
  • 31
    • 77951199027 scopus 로고    scopus 로고
    • Photocontrolled molecular assembler based on cucurbit[8]uril: [2+2]-Autophotocycloaddition of styryl dyes in the solid state and in water
    • S.P. Gromov, A.I. Vedernikov, L.G. Kuz'mina, D.V. Kondratuk, S.K. Sazonov, and Y.A. Strelenko et al. Photocontrolled molecular assembler based on cucurbit[8]uril: [2+2]-Autophotocycloaddition of styryl dyes in the solid state and in water Eur J Org Chem 2010 2010 2587 2599
    • (2010) Eur J Org Chem , vol.2010 , pp. 2587-2599
    • Gromov, S.P.1    Vedernikov, A.I.2    Kuz'Mina, L.G.3    Kondratuk, D.V.4    Sazonov, S.K.5    Strelenko, Y.A.6
  • 33
    • 80655144856 scopus 로고    scopus 로고
    • Synthesis of novel water-soluble fluorescent coumarins bearing sulphonic and hydroxyl groups
    • T. Deligeorgiev, T. Tsvetkova, and S. Stanimirov Synthesis of novel water-soluble fluorescent coumarins bearing sulphonic and hydroxyl groups Color Technol 127 2011 434 439
    • (2011) Color Technol , vol.127 , pp. 434-439
    • Deligeorgiev, T.1    Tsvetkova, T.2    Stanimirov, S.3
  • 34
    • 79953267815 scopus 로고    scopus 로고
    • Protonation equilibria and stepwise hydrolysis behavior of a series of thiomonophosphate anions
    • H. Maki, Y. Ueda, and H. Nariai Protonation equilibria and stepwise hydrolysis behavior of a series of thiomonophosphate anions J Phys Chem B 115 2011 3571 3577
    • (2011) J Phys Chem B , vol.115 , pp. 3571-3577
    • Maki, H.1    Ueda, Y.2    Nariai, H.3
  • 35
    • 84878095829 scopus 로고    scopus 로고
    • The first comparative study of the ability of different hydrophilic groups to water-solubilise fluorescent BODIPY dyes
    • A. Romieu, C. Massif, S. Rihn, G. Ulrich, R. Ziessel, and P.-Y. Renard The first comparative study of the ability of different hydrophilic groups to water-solubilise fluorescent BODIPY dyes New J Chem 37 2013 1016 1027
    • (2013) New J Chem , vol.37 , pp. 1016-1027
    • Romieu, A.1    Massif, C.2    Rihn, S.3    Ulrich, G.4    Ziessel, R.5    Renard, P.-Y.6
  • 36
    • 84870688560 scopus 로고    scopus 로고
    • Highly selective and sensitive colourimetric detection of Hg2+ ions by unsymmetrical squaraine dyes
    • K.M. Shafeekh, M.K.A. Rahim, M.C. Basheer, C.H. Suresh, and S. Das Highly selective and sensitive colourimetric detection of Hg2+ ions by unsymmetrical squaraine dyes Dyes Pigm 96 2013 714 721
    • (2013) Dyes Pigm , vol.96 , pp. 714-721
    • Shafeekh, K.M.1    Rahim, M.K.A.2    Basheer, M.C.3    Suresh, C.H.4    Das, S.5
  • 37
    • 77951864540 scopus 로고    scopus 로고
    • NMR chemical shifts of trace impurities: Common laboratory solvents, organics, and gases in deuterated solvents relevant to the organometallic chemist
    • G.R. Fulmer, A.J.M. Miller, N.H. Sherden, H.E. Gottlieb, A. Nudelman, and B.M. Stoltz et al. NMR chemical shifts of trace impurities: common laboratory solvents, organics, and gases in deuterated solvents relevant to the organometallic chemist Organometallics 29 2010 2176 2179
    • (2010) Organometallics , vol.29 , pp. 2176-2179
    • Fulmer, G.R.1    Miller, A.J.M.2    Sherden, N.H.3    Gottlieb, H.E.4    Nudelman, A.5    Stoltz, B.M.6
  • 38
    • 0034587631 scopus 로고    scopus 로고
    • Fluorescence switching by O-dearylation of 7-aryloxycoumarins. Development of novel fluorescence probes to detect reactive oxygen species with high selectivity
    • K.-I. Setsukinai, Y. Urano, K. Kikuchi, T. Higuchi, and T. Nagano Fluorescence switching by O-dearylation of 7-aryloxycoumarins. Development of novel fluorescence probes to detect reactive oxygen species with high selectivity J Chem Soc Perkin Trans 2 2000 2453 2457 (Pubitemid 35165701)
    • (2000) Journal of the Chemical Society. Perkin Transactions 2 , Issue.12 , pp. 2453-2457
    • Setsukinai, K.-I.1    Urano, Y.2    Kikuchi, K.3    Higuchi, T.4    Nagano, T.5
  • 39
    • 84855424940 scopus 로고    scopus 로고
    • Standards for photoluminescence quantum yield measurements in solution (IUPAC technical report)
    • A.M. Brouwer Standards for photoluminescence quantum yield measurements in solution (IUPAC technical report) Pure Appl Chem 83 2011 2213 2228
    • (2011) Pure Appl Chem , vol.83 , pp. 2213-2228
    • Brouwer, A.M.1
  • 40
    • 84905563789 scopus 로고    scopus 로고
    • Determined by us in PB at 25 °C using 7-hydroxycoumarin as a standard
    • Determined by us in PB at 25°C using 7-hydroxycoumarin as a standard.
