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Volumn 86, Issue 6, 2010, Pages 1247-1254

The α,5-dicarboxy-2-nitrobenzyl caging group, a tool for biophysical applications with improved hydrophilicity: Synthesis, photochemical properties and biological characterization

Author keywords

[No Author keywords available]

Indexed keywords

NITROBENZENE DERIVATIVE;

EID: 78649647595     PISSN: 00318655     EISSN: 17511097     Source Type: Journal    
DOI: 10.1111/j.1751-1097.2010.00803.x     Document Type: Article
Times cited : (6)

References (70)
  • 1
    • 84981754683 scopus 로고
    • Chemische Lichtwirkungen
    • Silber, P., and, G. Ciamician, (1901) Chemische Lichtwirkungen. Chem. Ber. 34, 2040-2046.
    • (1901) Chem. Ber. , vol.34 , pp. 2040-2046
    • Silber, P.1    Ciamician, G.2
  • 4
    • 34347345767 scopus 로고
    • Photosensitive protecting groups
    • Barltrop, J. A., and, P. Schofield, (1962) Photosensitive protecting groups. Tetrahedron Lett. 3, 697-699.
    • (1962) Tetrahedron Lett , vol.3 , pp. 697-699
    • Barltrop, J.A.1    Schofield, P.2
  • 5
    • 0017834508 scopus 로고
    • Synthesis and application of photolabile guanosine 3′,5′- phosphoric-o-nitrobenzylester
    • Engels, J., and, R. Reidys, (1978) Synthesis and application of photolabile guanosine 3′,5′-phosphoric-o-nitrobenzylester. Experientia 34, 14-15.
    • (1978) Experientia , vol.34 , pp. 14-15
    • Engels, J.1    Reidys, R.2
  • 6
    • 0017684571 scopus 로고
    • Synthesis, structure, and reactivity of adenosine cyclic 3′,5′-phosphate benzyl triesters
    • Engels, J., and, E. J. Schlaeger, (1977) Synthesis, structure, and reactivity of adenosine cyclic 3′,5′-phosphate benzyl triesters. J. Med. Chem. 20, 907-911.
    • (1977) J. Med. Chem. , vol.20 , pp. 907-911
    • Engels, J.1    Schlaeger, E.J.2
  • 7
    • 0017867017 scopus 로고
    • Rapid photolytic release of adenosine 5′-triphosphate from a protected analog-Utilization by Na-K pump of human red blood-cell ghosts
    • Kaplan, J. H., B. Forbush, and, J. F. Hoffman, (1978) Rapid photolytic release of adenosine 5′-triphosphate from a protected analog-Utilization by Na-K pump of human red blood-cell ghosts. Biochemistry 17, 1929-1935.
    • (1978) Biochemistry , vol.17 , pp. 1929-1935
    • Kaplan, J.H.1    Forbush, B.2    Hoffman, J.F.3
  • 8
    • 0018627974 scopus 로고
    • Acetylcholine receptor-controlled ion fluxes in membrane-vesicles investigated by fast reaction techniques
    • Hess, G. P., D. J. Cash, and, H. Aoshima, (1979) Acetylcholine receptor-controlled ion fluxes in membrane-vesicles investigated by fast reaction techniques. Nature 282, 329-331.
    • (1979) Nature , vol.282 , pp. 329-331
    • Hess, G.P.1    Cash, D.J.2    Aoshima, H.3
  • 9
    • 0023516913 scopus 로고
    • Chemical kinetic measurements of a mammalian acetylcholine-receptor by a fast-reaction technique
    • Udgaonkar, J. B., and, G. P. Hess, (1987) Chemical kinetic measurements of a mammalian acetylcholine-receptor by a fast-reaction technique. Proc. Natl Acad. Sci. USA 84, 8758-8762.
    • (1987) Proc. Natl Acad. Sci. USA , vol.84 , pp. 8758-8762
    • Udgaonkar, J.B.1    Hess, G.P.2
  • 10
    • 0027200349 scopus 로고
    • Caged phenylephidrine-Development and application to probe the mechanism of α-receptor mediated vasoconstriction
    • Muralidharan, S., G. M. Maher, W. A. Boyle, and, J. M. Nerbonne, (1993) Caged phenylephidrine-Development and application to probe the mechanism of α-receptor mediated vasoconstriction. Proc. Natl Acad. Sci. USA 90, 5199-5203.
