-
1
-
-
68049115101
-
-
ed. M. Goeldner and R. S. Givens, Wiley-VCH, New York
-
T. Furuta, in Dynamic Studies in Biology: Phototriggers, Photoswitches and Caged Biomolecules, ed., M. Goeldner, and, R. S. Givens, Wiley-VCH, New York, 2005
-
(2005)
Dynamic Studies in Biology: Phototriggers, Photoswitches and Caged Biomolecules
-
-
Furuta, T.1
-
2
-
-
34547638628
-
Caged compounds: Photorelease technology for control of cellular chemistry and physiology
-
G. C. R. Ellis-Davis Caged compounds: photorelease technology for control of cellular chemistry and physiology Nat. Methods 2007 4 619 628
-
(2007)
Nat. Methods
, vol.4
, pp. 619-628
-
-
Ellis-Davis, G.C.R.1
-
3
-
-
78650696318
-
Development and applications of photo-triggered theranostic agents
-
P. Rai S. Mallide X. Zheng R. Rahmanzadeh Y. Mir S. Elrington A. Khurshid T. Hasan Development and applications of photo-triggered theranostic agents Adv. Drug Deliv. Rev. 2010 62 1094 1124
-
(2010)
Adv. Drug Deliv. Rev.
, vol.62
, pp. 1094-1124
-
-
Rai, P.1
Mallide, S.2
Zheng, X.3
Rahmanzadeh, R.4
Mir, Y.5
Elrington, S.6
Khurshid, A.7
Hasan, T.8
-
4
-
-
0036007052
-
Photolabile protecting groups and linkers
-
C. G. Bochet Photolabile protecting groups and linkers J. Chem. Soc., Perkin Trans. 1 2002 125 142
-
(2002)
J. Chem. Soc., Perkin Trans. 1
, pp. 125-142
-
-
Bochet, C.G.1
-
5
-
-
79953137441
-
Photoremovable protecting groups in organic synthesis
-
V. N. R. Pillai Photoremovable protecting groups in organic synthesis Synthesis 1980 1 26
-
(1980)
Synthesis
, pp. 1-26
-
-
Pillai, V.N.R.1
-
6
-
-
33746734322
-
Biologically active molecules with a light switch
-
G. Mayer A. Heckel Biologically active molecules with a "light switch" Angew. Chem., Int. Ed. 2006 45 4900 4921
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 4900-4921
-
-
Mayer, G.1
Heckel, A.2
-
7
-
-
33748546615
-
O-Nitrobenzyl photolabile protecting groups with red-shifted absorption: Syntheses and uncaging cross-sections for one- and two-photon excitation
-
I. Aujard C. Benbrahim M. Gouget O. Ruel J.-B. Baudin P. Neveu L. Jullien o-Nitrobenzyl photolabile protecting groups with red-shifted absorption: syntheses and uncaging cross-sections for one- and two-photon excitation Chem.-Eur. J. 2006 12 6865 6879
-
(2006)
Chem.-Eur. J.
, vol.12
, pp. 6865-6879
-
-
Aujard, I.1
Benbrahim, C.2
Gouget, M.3
Ruel, O.4
Baudin, J.-B.5
Neveu, P.6
Jullien, L.7
-
8
-
-
0000624247
-
Anthraquinon-2-ylmethoxycarbonyl (Aqmoc): A new photochemically removable protecting group for alcohols
-
T. Furuta Y. Hirayama M. Iwamura Anthraquinon-2-ylmethoxycarbonyl (Aqmoc): a new photochemically removable protecting group for alcohols Org. Lett. 2001 3 1809 1812
-
(2001)
Org. Lett.
