메뉴 건너뛰기




Volumn 98, Issue 2, 2013, Pages 201-211

Design of a water soluble 1,8-naphthalimide/3-hydroxy-4-pyridinone conjugate: Investigation of its spectroscopic properties at variable pH and in the presence of Fe3+, Cu2+ and Zn2+

Author keywords

3 Hydroxy 4 pyridinones; 4 Amino 1,8 naphthalimides; Fluorescence properties; Fluorescent probes; Microwave assisted synthesis; Quenching effect

Indexed keywords

3-HYDROXY-4-PYRIDINONES; 4-AMINO-1,8-NAPHTHALIMIDES; FLUORESCENCE PROPERTIES; FLUORESCENT PROBES; MICROWAVE ASSISTED SYNTHESIS; QUENCHING EFFECT;

EID: 84875334258     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2013.02.020     Document Type: Article
Times cited : (19)

References (87)
  • 1
    • 0021895138 scopus 로고
    • 2+ indicators with greatly improved fluorescence properties
    • 2+ indicators with greatly improved fluorescence properties J Biol Chem 260 1985 3440 3450
    • (1985) J Biol Chem , vol.260 , pp. 3440-3450
    • Grynkiewicz, G.1    Poenie, M.2    Tsien, R.Y.3
  • 2
    • 0019333905 scopus 로고
    • New calcium indicators and buffers with high selectivity against magnesium and protons: Design, synthesis, and properties of prototype structures
    • R.Y. Tsien New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures Biochem 19 1980 2396 2404
    • (1980) Biochem , vol.19 , pp. 2396-2404
    • Tsien, R.Y.1
  • 3
    • 77952478476 scopus 로고    scopus 로고
    • Fluorescent indicators for intracellular pH
    • J. Han, and K. Burgess Fluorescent indicators for intracellular pH Chem Rev 110 2010 2709 2728
    • (2010) Chem Rev , vol.110 , pp. 2709-2728
    • Han, J.1    Burgess, K.2
  • 5
    • 53549109430 scopus 로고    scopus 로고
    • Tools and tactics for the optical detection of mercuric ion
    • E.M. Nolan, and S.J. Lippard Tools and tactics for the optical detection of mercuric ion Chem Rev 108 2008 3443 3480
    • (2008) Chem Rev , vol.108 , pp. 3443-3480
    • Nolan, E.M.1    Lippard, S.J.2
  • 6
    • 79959420942 scopus 로고    scopus 로고
    • Strategies for in vivo imaging of enzyme activity: An overview and recent advances
    • A. Razgulin, N. Ma, and J. Rao Strategies for in vivo imaging of enzyme activity: an overview and recent advances Chem Soc Rev 40 2011 4186 4216
    • (2011) Chem Soc Rev , vol.40 , pp. 4186-4216
    • Razgulin, A.1    Ma, N.2    Rao, J.3
  • 7
    • 84862873324 scopus 로고    scopus 로고
    • Activity-based probes for the study of proteases: Recent advances and developments
    • S. Serim, U. Haedke, and S.H.L. Verhelst Activity-based probes for the study of proteases: recent advances and developments Chem Med Chem 7 2012 1146 1159
    • (2012) Chem Med Chem , vol.7 , pp. 1146-1159
    • Serim, S.1    Haedke, U.2    Verhelst, S.H.L.3
  • 8
    • 82955193156 scopus 로고    scopus 로고
    • Development of molecular imaging tools to investigate protein functions by chemical probe design
    • S. Mizukami Development of molecular imaging tools to investigate protein functions by chemical probe design Chem Pharm Bull 59 2011 1435 1446
    • (2011) Chem Pharm Bull , vol.59 , pp. 1435-1446
    • Mizukami, S.1
  • 9
    • 36549070172 scopus 로고    scopus 로고
    • Fluorescent probes for nitric oxide and hydrogen peroxide in cell signaling
    • E.W. Miller, and C.J. Chang Fluorescent probes for nitric oxide and hydrogen peroxide in cell signaling Curr Opin Chem Biol 11 2007 620 625
    • (2007) Curr Opin Chem Biol , vol.11 , pp. 620-625
    • Miller, E.W.1    Chang, C.J.2
  • 10
    • 80054879885 scopus 로고    scopus 로고
    • Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species
    • X. Chen, X. Tian, I. Shin, and J. Yoon Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species Chem Soc Rev 40 2011 4783 4804
    • (2011) Chem Soc Rev , vol.40 , pp. 4783-4804
    • Chen, X.1    Tian, X.2    Shin, I.3    Yoon, J.4
  • 11
    • 84864538442 scopus 로고    scopus 로고
    • Probing oxidative stress: Small molecule fluorescent sensors of metal ions, reactive oxygen species, and thiols
    • L.M. Hyman, and K.J. Frank Probing oxidative stress: small molecule fluorescent sensors of metal ions, reactive oxygen species, and thiols Coord Chem Rev 256 2012 2333 2356
    • (2012) Coord Chem Rev , vol.256 , pp. 2333-2356
    • Hyman, L.M.1    Frank, K.J.2
  • 12
    • 77958578610 scopus 로고    scopus 로고