    • (1993) Proc. Natl Acad. Sci. USA , vol.90 , pp. 5199-5203
    • Muralidharan, S.1    Maher, G.M.2    Boyle, W.A.3    Nerbonne, J.M.4
  • 11
    • 0027523183 scopus 로고
    • Rapid release of an α-adrenergic receptor ligand from photolabile analogs
    • Walker, J. W., H. Martin, F. R. Schmitt, and, R. J. Barsotti, (1993) Rapid release of an α-adrenergic receptor ligand from photolabile analogs. Biochemistry 32, 1338-1345.
    • (1993) Biochemistry , vol.32 , pp. 1338-1345
    • Walker, J.W.1    Martin, H.2    Schmitt, F.R.3    Barsotti, R.J.4
  • 12
    • 0028566545 scopus 로고
    • Photolabile precursors of glutamate-Synthesis, photochemical properties, and activation of glutamate receptors on a microsecond time-scale
    • Wieboldt, R., K. R. Gee, L. Niu, D. Ramesh, B. K. Carpenter, and, G. P. Hess, (1994) Photolabile precursors of glutamate-Synthesis, photochemical properties, and activation of glutamate receptors on a microsecond time-scale. Proc. Natl Acad. Sci. USA 91, 8752-8756.
    • (1994) Proc. Natl Acad. Sci. USA , vol.91 , pp. 8752-8756
    • Wieboldt, R.1    Gee, K.R.2    Niu, L.3    Ramesh, D.4    Carpenter, B.K.5    Hess, G.P.6
  • 13
    • 0028212627 scopus 로고
    • Synthesis and photochemistry of photolabile derivatives of gamma-aminobutyric-acid for chemical kinetic investigations of the gamma-aminobutyric-acid receptor in the millisecond time region
    • Wieboldt, R., D. Ramesh, B. K. Carpenter, and, G. P. Hess, (1994) Synthesis and photochemistry of photolabile derivatives of gamma-aminobutyric- acid for chemical kinetic investigations of the gamma-aminobutyric-acid receptor in the millisecond time region. Biochemistry 33, 1526-1533.
    • (1994) Biochemistry , vol.33 , pp. 1526-1533
    • Wieboldt, R.1    Ramesh, D.2    Carpenter, B.K.3    Hess, G.P.4
  • 14
    • 0040953275 scopus 로고    scopus 로고
    • A new photolabile precursor of glycine with improved properties: A tool for chemical kinetic investigations of the glycine receptor
    • Grewer, C., J. Jäger, B. K. Carpenter, and, G. P. Hess, (2000) A new photolabile precursor of glycine with improved properties: A tool for chemical kinetic investigations of the glycine receptor. Biochemistry 39, 2063-2070.
    • (2000) Biochemistry , vol.39 , pp. 2063-2070
    • Grewer, C.1    Jäger, J.2    Carpenter, B.K.3    Hess, G.P.4
  • 16
    • 36849143872 scopus 로고
    • Actin tracks-Reply
    • Theriot, J., and, T. Mitchison, (1991) Actin tracks-Reply. Nature 354, 363-363.
    • (1991) Nature , vol.354 , pp. 363-363
    • Theriot, J.1    Mitchison, T.2
  • 17
    • 0031799827 scopus 로고    scopus 로고
    • Use of caged nucleotides to characterize unstable intermediates by X-ray crystallography
    • In (Edited by G. Mariott). Academic Press, Orlando, Florida. Methods Enzymol
    • Scheidig, A. J., C. Burmester, and, R. S. Goody, (1998) Use of caged nucleotides to characterize unstable intermediates by X-ray crystallography. In Caged Compounds (Edited by, G. Mariott,). Academic Press, Orlando, Florida. Methods Enzymol. 291, 251-264.
    • (1998) Caged Compounds , vol.291 , pp. 251-264
    • Scheidig, A.J.1    Burmester, C.2    Goody, R.S.3
  • 18
    • 0036007052 scopus 로고    scopus 로고
    • Photolabile protecting groups and linkers
    • Bochet, C. G., (2002) Photolabile protecting groups and linkers. J. Chem. Soc., Perkin Trans. 1, 125-142.