, vol.3
, pp. 1809-1812
-
-
Furuta, T.1
Hirayama, Y.2
Iwamura, M.3
-
9
-
-
84989703982
-
1-(α-Diazobenzyl)pyrene: A reagent for photolabile and fluorescent protection of carboxyl groups of amino acids and peptides
-
M. Iwamura C. Hodota M. Ishibashi 1-(α-Diazobenzyl)pyrene: a reagent for photolabile and fluorescent protection of carboxyl groups of amino acids and peptides Synlett 1991 35 36
-
(1991)
Synlett
, pp. 35-36
-
-
Iwamura, M.1
Hodota, C.2
Ishibashi, M.3
-
10
-
-
22144468808
-
Anthracene-9-methanol - A novel fluorescent phototrigger for biomolecular caging
-
A. K. Singh P. K. Khade Anthracene-9-methanol - a novel fluorescent phototrigger for biomolecular caging Tetrahedron Lett. 2005 46 5563 5566
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 5563-5566
-
-
Singh, A.K.1
Khade, P.K.2
-
11
-
-
84855459800
-
Perylen-3-ylmethyl: Fluorescent photoremovable protecting group (FPRPG) for carboxylic acids and alcohols
-
A. Jana M. Ikbal N. D. P. Singh Perylen-3-ylmethyl: fluorescent photoremovable protecting group (FPRPG) for carboxylic acids and alcohols Tetrahedron 2012 68 1128 1136
-
(2012)
Tetrahedron
, vol.68
, pp. 1128-1136
-
-
Jana, A.1
Ikbal, M.2
Singh, N.D.P.3
-
12
-
-
0032783950
-
Deactivation behavior and excited-state properties of (coumarin-4-yl)methyl derivatives. 1. Photocleavage of (7-methoxycoumarin-4-yl) methyl-caged acids with fluorescence enhancement
-
B. Schade V. Hagen R. Schmidt R. Herbrich E. Krause T. Eckardt J. Bendig Deactivation behavior and excited-state properties of (coumarin-4-yl)methyl derivatives. 1. Photocleavage of (7-methoxycoumarin-4-yl)methyl-caged acids with fluorescence enhancement J. Org. Chem. 1999 64 9109 9117
-
(1999)
J. Org. Chem.
, vol.64
, pp. 9109-9117
-
-
Schade, B.1
Hagen, V.2
Schmidt, R.3
Herbrich, R.4
Krause, E.5
Eckardt, T.6
Bendig, J.7
-
13
-
-
33845694136
-
Photocleavage studies of fluorescent amino acid conjugates bearing different types of linkages
-
A. S. C. Fonseca M. S. T. Gonçalves S. P. G. Costa Photocleavage studies of fluorescent amino acid conjugates bearing different types of linkages Tetrahedron 2007 63 1353 1359
-
(2007)
Tetrahedron
, vol.63
, pp. 1353-1359
-
-
Fonseca, A.S.C.1
Gonçalves, M.S.T.2
Costa, S.P.G.3
-
14
-
-
77956619073
-
Light-induced cleavage of model phenylalanine conjugates based on coumarins and quinolones
-
A. S. C. Fonseca M. S. T. Gonçalves S. P. G. Costa Light-induced cleavage of model phenylalanine conjugates based on coumarins and quinolones Amino Acids 2010 39 699 712
-
(2010)
Amino Acids
, vol.39
, pp. 699-712
-
-
Fonseca, A.S.C.1
Gonçalves, M.S.T.2
Costa, S.P.G.3
-
15
-
-
39149086675
-
Comparative study of polyaromatic and polyheteroaromatic fluorescent photocleavable protecting groups
-
M. J. G. Fernandes M. S. T. Gonçalves S. P. G. Costa Comparative study of polyaromatic and polyheteroaromatic fluorescent photocleavable protecting groups Tetrahedron 2008 64 3032 3038
-
(2008)
Tetrahedron
, vol.64
, pp. 3032-3038
-
-
Fernandes, M.J.G.1
Gonçalves, M.S.T.2
Costa, S.P.G.3
-
16
-
-
54549092397
-
Neurotransmitter amino acid-oxobenzo[f]benzopyran conjugates: Synthesis and photorelease studies
-
M. J. G. Fernandes M. S. T. Gonçalves S. P. G. Costa Neurotransmitter amino acid-oxobenzo[f]benzopyran conjugates: synthesis and photorelease studies Tetrahedron 2008 64 11175 11179
-
(2008)
Tetrahedron
, vol.64
, pp. 11175-11179
-
-
Fernandes, M.J.G.1
Gonçalves, M.S.T.2
Costa, S.P.G.3
-
17
-
-
77953616977
-
2-Oxo-2H-benzo[h]benzopyran as a new light sensitive protecting group for neurotransmitter amino acids
-
A. M. S. Soares S. P. G. Costa M. S. T. Gonçalves 2-Oxo-2H-benzo[h]benzopyran as a new light sensitive protecting group for neurotransmitter amino acids Amino Acids 2010 39 121 133
-
(2010)
Amino Acids
, vol.39
, pp. 121-133
-
-
Soares, A.M.S.1
Costa, S.P.G.2
Gonçalves, M.S.T.3
-
18
-
-
84862757643