    • Development of fluorescent probes for bioimaging applications
    • T. Nagano Development of fluorescent probes for bioimaging applications Proc Jpn Acad Ser B 86 2010 837 847
    • (2010) Proc Jpn Acad ser B , vol.86 , pp. 837-847
    • Nagano, T.1
  • 13
    • 79961003278 scopus 로고    scopus 로고
    • Fluorescent probes for sensing and imaging
    • T. Ueno, and T. Nagano Fluorescent probes for sensing and imaging Nat Methods 8 2011 642 645
    • (2011) Nat Methods , vol.8 , pp. 642-645
    • Ueno, T.1    Nagano, T.2
  • 14
    • 11944261083 scopus 로고
    • Molecular fluorescent signalling with 'fluor-spacer-receptor' systems: Approaches to sensing and switching devices via supramolecular photophysics
    • R.A. Bissell, A.P. de Silva, H.Q.N. Gunaratne, P.L.M. Lynch, G.E.M. Maguire, and K.R.A.S. Sandanayake Molecular fluorescent signalling with 'fluor-spacer-receptor' systems: approaches to sensing and switching devices via supramolecular photophysics Chem Soc Rev 21 1992 187 195
    • (1992) Chem Soc Rev , vol.21 , pp. 187-195
    • Bissell, R.A.1    De Silva, A.P.2    Gunaratne, H.Q.N.3    Lynch, P.L.M.4    Maguire, G.E.M.5    Sandanayake, K.R.A.S.6
  • 16
    • 11844290635 scopus 로고    scopus 로고
    • Synthesis and photophysical evaluation of charge neutral thiourea or urea based fluorescent PET sensors for bis-carboxylates and pyrophosphate
    • T. Gunnlaugsson, A.P. Davis, J.E. O'Brien, and M. Glynn Synthesis and photophysical evaluation of charge neutral thiourea or urea based fluorescent PET sensors for bis-carboxylates and pyrophosphate Org Biomol Chem 3 2005 48 56
    • (2005) Org Biomol Chem , vol.3 , pp. 48-56
    • Gunnlaugsson, T.1    Davis, A.P.2    O'Brien, J.E.3    Glynn, M.4
  • 18
    • 37049104670 scopus 로고
    • A new class of fluorescent pH indicators based on photo-induced electron transfer
    • A.P. de Silva, and R.A.D.D. Rupasinghe A new class of fluorescent pH indicators based on photo-induced electron transfer J Chem Soc Chem Commun 1985 1669 1670
    • (1985) J Chem Soc Chem Commun , pp. 1669-1670
    • De Silva, A.P.1    Rupasinghe, R.A.D.D.2
  • 19
    • 84942719154 scopus 로고
    • Fluorescent signalling crown ethers; 'Switching on' of fluorescence by alkali metal ion recognition and binding in situ
    • A.P. de Silva, and S.A. de Silva Fluorescent signalling crown ethers; 'switching on' of fluorescence by alkali metal ion recognition and binding in situ J Chem Soc Chem Commun 1986 1709 1710
    • (1986) J Chem Soc Chem Commun , pp. 1709-1710
    • De Silva, A.P.1    De Silva, S.A.2
  • 20
    • 0001409456 scopus 로고
    • Chelation-enhanced fluorescence in 9,10-bis(TMEDA)anthracene [33]
    • M.E. Huston, K.W. Haider, and A.W. Czarnik Chelation-enhanced fluorescence in 9,10-bis(TMEDA)anthracene [33] J Am Chem Soc 110 1988 4460 4462
    • (1988) J Am Chem Soc , vol.110 , pp. 4460-4462
    • Huston, M.E.1    Haider, K.W.2    Czarnik, A.W.3
  • 21
    • 0006854272 scopus 로고
    • Chemical communication in water using fluorescent chemosensors
    • A.W. Czarnik Chemical communication in water using fluorescent chemosensors Acc Chem Res 27 1994 302 308
    • (1994) Acc Chem Res , vol.27 , pp. 302-308
    • Czarnik, A.W.1
  • 22
    • 33750500366 scopus 로고    scopus 로고
    • Anion recognition and sensing in organic and aqueous media using luminescent and colorimetric sensors
    • T. Gunnlaugsson, M. Glynn, G.M. Tocci (née Hussey), P.E. Kruger, and F.M. Pfeffer Anion recognition and sensing in organic and aqueous media using luminescent and colorimetric sensors Coord Chem Rev 250 2006 3094 3117
    • (2006) Coord Chem Rev , vol.250 , pp. 3094-3117
    • Gunnlaugsson, T.1    Glynn, M.2    Tocci, G.M.3    Kruger, P.E.4    Pfeffer, F.M.5
  • 23
    • 78649304681 scopus 로고    scopus 로고
    • Colorimetric and fluorescent anion sensors: An overview of recent developments in the use of 1,8-naphthalimide-based chemosensors
    • R.M. Duke, E.B. Veale, F.M. Pfeffer, P.E. Kruger, and T. Gunnlaugsson Colorimetric and fluorescent anion sensors: an overview of recent developments in the use of 1,8-naphthalimide-based chemosensors Chem Soc Rev 39 2010 3936 3953
    • (2010) Chem Soc Rev , vol.39 , pp. 3936-3953
    • Duke, R.M.1    Veale, E.B.2    Pfeffer, F.M.3    Kruger, P.E.4    Gunnlaugsson, T.5
  • 24