    • (2002) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 125-142
    • Bochet, C.G.1
  • 19
    • 84889851263 scopus 로고    scopus 로고
    • Photoremovable protecting groups in DNA synthesis and microarray fabrication
    • In (Edited by M. Göldner and R. S. Givens), pp. Wiley, New York
    • Pirrung, M. C., and, V. S. Rana, (2005) Photoremovable protecting groups in DNA synthesis and microarray fabrication. In Dynamic Studies in Biology: Phototriggers, Photoswitches and Caged Compounds (Edited by, M. Göldner, and, R. S. Givens,), pp. 341-368. Wiley, New York.
    • (2005) Dynamic Studies in Biology: Phototriggers, Photoswitches and Caged Compounds , pp. 341-368
    • Pirrung, M.C.1    Rana, V.S.2
  • 21
    • 0041815646 scopus 로고    scopus 로고
    • Academic Press, San Diego, London, Boston, New York, Sydney, Tokyo, Toronto
    • Marriott, G., (1998) Caged Compounds. Academic Press, San Diego, London, Boston, New York, Sydney, Tokyo, Toronto.
    • (1998) Caged Compounds
    • Marriott, G.1
  • 22
    • 33746734322 scopus 로고    scopus 로고
    • Biologically active molecules with a "light switch."
    • Mayer, G., and, A. Heckel, (2006) Biologically active molecules with a "light switch." Angew. Chem. Int. Ed. 45, 4900-4921.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 4900-4921
    • Mayer, G.1    Heckel, A.2
  • 23
    • 0029894753 scopus 로고    scopus 로고
    • Caged compounds of hydrolysis-resistant analogues of cAMP and cGMP: Synthesis and application to cyclic nucleotide-gated channels
    • Hagen, V., C. Dzeja, S. Frings, J. Bendig, E. Krause, and, U. B. Kaupp, (1996) Caged compounds of hydrolysis-resistant analogues of cAMP and cGMP: Synthesis and application to cyclic nucleotide-gated channels. Biochemistry 35, 7762-7771.
    • (1996) Biochemistry , vol.35 , pp. 7762-7771
    • Hagen, V.1    Dzeja, C.2    Frings, S.3    Bendig, J.4    Krause, E.5    Kaupp, U.B.6
  • 25
    • 0030032152 scopus 로고    scopus 로고
    • Synthesis and photochemical properties of a kainate precursor and activation of kainate and AMPA receptor channels on a microsecond time scale
    • Niu, L., K. R. Gee, K. Schaper, and, G. P. Hess, (1996) Synthesis and photochemical properties of a kainate precursor and activation of kainate and AMPA receptor channels on a microsecond time scale. Biochemistry 35, 2030-2036.
    • (1996) Biochemistry , vol.35 , pp. 2030-2036
    • Niu, L.1    Gee, K.R.2    Schaper, K.3    Hess, G.P.4
  • 26
    • 0028857286 scopus 로고
    • Phosphomonoesters and phosphodiesters derived from the photohydrolysis of 2-methoxy-5-nitrophenyl substituted phosphotriesters
    • Graciani, N. R., D. S. Swanson, and, J. W. Kelly, (1995) Phosphomonoesters and phosphodiesters derived from the photohydrolysis of 2-methoxy-5-nitrophenyl substituted phosphotriesters. Tetrahedron 51, 1077-1086.
    • (1995) Tetrahedron , vol.51 , pp. 1077-1086
    • Graciani, N.R.1    Swanson, D.S.2    Kelly, J.W.3
  • 28
    • 0032854627 scopus 로고    scopus 로고
    • The use of caged adenine nucleotides and caged phosphate in intact skeletal muscle fibres of the mouse
    • Allen, D. G., J. Lannergren, and, H. Westerblad, (1999) The use of caged adenine nucleotides and caged phosphate in intact skeletal muscle fibres of the mouse. Acta Physiol. Scand. 166, 341-347.
    • (1999) Acta Physiol. Scand. , vol.166 , pp. 341-347
    • Allen, D.G.1    Lannergren, J.2    Westerblad, H.3
  • 29
    • 0029865909 scopus 로고    scopus 로고
    • Desyl esters of amino acid neurotransmitters. Phototriggers for biologically active neurotransmitters
    • Gee, K. R., L. W. Kueper, J. Barnes, G. Dudley, and, R. S. Givens, (1996) Desyl esters of amino acid neurotransmitters. Phototriggers for biologically active neurotransmitters. J. Org. Chem. 61, 1228-1233.