-
Photorelease of amino acids from novel thioxobenzo[f]benzopyran ester conjugates
-
A. M. Piloto A. M. S. Soares S. P. G. Costa M. S. T. Gonçalves Photorelease of amino acids from novel thioxobenzo[f]benzopyran ester conjugates Amino Acids 2012 42 2275 2282
-
(2012)
Amino Acids
, vol.42
, pp. 2275-2282
-
-
Piloto, A.M.1
Soares, A.M.S.2
Costa, S.P.G.3
Gonçalves, M.S.T.4
-
19
-
-
77956617367
-
Oxazole ligth triggered protecting groups: Synthesis and photolysis of fused heteroaromatic conjugates
-
A. M. S. Soares S. P. G. Costa M. S. T. Gonçalves Oxazole ligth triggered protecting groups: synthesis and photolysis of fused heteroaromatic conjugates Tetrahedron 2010 66 8189 8195
-
(2010)
Tetrahedron
, vol.66
, pp. 8189-8195
-
-
Soares, A.M.S.1
Costa, S.P.G.2
Gonçalves, M.S.T.3
-
20
-
-
33845469221
-
Subnanosecond time-resolved fluorescence of acridine in solution
-
L. A. Diverdi M. R. Topp Subnanosecond time-resolved fluorescence of acridine in solution J. Phys. Chem. 1984 88 3447 3451
-
(1984)
J. Phys. Chem.
, vol.88
, pp. 3447-3451
-
-
Diverdi, L.A.1
Topp, M.R.2
-
22
-
-
33749518223
-
A new acridine derivative as a fluorescent chemosensor for zinc ions in a 100% aqueous solution: A comparison of binding property with anthracene derivative
-
M. S. Park K. M. K. Swamy Y. J. Lee H. N. Lee Y. J. Jang Y. H. Moon J. Yoon A new acridine derivative as a fluorescent chemosensor for zinc ions in a 100% aqueous solution: a comparison of binding property with anthracene derivative Tetrahedron Lett. 2006 47 8129 8132
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 8129-8132
-
-
Park, M.S.1
Swamy, K.M.K.2
Lee, Y.J.3
Lee, H.N.4
Jang, Y.J.5
Moon, Y.H.6
Yoon, J.7
-
23
-
-
38349061488
-
2+
-
2+ Tetrahedron Lett. 2008 49 1261 1265
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1261-1265
-
-
Lee, H.N.1
Kim, H.N.2
Swamy, K.M.K.3
Park, M.S.4
Kim, J.5
Lee, H.6
Lee, K.-H.7
Park, S.8
Yoon, J.9
-
24
-
-
79957827636
-
2+ in aqueous media
-
2+ in aqueous media Sens. Actuators, B-Chem. 2011 156 126 131
-
(2011)
Sens. Actuators, B-Chem.
, vol.156
, pp. 126-131
-
-
Wang, Y.1
Hu, X.Y.2
Wanga, L.3
Shang, Z.4
Chao, J.5
Jin, W.6
-
25
-
-
0036096683
-
Fluorimetric analysis of lipase hydrolysis of intermediate- and long-chain glycerides
-
W. Tsuzuki A. Ue A. Nagao K. Akasaka Fluorimetric analysis of lipase hydrolysis of intermediate- and long-chain glycerides Analyst 2002 127 669 673
-
(2002)
Analyst
, vol.127
, pp. 669-673
-
-
Tsuzuki, W.1
Ue, A.2
Nagao, A.3
Akasaka, K.4
-
26
-
-
79955640809
-
Highly sensitive and selective derivatization-LC method for biomolecules based on fluorescence interactions and fluorous separations
-
K. Todoroki H. Yoshida T. Hayama M. Itoyama H. Nohta M. Yamaguchi Highly sensitive and selective derivatization-LC method for biomolecules based on fluorescence interactions and fluorous separations J. Chromatogr. B 2011 879 1325 1337
-
(2011)
J. Chromatogr. B
, vol.879
, pp. 1325-1337
-
-
Todoroki, K.1
Yoshida, H.2
Hayama, T.3
Itoyama, M.4
Nohta, H.5
Yamaguchi, M.6
-
27
-
-
85004827960
-
Improved preparation of 4-(Boc-aminoacyloxymethyl)-phenylacetic acids for use in peptide-synthesis on solid supports utilizing a protecting group removable by photolysis or reduction
-
F. S. Tjoeng G. A. Heavner Improved preparation of 4-(Boc- aminoacyloxymethyl)-phenylacetic acids for use in peptide-synthesis on solid supports utilizing a protecting group removable by photolysis or reduction Synthesis 1981 897 899
-
(1981)
Synthesis
, pp. 897-899
-
-
Tjoeng, F.S.1
Heavner, G.A.2
-
28
-
-
0346569869
-
Fluorescence quantum yield determinations. 9,10-Diphenylanthracene as a reference standard in different solvents
-
J. V. Morris M. A. Mahaney J. R. Huber Fluorescence quantum yield determinations. 9,10-Diphenylanthracene as a reference standard in different solvents J. Phys. Chem. 1976 80 969 974
-
(1976)