    • 77956031472 scopus 로고    scopus 로고
    • "Alive" dyes as fluorescent sensors: Fluorophore, mechanism, receptor and images in living cells
    • X. Qian, Y. Xiao, Y. Xu, X. Guo, J. Qiana, and W. Zhua "Alive" dyes as fluorescent sensors: fluorophore, mechanism, receptor and images in living cells Chem Commun 46 2010 6418 6436
    • (2010) Chem Commun , vol.46 , pp. 6418-6436
    • Qian, X.1    Xiao, Y.2    Xu, Y.3    Guo, X.4    Qiana, J.5    Zhua, W.6
  • 25
    • 33847427772 scopus 로고
    • Luminescence and charge transfer. Part 3. The use of chromophores with ICT (internal charge transfer) excited states in the construction of fluorescent PET (photoinduced electron transfer) pH sensors and related absorption pH sensors with aminoalkyl side chains
    • A.P. de Silva, H.Q.N. Gunaratne, P.L.M. Lynch, A.J. Patty, and G.L. Spence Luminescence and charge transfer. Part 3. The use of chromophores with ICT (internal charge transfer) excited states in the construction of fluorescent PET (photoinduced electron transfer) pH sensors and related absorption pH sensors with aminoalkyl side chains J Chem Soc Trans 2 1993 1611 1616
    • (1993) J Chem Soc Trans 2 , pp. 1611-1616
    • De Silva, A.P.1    Gunaratne, H.Q.N.2    Lynch, P.L.M.3    Patty, A.J.4    Spence, G.L.5
  • 27
    • 15044363051 scopus 로고    scopus 로고
    • Ratiometric and selective fluorescent sensor for Cu II based on internal charge transfer (ICT)
    • Z. Xu, Y. Xiao, X. Qian, J. Cui, and D. Cui Ratiometric and selective fluorescent sensor for Cu II based on internal charge transfer (ICT) Org Lett 7 2005 889 892
    • (2005) Org Lett , vol.7 , pp. 889-892
    • Xu, Z.1    Xiao, Y.2    Qian, X.3    Cui, J.4    Cui, D.5
  • 28
    • 22244456737 scopus 로고    scopus 로고
    • Colorimetric and ratiometric fluorescent chemosensor with a large red-shift in emission: Cu(II)-only sensing by deprotonation of secondary amines as receptor conjugated to naphthalimide fluorophore
    • Z. Xu, X. Qian, and J. Cui Colorimetric and ratiometric fluorescent chemosensor with a large red-shift in emission: Cu(II)-only sensing by deprotonation of secondary amines as receptor conjugated to naphthalimide fluorophore Org Lett 7 2005 3029 3032
    • (2005) Org Lett , vol.7 , pp. 3029-3032
    • Xu, Z.1    Qian, X.2    Cui, J.3
  • 30
    • 67649373935 scopus 로고    scopus 로고
    • 2+ in aqueous solution: Unsymmetrical 4,5-diaminonaphthalimide with N-H deprotonation induced by metal ions
    • 2+ in aqueous solution: unsymmetrical 4,5-diaminonaphthalimide with N-H deprotonation induced by metal ions Org Biomol Chem 7 2009 1299 1303
    • (2009) Org Biomol Chem , vol.7 , pp. 1299-1303
    • Huang, J.1    Xu, Y.2    Qian, X.3
  • 31
    • 77953120728 scopus 로고    scopus 로고
    • Ratiometric fluorescent detection of Cu(II) in semi-aqueous solution using a two-fluorophore approach
    • N. Singh, N. Kaur, B. McCaughan, and J.F. Callan Ratiometric fluorescent detection of Cu(II) in semi-aqueous solution using a two-fluorophore approach Tetrahedron Lett 51 2010 3385 3387
    • (2010) Tetrahedron Lett , vol.51 , pp. 3385-3387
    • Singh, N.1    Kaur, N.2    McCaughan, B.3    Callan, J.F.4
  • 32
    • 84859268428 scopus 로고    scopus 로고
    • Synthesis and fluorescence sensing properties of a new naphthalimide derivative of calix[4]arene
    • O. Sahin, and M. Yilmaz Synthesis and fluorescence sensing properties of a new naphthalimide derivative of calix[4]arene Tetrahedron Lett 53 2012 2319 2324
    • (2012) Tetrahedron Lett , vol.53 , pp. 2319-2324
    • Sahin, O.1    Yilmaz, M.2
  • 33
    • 84866020854 scopus 로고    scopus 로고
    • Design and synthesis of a ratiometric fluorescent chemosensor for Cu(II) with a fluorophore hybridization approach
    • Z. Liu, C. Zhang, X. Wang, W. He, and Z. Guo Design and synthesis of a ratiometric fluorescent chemosensor for Cu(II) with a fluorophore hybridization approach Org Lett 14 2012 4378 4381
    • (2012) Org Lett , vol.14 , pp. 4378-4381
    • Liu, Z.1    Zhang, C.2    Wang, X.3    He, W.4    Guo, Z.5
  • 34
    • 0142126236 scopus 로고    scopus 로고
    • A highly selective and sensitive fluorescent PET (photoinduced electron transfer) chemosensor for Zn(II)
    • T. Gunnlaugsson, T.C. Lee, and R. Parkesh A highly selective and sensitive fluorescent PET (photoinduced electron transfer) chemosensor for Zn(II) Org Biomol Chem 1 2003 3265 3267