    • (1996) J. Org. Chem. , vol.61 , pp. 1228-1233
    • Gee, K.R.1    Kueper, L.W.2    Barnes, J.3    Dudley, G.4    Givens, R.S.5
  • 31
    • 0000897083 scopus 로고
    • Photochemistry of phosphate-esters-α-Keto phosphates as a photoprotecting group for caged phosphate
    • Givens, R. S., P. S. Athey, B. Matuszewski, L. W. Kueper, J. Y. Xue, and, T. Fister, (1993) Photochemistry of phosphate-esters-α-Keto phosphates as a photoprotecting group for caged phosphate. J. Am. Chem. Soc. 115, 6001-6012.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 6001-6012
    • Givens, R.S.1    Athey, P.S.2    Matuszewski, B.3    Kueper, L.W.4    Xue, J.Y.5    Fister, T.6
  • 32
    • 0031798357 scopus 로고    scopus 로고
    • New photoprotecting groups: Desyl- and p-hydroxyphenacyl phosphate and carboxylate esters
    • In (Edited by G. Marriott). Academic Press, San Diego, London, Boston, New York, Sydney, Tokyo, Toronto, Methods Enzymol
    • Givens, R. S., J. F. W. Weber, A. H. Jung, and, C.-H. Park,. (1998) New photoprotecting groups: desyl- and p-hydroxyphenacyl phosphate and carboxylate esters. In Caged Compounds (Edited by, G. Marriott,). Academic Press, San Diego, London, Boston, New York, Sydney, Tokyo, Toronto, Methods Enzymol. 291, 1-29.
    • (1998) Caged Compounds , vol.291 , pp. 1-29
    • Givens, R.S.1    Weber, J.F.W.2    Jung, A.H.3    Park, C.-H.4
  • 33
    • 0030907953 scopus 로고    scopus 로고
    • New photoactivated protecting groups.6. p-hydroxyphenacyl: A phototrigger for chemical and biochemical probes
    • Park, C. H., and, R. S. Givens, (1997) New photoactivated protecting groups.6. p-hydroxyphenacyl: A phototrigger for chemical and biochemical probes. J. Am. Chem. Soc. 119, 2453-2463.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2453-2463
    • Park, C.H.1    Givens, R.S.2
  • 34
    • 0034895535 scopus 로고    scopus 로고
    • Photolabile protecting groups for nucleosides: Mechanistic studies of the 2-(2-nitrophenyl)ethyl group
    • Walbert, S., W. Pfleiderer, and, U. E. Steiner, (2001) Photolabile protecting groups for nucleosides: Mechanistic studies of the 2-(2-nitrophenyl)ethyl group. Helv. Chim. Acta 84, 1601-1611.
    • (2001) Helv. Chim. Acta , vol.84 , pp. 1601-1611
    • Walbert, S.1    Pfleiderer, W.2    Steiner, U.E.3
  • 37
    • 14644392152 scopus 로고    scopus 로고
    • Synthesis and characterization of 4-methoxy-7-nitroindolinyl-D-aspartate, a caged compound for selective activation of glutamate transporters and N-methyl-D-aspartate receptors in brain tissue
    • Huang, Y. H. H., S. R. Sinha, O. D. Fedoryak, G. C. R. Ellis-Davies, and, D. E. Bergles, (2005) Synthesis and characterization of 4-methoxy-7- nitroindolinyl-D-aspartate, a caged compound for selective activation of glutamate transporters and N-methyl-D-aspartate receptors in brain tissue. Biochemistry 44, 3316-3326.
    • (2005) Biochemistry , vol.44 , pp. 3316-3326
    • Huang, Y.H.H.1    Sinha, S.R.2    Fedoryak, O.D.3    Ellis-Davies, G.C.R.4    Bergles, D.E.5
  • 38
    • 0035889780 scopus 로고    scopus 로고
    • Photochemical and pharmacological evaluation of 7-nitroindolinyl-and 4-methoxy-7-nitroindolinyl-amino acids as novel, fast caged neurotransmitters
    • Canepari, M., L. Nelson, G. Papageorgiou, J. E. T. Corrie, and, D. Ogden, (2001) Photochemical and pharmacological evaluation of 7-nitroindolinyl-and 4-methoxy-7-nitroindolinyl-amino acids as novel, fast caged neurotransmitters. J. Neurosci. Methods 112, 29-42.