  • 41
    • 76949101068 scopus 로고    scopus 로고
    • A highly sensitive fluorescent probe for detection of benzenethiols in environmental samples and living cells
    • W. Lin, L. Long, and W. Tan A highly sensitive fluorescent probe for detection of benzenethiols in environmental samples and living cells Chem Commun 46 2010 1503 1505
    • (2010) Chem Commun , vol.46 , pp. 1503-1505
    • Lin, W.1    Long, L.2    Tan, W.3
  • 42
    • 79952818304 scopus 로고    scopus 로고
    • Development of a sensitive long-wavelength fluorogenic probe for nitroreductase: A new fluorimetric indictor for analyte determination by dehydrogenase-coupled biosensors
    • H.C. Huang, K.L. Wang, S.T. Huang, H.Y. Lin, and C.M. Lin Development of a sensitive long-wavelength fluorogenic probe for nitroreductase: a new fluorimetric indictor for analyte determination by dehydrogenase-coupled biosensors Biosens Bioelectron 26 2011 3511 3516
    • (2011) Biosens Bioelectron , vol.26 , pp. 3511-3516
    • Huang, H.C.1    Wang, K.L.2    Huang, S.T.3    Lin, H.Y.4    Lin, C.M.5
  • 43
    • 84867897819 scopus 로고    scopus 로고
    • Dual signaling of hypochlorous acid by desulfurization of thiocoumarin
    • J.O. Moon, J.W. Lee, M.G. Choi, S. Ahn, and S.-K. Chang Dual signaling of hypochlorous acid by desulfurization of thiocoumarin Tetrahedron Lett 53 2012 6594 6597
    • (2012) Tetrahedron Lett , vol.53 , pp. 6594-6597
    • Moon, J.O.1    Lee, J.W.2    Choi, M.G.3    Ahn, S.4    Chang, S.-K.5
  • 45
    • 59949093499 scopus 로고    scopus 로고
    • 3-Carboxy-6-chloro-7-hydroxycoumarin: A highly fluorescent, water-soluble violet-excitable dye for cell analysis
    • B. Abrams, Z. Diwu, O. Guryev, S. Aleshkov, R. Hingorani, and M. Edinger et al. 3-Carboxy-6-chloro-7-hydroxycoumarin: a highly fluorescent, water-soluble violet-excitable dye for cell analysis Anal Biochem 386 2009 262 269
    • (2009) Anal Biochem , vol.386 , pp. 262-269
    • Abrams, B.1    Diwu, Z.2    Guryev, O.3    Aleshkov, S.4    Hingorani, R.5    Edinger, M.6
  • 47
    • 79960342202 scopus 로고    scopus 로고
    • N-Fmoc-α-sulfo-β-alanine: A versatile building block for the water solubilization of chromophores and fluorophores by solid-phase strategy
    • A. Romieu, T. Bruckdorfer, G. Clavé, V. Grandclaude, C. Massif, and P.-Y. Renard N-Fmoc-α-sulfo-β-alanine: a versatile building block for the water solubilization of chromophores and fluorophores by solid-phase strategy Org Biomol Chem 9 2011 5337 5342
    • (2011) Org Biomol Chem , vol.9 , pp. 5337-5342
    • Romieu, A.1    Bruckdorfer, T.2    Clavé, G.3    Grandclaude, V.4    Massif, C.5    Renard, P.-Y.6
  • 48
    • 84861309047 scopus 로고    scopus 로고
    • New insights into the water-solubilisation of fluorophores by post-synthetic "click" and Sonogashira reactions