    • (2003) Org Biomol Chem , vol.1 , pp. 3265-3267
    • Gunnlaugsson, T.1    Lee, T.C.2    Parkesh, R.3
  • 35
    • 33846035682 scopus 로고    scopus 로고
    • Highly selective 4-amino-1,8-naphthalimide based fluorescent photoinduced electron transfer (PET) chemosensors for Zn(II) under physiological pH conditions
    • R. Parkesh, T.C. Lee, and T. Gunnlaugsson Highly selective 4-amino-1,8-naphthalimide based fluorescent photoinduced electron transfer (PET) chemosensors for Zn(II) under physiological pH conditions Org Biomol Chem 5 2007 310 317
    • (2007) Org Biomol Chem , vol.5 , pp. 310-317
    • Parkesh, R.1    Lee, T.C.2    Gunnlaugsson, T.3
  • 36
    • 1542320053 scopus 로고    scopus 로고
    • 2+ in neutral buffer aqueous solution
    • 2+ in neutral buffer aqueous solution J Am Chem Soc 126 2004 2272 2273
    • (2004) J Am Chem Soc , vol.126 , pp. 2272-2273
    • Guo, X.1    Qian, X.2    Jia, L.3
  • 37
    • 22344447711 scopus 로고    scopus 로고
    • A selective fluorescent ratiometric chemodosimeter for mercury ion
    • B. Liu, and H. Tian A selective fluorescent ratiometric chemodosimeter for mercury ion Chem Commun 2005 3156 3158
    • (2005) Chem Commun , pp. 3156-3158
    • Liu, B.1    Tian, H.2
  • 38
    • 33645453924 scopus 로고    scopus 로고
    • Two regioisomeric and exclusively selective Hg(II) sensor molecules composed of a naphthalimide fluorophore and an o-phenylenediamine derived triamide receptor
    • J. Wang, and X. Qian Two regioisomeric and exclusively selective Hg(II) sensor molecules composed of a naphthalimide fluorophore and an o-phenylenediamine derived triamide receptor Chem Commun 2006 109 111
    • (2006) Chem Commun , pp. 109-111
    • Wang, J.1    Qian, X.2
  • 39
    • 70349284885 scopus 로고    scopus 로고
    • Trace mercury(II) detection and separation in serum and water samples using a reusable bifunctional fluorescent sensor
    • C. He, W. Zhu, Y. Xu, T. Chen, and X. Qian Trace mercury(II) detection and separation in serum and water samples using a reusable bifunctional fluorescent sensor Anal Chim Acta 651 2009 227 233
    • (2009) Anal Chim Acta , vol.651 , pp. 227-233
    • He, C.1    Zhu, W.2    Xu, Y.3    Chen, T.4    Qian, X.5
  • 40
    • 80051949467 scopus 로고    scopus 로고
    • A water-soluble 1,8-naphthalimide-based 'turn on' fluorescent chemosensor for selective and sensitive recognition of mercury ion in water
    • H. Dai, and H. Xu A water-soluble 1,8-naphthalimide-based 'turn on' fluorescent chemosensor for selective and sensitive recognition of mercury ion in water Bioorg Med Chem Lett 21 2011 5141 5144
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 5141-5144
    • Dai, H.1    Xu, H.2
  • 42
  • 44
    • 84856475025 scopus 로고    scopus 로고
    • 2+ based on naphthalimide derivative by fluorescence enhancement in aqueous solution
    • 2+ based on naphthalimide derivative by fluorescence enhancement in aqueous solution Anal Chim Acta 717 2012 122 126
    • (2012) Anal Chim Acta , vol.717 , pp. 122-126
    • Li, C.Y.1    Xu, F.2    Li, Y.F.3    Zhou, K.4    Zhou, Y.5
  • 45
    • 57249086355 scopus 로고    scopus 로고
    • 2+ sensor of naphthalimide derivative based on complexation with alkynes and thio-heterocycle
    • 2+ sensor of naphthalimide derivative based on complexation with alkynes and thio-heterocycle Chem Commun 2008 6339 6341
    • (2008) Chem Commun , pp. 6339-6341
    • Duan, L.1    Xu, Y.2    Qian, X.3
  • 46
    • 75649086150 scopus 로고    scopus 로고
    • Design and synthesis of a highly sensitive off-on fluorescent chemosensor for zinc ions utilizing internal charge transfer
    • K. Hanaoka, Y. Muramatsu, Y. Urano, T. Terai, and T. Nagano Design and synthesis of a highly sensitive off-on fluorescent chemosensor for zinc ions utilizing internal charge transfer Chem Eur J 16 2010 568 572
    • (2010) Chem Eur J , vol.16 , pp. 568-572
    • Hanaoka, K.1    Muramatsu, Y.2    Urano, Y.3    Terai, T.4    Nagano, T.5
  • 47
    • 77249113873 scopus 로고    scopus 로고
    • Development of off-on fluorescent probes for heavy and transition metal ions
    • Z. Xu, S.J. Han, C. Lee, J. Yoon, and D.R. Spring Development of off-on fluorescent probes for heavy and transition metal ions Chem Commun 46 2010 1679 1681