    • (2001) J. Neurosci. Methods , vol.112 , pp. 29-42
    • Canepari, M.1    Nelson, L.2    Papageorgiou, G.3    Corrie, J.E.T.4    Ogden, D.5
  • 39
    • 4243836107 scopus 로고    scopus 로고
    • Pharmacological evaluation of 7-nitroindoline-caged neurotransmitters and 4-methoxy-7-nitroindoline-caged L-glutamate
    • Canepari, M., L. Nelson, G. Papageorgiou, J. E. T. Corrie, and, D. Ogden, (2001) Pharmacological evaluation of 7-nitroindoline-caged neurotransmitters and 4-methoxy-7-nitroindoline-caged L-glutamate. Biophys. J. 80, 484.
    • (2001) Biophys. J. , vol.80 , pp. 484
    • Canepari, M.1    Nelson, L.2    Papageorgiou, G.3    Corrie, J.E.T.4    Ogden, D.5
  • 40
    • 53849105450 scopus 로고    scopus 로고
    • {7-[bis(carboxymethyl)amino]coumarin-4-yl}methoxycarbonyl derivatives for photorelease of carboxylic acids, alcohols/phenols, thioalcohols/thiophenols, and amines
    • Hagen, V., B. Dekowski, N. Kotzur, R. Lechler, B. Wiesner, B. Briand, and, M. Beyermann, (2008) {7-[bis(carboxymethyl)amino]coumarin-4-yl} methoxycarbonyl derivatives for photorelease of carboxylic acids, alcohols/phenols, thioalcohols/thiophenols, and amines. Chem. Eur. J. 14, 1621-1627.
    • (2008) Chem. Eur. J. , vol.14 , pp. 1621-1627
    • Hagen, V.1    Dekowski, B.2    Kotzur, N.3    Lechler, R.4    Wiesner, B.5    Briand, B.6    Beyermann, M.7
  • 41
    • 34547398009 scopus 로고    scopus 로고
    • Mechanism of photocleavage of (coumarin-4-yl)methyl esters
    • Schmidt, R., D. Geissler, V. Hagen, and, J. Bendig, (2007) Mechanism of photocleavage of (coumarin-4-yl)methyl esters. J. Phys. Chem. A 111, 5768-5774.
    • (2007) J. Phys. Chem. A , vol.111 , pp. 5768-5774
    • Schmidt, R.1    Geissler, D.2    Hagen, V.3    Bendig, J.4
  • 43
    • 21644485711 scopus 로고    scopus 로고
    • Kinetics study of the photocleavage of (coumarin-4-yl)methyl esters
    • Schmidt, R., D. Geissler, V. Hagen, and, J. Bendig, (2005) Kinetics study of the photocleavage of (coumarin-4-yl)methyl esters. J. Phys. Chem. A 109, 5000-5004.
    • (2005) J. Phys. Chem. A , vol.109 , pp. 5000-5004
    • Schmidt, R.1    Geissler, D.2    Hagen, V.3    Bendig, J.4
  • 44
    • 15444376911 scopus 로고    scopus 로고
    • (Coumarin-4-yl)methyl esters as highly efficient, ultrafast phototriggers for protons and their application to acidifying membrane surfaces
    • Geissler, D., Y. N. Antonenko, R. Schmidt, S. Keller, O. O. Krylova, B. Wiesner, J. Bendig, P. Pohl, and, V. Hagen, (2005) (Coumarin-4-yl)methyl esters as highly efficient, ultrafast phototriggers for protons and their application to acidifying membrane surfaces. Angew. Chem. Int. Ed. 44, 1195-1198.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1195-1198
    • Geissler, D.1    Antonenko, Y.N.2    Schmidt, R.3    Keller, S.4    Krylova, O.O.5    Wiesner, B.6    Bendig, J.7    Pohl, P.8    Hagen, V.9
  • 45
    • 0037573627 scopus 로고    scopus 로고
    • 7-(dialkylamino)coumarin-4-yl]methyl-caged compounds as ultrafast and effective long-wavelength phototriggers of 8-bromo-substituted cyclic nucleotides
    • Hagen, V., S. Frings, B. Wiesner, S. Helm, U. B. Kaupp, and, J. Bendig, (2003) [7-(dialkylamino)coumarin-4-yl]methyl-caged compounds as ultrafast and effective long-wavelength phototriggers of 8-bromo-substituted cyclic nucleotides. Chembiochem 4, 434-442.