    • C. Massif, S. Dautrey, A. Haefele, R. Ziessel, P.-Y. Renard, and A. Romieu New insights into the water-solubilisation of fluorophores by post-synthetic "click" and Sonogashira reactions Org Biomol Chem 10 2012 4330 4336
    • (2012) Org Biomol Chem , vol.10 , pp. 4330-4336
    • Massif, C.1    Dautrey, S.2    Haefele, A.3    Ziessel, R.4    Renard, P.-Y.5    Romieu, A.6
  • 50
    • 77951809919 scopus 로고    scopus 로고
    • [8-[Bis(carboxymethyl)aminomethyl]-6-bromo-7-hydroxycoumarin-4-yl]methyl moieties as photoremovable protecting groups for compounds with COOH, NH2, OH, and C=O functions
    • V. Hagen, F. Kilic, J. Schaal, B. Dekowski, R. Schmidt, and N. Kotzur [8-[Bis(carboxymethyl)aminomethyl]-6-bromo-7-hydroxycoumarin-4-yl]methyl moieties as photoremovable protecting groups for compounds with COOH, NH2, OH, and C=O functions J Org Chem 75 2010 2790 2797
    • (2010) J Org Chem , vol.75 , pp. 2790-2797
    • Hagen, V.1    Kilic, F.2    Schaal, J.3    Dekowski, B.4    Schmidt, R.5    Kotzur, N.6
  • 51
    • 84878249979 scopus 로고    scopus 로고
    • New repertoire of 'donor-two-acceptor' NIR fluorogenic dyes
    • E. Kisin-Finfer, and D. Shabat New repertoire of 'donor-two-acceptor' NIR fluorogenic dyes Bioorg Med Chem 21 2013 3602 3608
    • (2013) Bioorg Med Chem , vol.21 , pp. 3602-3608
    • Kisin-Finfer, E.1    Shabat, D.2
  • 52
    • 33344466047 scopus 로고    scopus 로고
    • 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)
    • DOI 10.1055/s-2006-932456
    • S.B. Bharate 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) Synlett 2006 496 497 (Pubitemid 43288598)
    • (2006) Synlett , Issue.3 , pp. 496-497
    • Bharate, S.B.1
  • 53
    • 55449090590 scopus 로고    scopus 로고
    • 7-Hydroxycoumarin-hemicyanine hybrids: A new class of far-red emitting fluorogenic dyes
    • J.-A. Richard, M. Massonneau, P.-Y. Renard, and A. Romieu 7-Hydroxycoumarin-hemicyanine hybrids: a new class of far-red emitting fluorogenic dyes Org Lett 10 2008 4175 4178
    • (2008) Org Lett , vol.10 , pp. 4175-4178
    • Richard, J.-A.1    Massonneau, M.2    Renard, P.-Y.3    Romieu, A.4
  • 54
    • 84862525735 scopus 로고    scopus 로고
    • A new ratiometric and colorimetric chemosensor for cyanide anion based on coumarin-hemicyanine hybrid
    • Z. Yang, Z. Liu, Y. Chen, X. Wang, W. He, and Y. Lu A new ratiometric and colorimetric chemosensor for cyanide anion based on coumarin-hemicyanine hybrid Org Biomol Chem 10 2012 5073 5076
    • (2012) Org Biomol Chem , vol.10 , pp. 5073-5076
    • Yang, Z.1    Liu, Z.2    Chen, Y.3    Wang, X.4    He, W.5    Lu, Y.6
  • 55
    • 84905593106 scopus 로고    scopus 로고
    • © 1994-2013 ACD/Labs)
    • © 1994-2013 ACD/Labs).