    • (2010) Chem Commun , vol.46 , pp. 1679-1681
    • Xu, Z.1    Han, S.J.2    Lee, C.3    Yoon, J.4    Spring, D.R.5
  • 48
    • 84857040922 scopus 로고    scopus 로고
    • A colorimetric probe for copper(II) ion based on 4-amino-1,8- naphthalimide
    • H. Wang, L. Yang, W. Zhang, Y. Zhou, B. Zhao, and X. Li A colorimetric probe for copper(II) ion based on 4-amino-1,8-naphthalimide Inorg Chim Acta 381 2012 111 116
    • (2012) Inorg Chim Acta , vol.381 , pp. 111-116
    • Wang, H.1    Yang, L.2    Zhang, W.3    Zhou, Y.4    Zhao, B.5    Li, X.6
  • 49
    • 52949104778 scopus 로고    scopus 로고
    • Hydroxypyranones, hydroxypyridinones and their complexes
    • J. Burgess, and M. Rangel Hydroxypyranones, hydroxypyridinones and their complexes Adv Inorg Chem 60 2008 167 243
    • (2008) Adv Inorg Chem , vol.60 , pp. 167-243
    • Burgess, J.1    Rangel, M.2
  • 50
    • 0034683482 scopus 로고    scopus 로고
    • Mixed hydroxypyridinonate ligands as iron chelators
    • S.M. Cohen, B. O'Sullivan, and K.N. Raymond Mixed hydroxypyridinonate ligands as iron chelators Inorg Chem 39 2000 4339 4346
    • (2000) Inorg Chem , vol.39 , pp. 4339-4346
    • Cohen, S.M.1    O'Sullivan, B.2    Raymond, K.N.3
  • 51
    • 0037121863 scopus 로고    scopus 로고
    • Hexadentate hydroxypyridonate iron chelators based on TREN-Me-3,2-HOPO: Variation of cap size
    • J. Xu, B. O'Sullivan, and K.N. Raymond Hexadentate hydroxypyridonate iron chelators based on TREN-Me-3,2-HOPO: variation of cap size Inorg Chem 41 2002 6731 6742
    • (2002) Inorg Chem , vol.41 , pp. 6731-6742
    • Xu, J.1    O'Sullivan, B.2    Raymond, K.N.3
  • 52
    • 84876411168 scopus 로고    scopus 로고
    • US patent. 5 624 901
    • Raymond KN, Xu J. US patent. 5 624 901; 1997.
    • (1997)
    • Raymond, K.N.1    Xu, J.2
  • 53
    • 82355175854 scopus 로고    scopus 로고
    • Hydroxypyridinones as "privileged" chelating structures for the design of medicinal drugs
    • M.A. Santos, S.M. Marques, and S. Chaves Hydroxypyridinones as "privileged" chelating structures for the design of medicinal drugs Coord Chem Rev 256 2012 240 259
    • (2012) Coord Chem Rev , vol.256 , pp. 240-259
    • Santos, M.A.1    Marques, S.M.2    Chaves, S.3
  • 54
    • 84864566040 scopus 로고    scopus 로고
    • The art of building multifunctional metal-binding agents from basic molecular scaffolds for the potential application in neurodegenerative diseases
    • C. Rodríguez-Rodríguez, M. Telpoukhovskaia, and C. Orvig The art of building multifunctional metal-binding agents from basic molecular scaffolds for the potential application in neurodegenerative diseases Coord Chem Rev 256 2012 2308 2332
    • (2012) Coord Chem Rev , vol.256 , pp. 2308-2332
    • Rodríguez-Rodríguez, C.1    Telpoukhovskaia, M.2    Orvig, C.3
  • 55
    • 0037013658 scopus 로고    scopus 로고
    • Hydroxypyridinone complexes with aluminium. in vitro/vivo studies and perspectives
    • M.A. Santos Hydroxypyridinone complexes with aluminium. In vitro/vivo studies and perspectives Coord Chem Rev 228 2002 187 203
    • (2002) Coord Chem Rev , vol.228 , pp. 187-203
    • Santos, M.A.1
  • 56
    • 9744251550 scopus 로고    scopus 로고
    • Design, synthesis, physicochemical properties, and evaluation of novel iron chelators with fluorescent sensors
    • Y. Ma, W. Luo, P.J. Quinn, Z. Liu, and R.C. Hider Design, synthesis, physicochemical properties, and evaluation of novel iron chelators with fluorescent sensors J Med Chem 47 2004 6349 6362
    • (2004) J Med Chem , vol.47 , pp. 6349-6362
    • Ma, Y.1    Luo, W.2    Quinn, P.J.3    Liu, Z.4    Hider, R.C.5
  • 57
    • 33646872856 scopus 로고    scopus 로고
    • Synthesis of new 3-hydroxy-4(1H)-pyridinone directly attached to quinoxaline and its fluorescence property upon complexation to metal ions
    • A. Katoh, K. Ogino, and R. Saito Synthesis of new 3-hydroxy-4(1H)- pyridinone directly attached to quinoxaline and its fluorescence property upon complexation to metal ions Heterocycles 65 2005 2195 2201
    • (2005) Heterocycles , vol.65 , pp. 2195-2201
    • Katoh, A.1    Ogino, K.2    Saito, R.3
  • 58
    • 49449091809 scopus 로고    scopus 로고
    • Targeting the lysosome: Fluorescent iron(III) chelators to selectively monitor endosomal/lysosomal labile iron pools