    • (2003) Chembiochem , vol.4 , pp. 434-442
    • Hagen, V.1    Frings, S.2    Wiesner, B.3    Helm, S.4    Kaupp, U.B.5    Bendig, J.6
  • 46
    • 18744416834 scopus 로고    scopus 로고
    • Synthesis of caged nucleosides with photoremovable protecting groups linked to intramolecular antennae
    • Smirnova, J., D. Wöll, W. Pfleiderer, and, U. E. Steiner, (2005) Synthesis of caged nucleosides with photoremovable protecting groups linked to intramolecular antennae. Helv. Chim. Acta 88, 891-904.
    • (2005) Helv. Chim. Acta , vol.88 , pp. 891-904
    • Smirnova, J.1    Wöll, D.2    Pfleiderer, W.3    Steiner, U.E.4
  • 47
    • 35048851485 scopus 로고    scopus 로고
    • On the mechanism of intramolecular sensitization of photocleavage of the 2-(2-nitrophenyl)propoxycarbonyl (NPPOC) protecting group
    • Wöll, D., S. Laimgruber, M. Galetskaya, J. Smirnova, W. Pfleiderer, B. Heinz, P. Gilch, and, U. E. Steiner, (2007) On the mechanism of intramolecular sensitization of photocleavage of the 2-(2-nitrophenyl) propoxycarbonyl (NPPOC) protecting group. J. Am. Chem. Soc. 129, 12148-12158.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12148-12158
    • Wöll, D.1    Laimgruber, S.2    Galetskaya, M.3    Smirnova, J.4    Pfleiderer, W.5    Heinz, B.6    Gilch, P.7    Steiner, U.E.8
  • 49
    • 27144493311 scopus 로고    scopus 로고
    • Effects of 4,5-dimethoxy groups on the time-resolved photoconversion of 2-nitrobenzyl alcohols and 2-nitrobenzaldehyde into nitroso derivatives
    • Görner, H., (2005) Effects of 4,5-dimethoxy groups on the time-resolved photoconversion of 2-nitrobenzyl alcohols and 2-nitrobenzaldehyde into nitroso derivatives. Photochem. Photobiol. Sci. 4, 822-828.
    • (2005) Photochem. Photobiol. Sci. , vol.4 , pp. 822-828
    • Görner, H.1
  • 50
    • 69649087599 scopus 로고    scopus 로고
    • Theoretical investigation of the excited states of 2-nitrobenzyl and 4,5-methylendioxy-2-nitrobenzyl caging groups
    • Schaper, K., M. Etinski, and, T. Fleig, (2009) Theoretical investigation of the excited states of 2-nitrobenzyl and 4,5-methylendioxy-2-nitrobenzyl caging groups. Photochem. Photobiol. 85, 1075-1081.
    • (2009) Photochem. Photobiol. , vol.85 , pp. 1075-1081
    • Schaper, K.1    Etinski, M.2    Fleig, T.3
  • 51
    • 37249078220 scopus 로고    scopus 로고
    • Photoprocesses of molecules with 2-nitrobenzyl protecting groups and caged organic acids
    • Bley, F., K. Schaper, and, H. Görner, (2008) Photoprocesses of molecules with 2-nitrobenzyl protecting groups and caged organic acids. Photochem. Photobiol. 84, 162-171.
    • (2008) Photochem. Photobiol. , vol.84 , pp. 162-171
    • Bley, F.1    Schaper, K.2    Görner, H.3
  • 53
    • 0033537680 scopus 로고    scopus 로고
    • Synthesis and photochemistry of a photolabile precursor of N-methyl-D-aspartate (NMDA) that is photolyzed in the microsecond time region and is suitable for chemical kinetic investigations of the NMDA receptor
    • Gee, K. R., L. Niu, K. Schaper, V. Jayaraman, and, G. P. Hess, (1999) Synthesis and photochemistry of a photolabile precursor of N-methyl-D-aspartate (NMDA) that is photolyzed in the microsecond time region and is suitable for chemical kinetic investigations of the NMDA receptor. Biochemistry 38, 3140-3147.
