메뉴 건너뛰기




Volumn 8, Issue 6, 2013, Pages 1303-1310

Carbofluoresceins and carborhodamines as scaffolds for high-contrast fluorogenic probes

Author keywords

[No Author keywords available]

Indexed keywords

CARBOFLURESCEIN DERIVATIVE; CARBORHODAMINE DERIVATIVE; FLUORESCEIN; RHODAMINE 110; TETRAMETHYLRHODAMINE; UNCLASSIFIED DRUG; XANTHENE;

EID: 84879769881     PISSN: 15548929     EISSN: 15548937     Source Type: Journal    
DOI: 10.1021/cb4000822     Document Type: Article
Times cited : (178)

References (50)
  • 2
    • 42449100481 scopus 로고    scopus 로고
    • Bright ideas for chemical biology
    • Lavis, L. D. and Raines, R. T. (2008) Bright ideas for chemical biology ACS Chem. Biol. 3, 142-155
    • (2008) ACS Chem. Biol. , vol.3 , pp. 142-155
    • Lavis, L.D.1    Raines, R.T.2
  • 3
    • 84870168520 scopus 로고    scopus 로고
    • Reaction-based small-molecule fluorescent probes for chemoselective bioimaging
    • Chan, J., Dodani, S. C., and Chang, C. J. (2012) Reaction-based small-molecule fluorescent probes for chemoselective bioimaging Nat. Chem. 4, 973-984
    • (2012) Nat. Chem. , vol.4 , pp. 973-984
    • Chan, J.1    Dodani, S.C.2    Chang, C.J.3
  • 5
    • 0033566587 scopus 로고    scopus 로고
    • Fluorogenic substrates based on fluorinated umbelliferones for continuous assays of phosphatases and β-galactosidases
    • Gee, K. R., Sun, W.-C., Bhalgat, M. K., Upson, R. H., Klaubert, D. H., Latham, K. A., and Haugland, R. P. (1999) Fluorogenic substrates based on fluorinated umbelliferones for continuous assays of phosphatases and β-galactosidases Anal. Biochem. 273, 41-48
    • (1999) Anal. Biochem. , vol.273 , pp. 41-48
    • Gee, K.R.1    Sun, W.-C.2    Bhalgat, M.K.3    Upson, R.H.4    Klaubert, D.H.5    Latham, K.A.6    Haugland, R.P.7
  • 6
    • 0031573401 scopus 로고    scopus 로고
    • A stable nonfluorescent derivative of resorufin for the fluorometric determination of trace hydrogen peroxide: Applications in detecting the activity of phagocyte NADPH oxidase and other oxidases
    • Zhou, M., Diwu, Z., Panchuk-Voloshina, N., and Haugland, R. P. (1997) A stable nonfluorescent derivative of resorufin for the fluorometric determination of trace hydrogen peroxide: Applications in detecting the activity of phagocyte NADPH oxidase and other oxidases Anal. Biochem. 253, 162-168
    • (1997) Anal. Biochem. , vol.253 , pp. 162-168
    • Zhou, M.1    Diwu, Z.2    Panchuk-Voloshina, N.3    Haugland, R.P.4
  • 7
    • 13644270489 scopus 로고    scopus 로고
    • Latent fluorophore based on the trimethyl lock
    • Chandran, S. S., Dickson, K. A., and Raines, R. T. (2005) Latent fluorophore based on the trimethyl lock J. Am. Chem. Soc. 127, 1652-1653
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 1652-1653
    • Chandran, S.S.1    Dickson, K.A.2    Raines, R.T.3
  • 9
    • 28444495141 scopus 로고    scopus 로고
    • Boronate-based fluorescent probes for imaging cellular hydrogen peroxide
    • Miller, E. W., Albers, A. E., Pralle, A., Isacoff, E. Y., and Chang, C. J. (2005) Boronate-based fluorescent probes for imaging cellular hydrogen peroxide J. Am. Chem. Soc. 127, 16652-16659
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 16652-16659
    • Miller, E.W.1    Albers, A.E.2    Pralle, A.3    Isacoff, E.Y.4    Chang, C.J.5
  • 10
    • 0013866506 scopus 로고
    • Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters
    • Rotman, B. and Papermaster, B. W. (1966) Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters Proc. Natl. Acad. Sci. U.S.A. 55, 134-141
    • (1966) Proc. Natl. Acad. Sci. U.S.A. , vol.55 , pp. 134-141
    • Rotman, B.1    Papermaster, B.W.2
  • 11
    • 0025740949 scopus 로고
    • Actin microfilament dynamics in locomoting cells
    • Theriot, J. A. and Mitchison, T. J. (1991) Actin microfilament dynamics in locomoting cells Nature 352, 126-131