    • S. Fakih, M. Podinovskaia, X. Kong, H.L. Collins, U.E. Schaible, and R.C. Hider Targeting the lysosome: fluorescent iron(III) chelators to selectively monitor endosomal/lysosomal labile iron pools J Med Chem 51 2008 4539 4552
    • (2008) J Med Chem , vol.51 , pp. 4539-4552
    • Fakih, S.1    Podinovskaia, M.2    Kong, X.3    Collins, H.L.4    Schaible, U.E.5    Hider, R.C.6
  • 59
    • 67049097553 scopus 로고    scopus 로고
    • Monitoring intracellular labile iron pools: A novel fluorescent iron(III) sensor as a potential non-invasive diagnosis tool
    • S. Fakih, M. Podinovskaia, X. Kong, U.E. Schaible, H.L. Collins, and R.C. Hider Monitoring intracellular labile iron pools: a novel fluorescent iron(III) sensor as a potential non-invasive diagnosis tool J Pharm Sci 98 2009 2212 2226
    • (2009) J Pharm Sci , vol.98 , pp. 2212-2226
    • Fakih, S.1    Podinovskaia, M.2    Kong, X.3    Schaible, U.E.4    Collins, H.L.5    Hider, R.C.6
  • 60
    • 84867322548 scopus 로고    scopus 로고
    • Iron(III) selective molecular and supramolecular fluorescent probes
    • S.K. Sahoo, D. Sharma, R.K. Bera, G. Crisponi, and J.F. Callan Iron(III) selective molecular and supramolecular fluorescent probes Chem Soc Rev 41 2012 7195 7227
    • (2012) Chem Soc Rev , vol.41 , pp. 7195-7227
    • Sahoo, S.K.1    Sharma, D.2    Bera, R.K.3    Crisponi, G.4    Callan, J.F.5
  • 61
    • 77649274461 scopus 로고    scopus 로고
    • Identification of a new hexadentate iron chelator capable of restricting the intramacrophagic growth of Mycobacterium avium
    • S.S. Fernandes, A. Nunes, A.R. Gomes, B. de Castro, R.C. Hider, and M. Rangel Identification of a new hexadentate iron chelator capable of restricting the intramacrophagic growth of Mycobacterium avium Microbes Infect 12 2010 287 294
    • (2010) Microbes Infect , vol.12 , pp. 287-294
    • Fernandes, S.S.1    Nunes, A.2    Gomes, A.R.3    De Castro, B.4    Hider, R.C.5    Rangel, M.6
  • 62
    • 77956481551 scopus 로고    scopus 로고
    • Fluorescent 3-hydroxy-4-pyridinone hexadentate iron chelators: Intracellular distribution and the relevance to antimycobacterial properties
    • A. Nunes, M. Podinovskaia, A. Leite, P. Gameiro, T. Zhou, and Y. Ma Fluorescent 3-hydroxy-4-pyridinone hexadentate iron chelators: intracellular distribution and the relevance to antimycobacterial properties J Biol Inorg Chem 15 2010 861 877
    • (2010) J Biol Inorg Chem , vol.15 , pp. 861-877
    • Nunes, A.1    Podinovskaia, M.2    Leite, A.3    Gameiro, P.4    Zhou, T.5    Ma, Y.6
  • 63
    • 62349102322 scopus 로고    scopus 로고
    • Novel 3-hydroxy-4-pyridinonato oxidovanadium(IV) complexes to investigate structure/activity relationships
    • M. Rangel, M.J. Amorim, A. Nunes, A. Leite, E. Pereira, and B. de Castro Novel 3-hydroxy-4-pyridinonato oxidovanadium(IV) complexes to investigate structure/activity relationships J Inorg Biochem 103 2009 496 502
    • (2009) J Inorg Biochem , vol.103 , pp. 496-502
    • Rangel, M.1    Amorim, M.J.2    Nunes, A.3    Leite, A.4    Pereira, E.5    De Castro, B.6
  • 64
    • 81055137648 scopus 로고    scopus 로고
    • Investigation of the insulin-like properties of zinc(II) complexes of 3-hydroxy-4-pyridinones: Identification of a compound with glucose lowering effect in STZ-induced type i diabetic animals
    • T. Moniz, M.J. Amorim, R. Ferreira, A. Nunes, A. Silva, and C. Queirós Investigation of the insulin-like properties of zinc(II) complexes of 3-hydroxy-4-pyridinones: identification of a compound with glucose lowering effect in STZ-induced type I diabetic animals J Biol Inorg Chem 105 2011 1675 1682
    • (2011) J Biol Inorg Chem , vol.105 , pp. 1675-1682
    • Moniz, T.1    Amorim, M.J.2    Ferreira, R.3    Nunes, A.4    Silva, A.5    Queirós, C.6
  • 65
    • 77957749950 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of 3-hydroxy-4-pyridinone/naphthalene conjugates. Structural characterization and selection of a fluorescent ion sensor
    • A.M.G. Silva, A. Leite, M. Andrade, P. Gameiro, P. Brandão, and V. Felix Microwave-assisted synthesis of 3-hydroxy-4-pyridinone/naphthalene conjugates. Structural characterization and selection of a fluorescent ion sensor Tetrahedron 66 2010 8544 8550
    • (2010) Tetrahedron , vol.66 , pp. 8544-8550
    • Silva, A.M.G.1    Leite, A.2    Andrade, M.3    Gameiro, P.4    Brandão, P.5    Felix, V.6