  • 56
    • 84996394469 scopus 로고
    • Application of complementary tristimulus colorimetry to the simultaneous determination of phenol derivatives
    • H. Okuda, T. Fujimoto, M. Kawamura, and S. Hirose Application of complementary tristimulus colorimetry to the simultaneous determination of phenol derivatives Bunseki Kagaku 23 1974 644 649
    • (1974) Bunseki Kagaku , vol.23 , pp. 644-649
    • Okuda, H.1    Fujimoto, T.2    Kawamura, M.3    Hirose, S.4
  • 57
    • 79960575975 scopus 로고    scopus 로고
    • Suitable labels for molecular imaging - Influence of dye structure and hydrophilicity on the spectroscopic properties of IgG conjugates
    • J. Pauli, M. Grabolle, R. Brehm, M. Spieles, F.M. Hamann, and M. Wenzel et al. Suitable labels for molecular imaging - influence of dye structure and hydrophilicity on the spectroscopic properties of IgG conjugates Bioconjug Chem 22 2011 1298 1308
    • (2011) Bioconjug Chem , vol.22 , pp. 1298-1308
    • Pauli, J.1    Grabolle, M.2    Brehm, R.3    Spieles, M.4    Hamann, F.M.5    Wenzel, M.6
  • 58
    • 84892874974 scopus 로고    scopus 로고
    • A near-infrared colorimetric fluorescent chemodosimeter for the detection of glutathione in living cells
    • M. Li, X. Wu, Y. Wang, Y. Li, W. Zhu, and T.D. James A near-infrared colorimetric fluorescent chemodosimeter for the detection of glutathione in living cells Chem Commun 50 2014 1751 1753
    • (2014) Chem Commun , vol.50 , pp. 1751-1753
    • Li, M.1    Wu, X.2    Wang, Y.3    Li, Y.4    Zhu, W.5    James, T.D.6
  • 59
    • 84867861815 scopus 로고    scopus 로고
    • Trimethyl lock: A trigger for molecular release in chemistry, biology, and pharmacology
    • M.N. Levine, and R.T. Raines Trimethyl lock: a trigger for molecular release in chemistry, biology, and pharmacology Chem Sci 3 2012 2412 2420
    • (2012) Chem Sci , vol.3 , pp. 2412-2420
    • Levine, M.N.1    Raines, R.T.2
  • 60
    • 77950321217 scopus 로고    scopus 로고
    • A comparative study of the self-immolation of para-aminobenzylalcohol and hemithioaminal-based linkers in the context of protease-sensitive fluorogenic probes
    • Y. Meyer, J.-A. Richard, B. Delest, P. Noack, P.-Y. Renard, and A. Romieu A comparative study of the self-immolation of para-aminobenzylalcohol and hemithioaminal-based linkers in the context of protease-sensitive fluorogenic probes Org Biomol Chem 8 2010 1777 1780
    • (2010) Org Biomol Chem , vol.8 , pp. 1777-1780
    • Meyer, Y.1    Richard, J.-A.2    Delest, B.3    Noack, P.4    Renard, P.-Y.5    Romieu, A.6
  • 61
    • 79959790583 scopus 로고    scopus 로고
    • "turn-on" fluorescent sensing with "reactive" probes
    • M. Eun Jun, B. Roy, and K. Han Ahn "Turn-on" fluorescent sensing with "reactive" probes Chem Commun 47 2011 7583 7601
    • (2011) Chem Commun , vol.47 , pp. 7583-7601
    • Eun Jun, M.1    Roy, B.2    Han Ahn, K.3
  • 62
    • 84870168520 scopus 로고    scopus 로고
    • Reaction-based small-molecule fluorescent probes for chemoselective bioimaging
    • J. Chan, S.C. Dodani, and C.J. Chang Reaction-based small-molecule fluorescent probes for chemoselective bioimaging Nat Chem 4 2012 973 984
    • (2012) Nat Chem , vol.4 , pp. 973-984
    • Chan, J.1    Dodani, S.C.2    Chang, C.J.3
  • 63
    • 84864655036 scopus 로고    scopus 로고
    • Spectroscopic probes with changeable π-conjugated systems
    • W. Shi, and H. Ma Spectroscopic probes with changeable π-conjugated systems Chem Commun 48 2012 8732 8744
    • (2012) Chem Commun , vol.48 , pp. 8732-8744
    • Shi, W.1    Ma, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.