    • (1991) Nature , vol.352 , pp. 126-131
    • Theriot, J.A.1    Mitchison, T.J.2
  • 12
    • 33947572602 scopus 로고    scopus 로고
    • Fluorogenic label for biomolecular imaging
    • Lavis, L. D., Chao, T.-Y., and Raines, R. T. (2006) Fluorogenic label for biomolecular imaging ACS Chem. Biol. 1, 252-260
    • (2006) ACS Chem. Biol. , vol.1 , pp. 252-260
    • Lavis, L.D.1    Chao, T.-Y.2    Raines, R.T.3
  • 15
    • 69249101987 scopus 로고    scopus 로고
    • Synthesis and applications of rhodamine derivatives as fluorescent probes
    • Beija, M., Afonso, C. A. M., and Martinho, J. M. G. (2009) Synthesis and applications of rhodamine derivatives as fluorescent probes Chem. Soc. Rev. 38, 2410-2433
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2410-2433
    • Beija, M.1    Afonso, C.A.M.2    Martinho, J.M.G.3
  • 16
    • 84055224080 scopus 로고    scopus 로고
    • Synthesis of rhodamines from fluoresceins using Pd-catalyzed C-N cross-coupling
    • Grimm, J. B. and Lavis, L. D. (2011) Synthesis of rhodamines from fluoresceins using Pd-catalyzed C-N cross-coupling Org. Lett. 13, 6354-6357
    • (2011) Org. Lett. , vol.13 , pp. 6354-6357
    • Grimm, J.B.1    Lavis, L.D.2
  • 18
    • 3142743939 scopus 로고    scopus 로고
    • Heteroatom substitution induced changes in excited-state photophysics and singlet oxygen generation in chalcogenoxanthylium dyes: Effect of sulfur and selenium substitutions
    • Ohulchanskyy, T. Y., Donnelly, D. J., Detty, M. R., and Prasad, P. N. (2004) Heteroatom substitution induced changes in excited-state photophysics and singlet oxygen generation in chalcogenoxanthylium dyes: Effect of sulfur and selenium substitutions J. Phys. Chem. B 108, 8668-8672
    • (2004) J. Phys. Chem. B , vol.108 , pp. 8668-8672
    • Ohulchanskyy, T.Y.1    Donnelly, D.J.2    Detty, M.R.3    Prasad, P.N.4
  • 21
  • 22
    • 79955049340 scopus 로고    scopus 로고
    • Development of a fluorescein analogue, TokyoMagenta, as a novel scaffold for fluorescence probes in red region
    • Egawa, T., Koide, Y., Hanaoka, K., Komatsu, T., Terai, T., and Nagano, T. (2011) Development of a fluorescein analogue, TokyoMagenta, as a novel scaffold for fluorescence probes in red region Chem. Commun. 47, 4162-4164
    • (2011) Chem. Commun. , vol.47 , pp. 4162-4164
    • Egawa, T.1    Koide, Y.2    Hanaoka, K.3    Komatsu, T.4    Terai, T.5    Nagano, T.6
  • 23
    • 79961096448 scopus 로고    scopus 로고
    • Evolution of Group 14 rhodamines as platforms for near-infrared fluorescence probes utilizing photoinduced electron transfer
    • Koide, Y., Urano, Y., Hanaoka, K., Terai, T., and Nagano, T. (2011) Evolution of Group 14 rhodamines as platforms for near-infrared fluorescence probes utilizing photoinduced electron transfer ACS Chem. Biol. 6, 600-608
    • (2011) ACS Chem. Biol. , vol.6 , pp. 600-608
    • Koide, Y.1    Urano, Y.2    Hanaoka, K.3    Terai, T.4    Nagano, T.5
  • 28
    • 0024336003 scopus 로고
    • Fluorescent indicators for cytosolic calcium based on rhodamine and fluorescein chromophores
    • Minta, A., Kao, J. P., and Tsien, R. Y. (1989) Fluorescent indicators for cytosolic calcium based on rhodamine and fluorescein chromophores J. Biol. Chem. 264, 8171-8178
    • (1989) J. Biol. Chem. , vol.264 , pp. 8171-8178
    • Minta, A.1    Kao, J.P.2    Tsien, R.Y.3
  • 29
    • 56449129272 scopus 로고    scopus 로고
    • Synthesis and spectroscopic properties of rosamines with cyclic amine substituents
    • Wu, L. and Burgess, K. (2008) Synthesis and spectroscopic properties of rosamines with cyclic amine substituents J. Org. Chem. 73, 8711-8718
    • (2008) J. Org. Chem. , vol.73 , pp. 8711-8718
    • Wu, L.1    Burgess, K.2
  • 32
    • 16844362313 scopus 로고    scopus 로고
    • Evolution of fluorescein as a platform for finely tunable fluorescence probes