  • 66
    • 80052412453 scopus 로고    scopus 로고
    • Use of a porphyrin platform and 3,4-HPO chelating units to synthesize ligands with N4 and O4 coordination sites
    • A.M.G. Silva, A. Leite, P. Gonzalez, M.R.M. Domingues, P. Gameiro, and B. de Castro Use of a porphyrin platform and 3,4-HPO chelating units to synthesize ligands with N4 and O4 coordination sites Tetrahedron 67 2011 7821 7828
    • (2011) Tetrahedron , vol.67 , pp. 7821-7828
    • Silva, A.M.G.1    Leite, A.2    Gonzalez, P.3    Domingues, M.R.M.4    Gameiro, P.5    De Castro, B.6
  • 67
    • 0037203975 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of novel 2-substituted 3-hydroxypyridin-4-ones: Structure-activity investigation of metalloenzyme inhibition by iron chelators
    • Z.D. Liu, R. Kayyali, R.C. Hider, J.B. Porter, and A.E. Theobald Design, synthesis, and evaluation of novel 2-substituted 3-hydroxypyridin-4-ones: structure-activity investigation of metalloenzyme inhibition by iron chelators J Med Chem 45 2002 631 639
    • (2002) J Med Chem , vol.45 , pp. 631-639
    • Liu, Z.D.1    Kayyali, R.2    Hider, R.C.3    Porter, J.B.4    Theobald, A.E.5
  • 68
    • 69249248122 scopus 로고    scopus 로고
    • N,N-Dimethylformamide: Much more than a solvent
    • J. Muzart N,N-Dimethylformamide: much more than a solvent Tetrahedron 65 2009 8313 8323
    • (2009) Tetrahedron , vol.65 , pp. 8313-8323
    • Muzart, J.1
  • 69
    • 84865856326 scopus 로고    scopus 로고
    • N,N-dimethylformamide: A multipurpose building block
    • S. Ding, and N. Jiao N,N-dimethylformamide: a multipurpose building block Angew Chem Int Ed 51 2012 9226 9237
    • (2012) Angew Chem Int Ed , vol.51 , pp. 9226-9237
    • Ding, S.1    Jiao, N.2
  • 70
    • 36348953113 scopus 로고    scopus 로고
    • Synthesis and photophysical properties of fluorescence sensing ester- and amidoamine-functionalized 1,8-naphthalimides
    • V.B. Bojinov, N.I. Georgiev, and P.S. Nikolov Synthesis and photophysical properties of fluorescence sensing ester- and amidoamine-functionalized 1,8-naphthalimides J Photochem Photobiol A Chem 193 2008 129 138
    • (2008) J Photochem Photobiol A Chem , vol.193 , pp. 129-138
    • Bojinov, V.B.1    Georgiev, N.I.2    Nikolov, P.S.3
  • 72
    • 77957844408 scopus 로고    scopus 로고
    • N-Heteroaryl-1,8-naphthalimide fluorescent sensor for water: Molecular design, synthesis and properties
    • Z. Li, Q. Yang, R. Chang, G. Ma, M. Chen, and W. Zhang N-Heteroaryl-1,8-naphthalimide fluorescent sensor for water: molecular design, synthesis and properties Dyes Pigm 88 2011 307 314
    • (2011) Dyes Pigm , vol.88 , pp. 307-314
    • Li, Z.1    Yang, Q.2    Chang, R.3    Ma, G.4    Chen, M.5    Zhang, W.6
  • 73
    • 0008971832 scopus 로고
    • Relative fluorescence quantum yields using a computer-controlled luminescence spectrometer
    • A.T.R. Williams, S.A. Winfield, and J.N. Miller Relative fluorescence quantum yields using a computer-controlled luminescence spectrometer Analyst 108 1983 1067 1071
    • (1983) Analyst , vol.108 , pp. 1067-1071
    • Williams, A.T.R.1    Winfield, S.A.2    Miller, J.N.3
  • 75
    • 77955276024 scopus 로고    scopus 로고
    • A series of naphthalimide derivatives as intra and extracellular pH sensors
    • Y. Tian, F. Su, W. Weber, V. Nandakumar, B.R. Shumway, and Y. Jin A series of naphthalimide derivatives as intra and extracellular pH sensors Biomaterials 31 2010 7411 7422
    • (2010) Biomaterials , vol.31 , pp. 7411-7422
    • Tian, Y.1    Su, F.2    Weber, W.3    Nandakumar, V.4    Shumway, B.R.5    Jin, Y.6
  • 76
    • 1642481092 scopus 로고    scopus 로고
    • Proton "off-on" behaviour of methylpiperazinyl derivative of naphthalimide: A pH sensor based on fluorescence enhancement
    • C.G. Niu, G.M. Zeng, L.X. Chen, G.L. Shen, and R.Q. Yu Proton "off-on" behaviour of methylpiperazinyl derivative of naphthalimide: a pH sensor based on fluorescence enhancement Analyst 129 2004 20 24
    • (2004) Analyst , vol.129 , pp. 20-24
    • Niu, C.G.1    Zeng, G.M.2    Chen, L.X.3    Shen, G.L.4    Yu, R.Q.5
  • 77
    • 0030272334 scopus 로고    scopus 로고
    • Investigation of equilibria in solution. Determination of equilibrium constants with the HYPERQUAD suite of programs