    • (1999) Biochemistry , vol.38 , pp. 3140-3147
    • Gee, K.R.1    Niu, L.2    Schaper, K.3    Jayaraman, V.4    Hess, G.P.5
  • 54
    • 0000351408 scopus 로고
    • Caged bioactive carboxylates-Synthesis, photolysis studies, and biological characterization of a new caged N-methyl-D-aspartic acid
    • Gee, K. R., L. Niu, K. Schaper, and, G. P. Hess, (1995) Caged bioactive carboxylates-Synthesis, photolysis studies, and biological characterization of a new caged N-methyl-D-aspartic acid. J. Org. Chem. 60, 4260-4263.
    • (1995) J. Org. Chem. , vol.60 , pp. 4260-4263
    • Gee, K.R.1    Niu, L.2    Schaper, K.3    Hess, G.P.4
  • 55
    • 0036203352 scopus 로고    scopus 로고
    • Synthesis and photophysical characterization of a new, highly hydrophilic caging group
    • Schaper, K., S. A. Madani Mobarekeh, and, C. Grewer, (2002) Synthesis and photophysical characterization of a new, highly hydrophilic caging group. Eur. J. Org. Chem. 1037-1046.
    • (2002) Eur. J. Org. Chem. , pp. 1037-1046
    • Schaper, K.1    Madani Mobarekeh, S.A.2    Grewer, C.3
  • 59
    • 0035830453 scopus 로고    scopus 로고
    • Substrate translocation kinetics of excitatory amino acid carrier 1 probed with laser-pulse photolysis of a new photolabile precursor of D-aspartic acid
    • Grewer, C., S. A. Madani Mobarekeh, N. Watzke, T. Rauen, and, K. Schaper, (2001) Substrate translocation kinetics of excitatory amino acid carrier 1 probed with laser-pulse photolysis of a new photolabile precursor of D-aspartic acid. Biochemistry 40, 232-240.
    • (2001) Biochemistry , vol.40 , pp. 232-240
    • Grewer, C.1    Madani Mobarekeh, S.A.2    Watzke, N.3    Rauen, T.4    Schaper, K.5
  • 60
    • 0031002130 scopus 로고    scopus 로고
    • Synthesis and characterization of photolabile compounds releasing noracetylcholine in the microsecond time range
    • Peng, L., J. Wirz, and, M. Goeldner, (1997) Synthesis and characterization of photolabile compounds releasing noracetylcholine in the microsecond time range. Angew. Chem. Int. Ed. 36, 398-400.
    • (1997) Angew. Chem. Int. Ed. , vol.36 , pp. 398-400
    • Peng, L.1    Wirz, J.2    Goeldner, M.3
  • 61
    • 0034899882 scopus 로고    scopus 로고
    • Photochemical reaction mechanisms of 2-nitrobenzyl compounds in solution I. 2-nitrotoluene: Thermodynamic and kinetic parameters of the aci-nitro tautomer
    • Schwörer, M., and, J. Wirz, (2001) Photochemical reaction mechanisms of 2-nitrobenzyl compounds in solution I. 2-nitrotoluene: thermodynamic and kinetic parameters of the aci-nitro tautomer. Helv. Chim. Acta 84, 1441-1458.
    • (2001) Helv. Chim. Acta , vol.84 , pp. 1441-1458
    • Schwörer, M.1    Wirz, J.2
  • 62
    • 37749040027 scopus 로고    scopus 로고
    • Studies of decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl (CNB) caged compounds
    • Corrie, J. E. T., V. R. N. Munasinghe, D. R. Trenthama, and, A. Barth, (2008) Studies of decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl (CNB) caged compounds. Photochem. Photobiol. Sci. 7, 84-97.