J. Phys. Chem.
, vol.80
, pp. 969-974
-
-
Morris, J.V.1
Mahaney, M.A.2
Huber, J.R.3
-
29
-
-
0035694698
-
Protection and labeling of thymidine by a fluorescent photolabile group
-
C. Muller P. Even M.-L. Viriot M.-C. Carré Protection and labeling of thymidine by a fluorescent photolabile group Helv. Chim. Acta 2001 84 3735 3741
-
(2001)
Helv. Chim. Acta
, vol.84
, pp. 3735-3741
-
-
Muller, C.1
Even, P.2
Viriot, M.-L.3
Carré, M.-C.4
-
30
-
-
0001693302
-
Preferential solvation studies by the fluorescence lifetime of acridine in water-alcohol mixtures
-
O. Ito E. Ito Y. Yoshikawa A. Watanabe H. Kokubun Preferential solvation studies by the fluorescence lifetime of acridine in water-alcohol mixtures J. Chem. Soc., Faraday Trans. 1996 92 227 230
-
(1996)
J. Chem. Soc., Faraday Trans.
, vol.92
, pp. 227-230
-
-
Ito, O.1
Ito, E.2
Yoshikawa, Y.3
Watanabe, A.4
Kokubun, H.5
-
32
-
-
0035992534
-
Solvent effects and photophysical studies of a new class of acridine(1,8)dione dyes
-
V. Karunakaran P. Ramamurthy T. Josephrajan V. T. Ramakrishnan Solvent effects and photophysical studies of a new class of acridine(1,8)dione dyes Spectrochim. Acta, Part A 2002 58 1443 1451
-
(2002)
Spectrochim. Acta, Part A
, vol.58
, pp. 1443-1451
-
-
Karunakaran, V.1
Ramamurthy, P.2
Josephrajan, T.3
Ramakrishnan, V.T.4
-
34
-
-
77954083477
-
Base pair mismatch identification with DNA nanoswitch and long lifetime acridine fluorophore
-
C. D. McGuinness D. Keszenman-Pereyra P. Dickenson C. J. Campbell B. A. Maltman T. T. Bachmann P. Ghazal J. Crain Base pair mismatch identification with DNA nanoswitch and long lifetime acridine fluorophore Sens. Actuators, B 2010 148 342 346
-
(2010)
Sens. Actuators, B
, vol.148
, pp. 342-346
-
-
McGuinness, C.D.1
Keszenman-Pereyra, D.2
Dickenson, P.3
Campbell, C.J.4
Maltman, B.A.5
Bachmann, T.T.6
Ghazal, P.7
Crain, J.8
-
36
-
-
0037178609
-
Quenching of the excited singlet state of acridine and 10-methylacridinium cation by thio-organic compounds in aqueous solution
-
T. Pedzinski B. Marciniak G. L. Hug Quenching of the excited singlet state of acridine and 10-methylacridinium cation by thio-organic compounds in aqueous solution J. Photochem. Photobiol., A: Chem. 2002 150 21 30
-
(2002)
J. Photochem. Photobiol., A: Chem.
, vol.150
, pp. 21-30
-
-
Pedzinski, T.1
Marciniak, B.2
Hug, G.L.3
-
38
-
-
79956139703
-
Fast time-correlated single-photon counting fluorescence lifetime acquisition using a 100 MHz semiconductor excitation source
-
D. McLoskey D. Campbell A. Allison G. Hungerford Fast time-correlated single-photon counting fluorescence lifetime acquisition using a 100 MHz semiconductor excitation source Meas. Sci. Technol. 2011 22 067001
-
(2011)
Meas. Sci. Technol.
, vol.22
, pp. 067001
-
-
McLoskey, D.1
Campbell, D.2
Allison, A.3
Hungerford, G.4
|