    • P. Gans, A. Sabatini, and A. Vacca Investigation of equilibria in solution. Determination of equilibrium constants with the HYPERQUAD suite of programs Talanta 43 1996 1739 1753
    • (1996) Talanta , vol.43 , pp. 1739-1753
    • Gans, P.1    Sabatini, A.2    Vacca, A.3
  • 78
    • 78650664335 scopus 로고    scopus 로고
    • Nickel(II) and cobalt(II) 3-hydroxy-4-pyridinone complexes: Synthesis, characterization and speciation studies in aqueous solution
    • C. Queiros, M.J. Amorim, A. Leite, M. Ferreira, P. Gameiro, and B. Castro Nickel(II) and cobalt(II) 3-hydroxy-4-pyridinone complexes: synthesis, characterization and speciation studies in aqueous solution Eur J Inorg Chem 1 2011 131 140
    • (2011) Eur J Inorg Chem , vol.1 , pp. 131-140
    • Queiros, C.1    Amorim, M.J.2    Leite, A.3    Ferreira, M.4    Gameiro, P.5    Castro, B.6
  • 80
    • 27744586553 scopus 로고    scopus 로고
    • A ratiometric fluorescence sensor with broad dynamic range based on two pH-sensitive fluorophores
    • C.G. Niu, X.Q. Gui, G.M. Zeng, and X.Z. Yuan A ratiometric fluorescence sensor with broad dynamic range based on two pH-sensitive fluorophores Analyst 130 2005 1551 1556
    • (2005) Analyst , vol.130 , pp. 1551-1556
    • Niu, C.G.1    Gui, X.Q.2    Zeng, G.M.3    Yuan, X.Z.4
  • 81
    • 84861937012 scopus 로고    scopus 로고
    • Hydroxy(thio)pyrone and hydroxy(thio)pyridinone iron chelators: Physico-chemical properties and anti-oxidant activity
    • S. Chaves, S. Canário, M.P. Carrasco, L. Mira, and M.A. Santos Hydroxy(thio)pyrone and hydroxy(thio)pyridinone iron chelators: physico-chemical properties and anti-oxidant activity J Inorg Biochem 114 2012 38 46
    • (2012) J Inorg Biochem , vol.114 , pp. 38-46
    • Chaves, S.1    Canário, S.2    Carrasco, M.P.3    Mira, L.4    Santos, M.A.5
  • 82
    • 70349270657 scopus 로고    scopus 로고
    • Demonstration of bidirectional photoinduced electron transfer (PET) sensing in 4-amino-1,8-naphthalimide based thiourea anion sensors
    • E.B. Veale, G.M. Tocci, F.M. Pfeffer, P.E. Krugera, and T. Gunnlaugsson Demonstration of bidirectional photoinduced electron transfer (PET) sensing in 4-amino-1,8-naphthalimide based thiourea anion sensors Org Biomol Chem 7 2009 3447 3454
    • (2009) Org Biomol Chem , vol.7 , pp. 3447-3454
    • Veale, E.B.1    Tocci, G.M.2    Pfeffer, F.M.3    Krugera, P.E.4    Gunnlaugsson, T.5
  • 83
    • 58549097070 scopus 로고    scopus 로고
    • Synthesis of new amonafide analogues via coupling reaction and their cytotoxic evaluation and DNA-binding studies
    • L. Xie, Y. Xu, F. Wang, J. Liu, X. Qian, and J. Cui Synthesis of new amonafide analogues via coupling reaction and their cytotoxic evaluation and DNA-binding studies Bioorg Med Chem 17 2009 804 810
    • (2009) Bioorg Med Chem , vol.17 , pp. 804-810
    • Xie, L.1    Xu, Y.2    Wang, F.3    Liu, J.4    Qian, X.5    Cui, J.6
  • 84
    • 0036361085 scopus 로고    scopus 로고
    • Palladium-catalyzed amination of aryl bromides using temperature- controlled microwave heating
    • Y. Wan, M. Alterman, and A. Hallberg Palladium-catalyzed amination of aryl bromides using temperature-controlled microwave heating Synthesis 11 2002 1597 1600
    • (2002) Synthesis , vol.11 , pp. 1597-1600
    • Wan, Y.1    Alterman, M.2    Hallberg, A.3
  • 85
    • 0001728437 scopus 로고    scopus 로고
    • Are fluorescence quantum yields so tricky to measure? A demonstration using familiar stationery products
    • S.F. Forgues, and D. Lavabre Are fluorescence quantum yields so tricky to measure? A demonstration using familiar stationery products J Chem Educ 76 1999 1260 1264
    • (1999) J Chem Educ , vol.76 , pp. 1260-1264
    • Forgues, S.F.1    Lavabre, D.2
  • 87
    • 0033435874 scopus 로고    scopus 로고
    • Hyperquad simulation and speciation (HySS): A utility program for the investigation of equilibria involving soluble and partially soluble species
    • L. Alderighi, P. Gans, A. Ienco, D. Peters, A. Sabatini, and A. Vacca Hyperquad simulation and speciation (HySS): a utility program for the investigation of equilibria involving soluble and partially soluble species Coord Chem Rev 184 1999 311 318
    • (1999) Coord Chem Rev , vol.184 , pp. 311-318
    • Alderighi, L.1    Gans, P.2    Ienco, A.3    Peters, D.4    Sabatini, A.5    Vacca, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.