    • (2008) Photochem. Photobiol. Sci. , vol.7 , pp. 84-97
    • Corrie, J.E.T.1    Munasinghe, V.R.N.2    Trenthama, D.R.3    Barth, A.4
  • 63
    • 0025359827 scopus 로고
    • Photochemical manipulation of divalent-cation levels
    • Kaplan, J. H., (1990) Photochemical manipulation of divalent-cation levels. Annu. Rev. Physiol. 52, 897-914.
    • (1990) Annu. Rev. Physiol. , vol.52 , pp. 897-914
    • Kaplan, J.H.1
  • 64
    • 0031745427 scopus 로고    scopus 로고
    • Synthesis, photochemistry, and biological characterization of photolabile protecting groups for carboxylic acids and neutrotranmitters
    • In (Edited by G. Marriott). Academic Press, San Diego, London, Boston, New York, Sydney, Tokyo, Toronto, Methods Enzymol
    • Gee, K. R., B. K. Carpenter, and, G. P. Hess, (1998) Synthesis, photochemistry, and biological characterization of photolabile protecting groups for carboxylic acids and neutrotranmitters. In Caged Compounds (Edited by, G. Marriott,). Academic Press, San Diego, London, Boston, New York, Sydney, Tokyo, Toronto, Methods Enzymol. 291, 30-50.
    • (1998) Caged Compounds , vol.291 , pp. 30-50
    • Gee, K.R.1    Carpenter, B.K.2    Hess, G.P.3
  • 65
    • 0027480532 scopus 로고
    • Controlling cell chemistry with caged compounds
    • Adams, S. R., and, R. Y. Tsien, (1993) Controlling cell chemistry with caged compounds. Annu. Rev. Physiol. 55, 755-784.
    • (1993) Annu. Rev. Physiol. , vol.55 , pp. 755-784
    • Adams, S.R.1    Tsien, R.Y.2
  • 66
    • 0000107109 scopus 로고
    • Caged nucleotides and neurotransmitters
    • In (Edited by H. Morrison). John Wiley & Sons, Inc., New York, Chichester, Brisbane, Toronto, Singapore. Bioorganic Photochemistry Series
    • Corrie, J. E. T., and, D. R. Trentham, (1993) Caged nucleotides and neurotransmitters. In Biological Applications of Photochemical Switches (Edited by, H. Morrison,). John Wiley & Sons, Inc., New York, Chichester, Brisbane, Toronto, Singapore. Bioorganic Photochemistry Series, 2, 243-305.
    • (1993) Biological Applications of Photochemical Switches , vol.2 , pp. 243-305
    • Corrie, J.E.T.1    Trentham, D.R.2
  • 67
    • 0027458778 scopus 로고
    • Determination of the chemical mechanism of neurotransmitter receptor-mediated reactions by rapid chemical kinetic techniques
    • Hess, G. P., (1993) Determination of the chemical mechanism of neurotransmitter receptor-mediated reactions by rapid chemical kinetic techniques. Biochemistry 32, 989-1000.
    • (1993) Biochemistry , vol.32 , pp. 989-1000
    • Hess, G.P.1
  • 68
    • 0030767871 scopus 로고    scopus 로고
    • Caged NADP and NAD. Synthesis and characterization of functionally distinct caged compounds
    • Cohen, B. E., B. L. Stoddard, and, D. E. Koshland, (1997) Caged NADP and NAD. Synthesis and characterization of functionally distinct caged compounds. Biochemistry 36, 9035-9044.
    • (1997) Biochemistry , vol.36 , pp. 9035-9044
    • Cohen, B.E.1    Stoddard, B.L.2    Koshland, D.E.3
  • 69
    • 34748832145 scopus 로고
    • A semi-empirical theory of the electronic spectra and electronic structure of complex molecules. 2
    • Pariser, R., and, R. G. Parr, (1953) A semi-empirical theory of the electronic spectra and electronic structure of complex molecules. 2. J. Chem. Phys. 21, 767-776.
    • (1953) J. Chem. Phys. , vol.21 , pp. 767-776
    • Pariser, R.1    Parr, R.G.2
  • 70
    • 4243585088 scopus 로고
    • Chemical reactivity and concepts of charge- and frontier controlled reactions
    • Klopman, G., (1968) Chemical reactivity and concepts of charge- and frontier controlled reactions. J. Am. Chem. Soc. 90, 223-234.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 223-234
    • Klopman, G.1


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