    • Urano, Y., Kamiya, M., Kanda, K., Ueno, T., Hirose, K., and Nagano, T. (2005) Evolution of fluorescein as a platform for finely tunable fluorescence probes J. Am. Chem. Soc. 127, 4888-4894
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4888-4894
    • Urano, Y.1    Kamiya, M.2    Kanda, K.3    Ueno, T.4    Hirose, K.5    Nagano, T.6
  • 33
    • 4544311534 scopus 로고    scopus 로고
    • A LiCl-Mediated Br/Mg exchange reaction for the preparation of functionalized aryl-and heteroarylmagnesium compounds from organic bromides
    • Krasovskiy, A. and Knochel, P. (2004) A LiCl-Mediated Br/Mg exchange reaction for the preparation of functionalized aryl-and heteroarylmagnesium compounds from organic bromides Angew. Chem., Int. Ed. 43, 3333-3336
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 3333-3336
    • Krasovskiy, A.1    Knochel, P.2
  • 35
    • 0001674698 scopus 로고
    • 13C NMR study
    • 13C NMR study Tetrahedron 37, 1607-1611
    • (1981) Tetrahedron , vol.37 , pp. 1607-1611
    • Berger, S.1
  • 37
    • 50649093685 scopus 로고
    • Rhodamine dyes and related compounds. XIV. Mutual conversions of colorless and colored forms of rhodamine and rhodol
    • Ioffe, I. S. and Otten, V. F. (1965) Rhodamine dyes and related compounds. XIV. Mutual conversions of colorless and colored forms of rhodamine and rhodol Zh. Obshch. Khim. 1, 343-346
    • (1965) Zh. Obshch. Khim. , vol.1 , pp. 343-346
    • Ioffe, I.S.1    Otten, V.F.2
  • 38
    • 70349276832 scopus 로고    scopus 로고
    • Fluorogenic affinity label for the facile, rapid imaging of proteins in live cells
    • Watkins, R. W., Lavis, L. D., Kung, V. M., Los, G. V., and Raines, R. T. (2009) Fluorogenic affinity label for the facile, rapid imaging of proteins in live cells Org. Biomol. Chem. 7, 3969-3975
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 3969-3975
    • Watkins, R.W.1    Lavis, L.D.2    Kung, V.M.3    Los, G.V.4    Raines, R.T.5
  • 39
    • 0000932682 scopus 로고
    • Dielectric constant for the dioxane-water system from 20 to 35
    • Critchfield, F. E., Gibson, J. A., Jr, and Hall, J. L. (1953) Dielectric constant for the dioxane-water system from 20 to 35 J. Am. Chem. Soc. 75, 1991-1992
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 1991-1992
    • Critchfield, F.E.1    Gibson, Jr.J.A.2    Hall, J.L.3
  • 44
    • 84857577898 scopus 로고    scopus 로고
    • A caged, localizable rhodamine for superresolution microscopy
    • Banala, S., Maurel, D., Manley, S., and Johnsson, K. (2011) A caged, localizable rhodamine for superresolution microscopy ACS Chem. Biol. 7, 289-293
    • (2011) ACS Chem. Biol. , vol.7 , pp. 289-293
    • Banala, S.1    Maurel, D.2    Manley, S.3    Johnsson, K.4
  • 45
    • 15744396330 scopus 로고    scopus 로고
    • Carbocyanine dyes as efficient reversible single-molecule optical switch
    • Heilemann, M., Margeat, E., Kasper, R., Sauer, M., and Tinnefeld, P. (2005) Carbocyanine dyes as efficient reversible single-molecule optical switch J. Am. Chem. Soc. 127, 3801-3806
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3801-3806
    • Heilemann, M.1    Margeat, E.2    Kasper, R.3    Sauer, M.4    Tinnefeld, P.5
  • 48
    • 82355191588 scopus 로고    scopus 로고
    • Evaluation of fluorophores for optimal performance in localization-based super-resolution imaging
    • Dempsey, G. T., Vaughan, J. C., Chen, K. H., Bates, M., and Zhuang, X. (2011) Evaluation of fluorophores for optimal performance in localization-based super-resolution imaging Nat. Methods 8, 1027-1036
    • (2011) Nat. Methods , vol.8 , pp. 1027-1036
    • Dempsey, G.T.1    Vaughan, J.C.2    Chen, K.H.3    Bates, M.4    Zhuang, X.5
  • 50
    • 65549088576 scopus 로고    scopus 로고
    • Advances in the speed and resolution of light microscopy
    • Ji, N., Shroff, H., Zhong, H., and Betzig, E. (2008) Advances in the speed and resolution of light microscopy Curr. Opin. Neurobiol. 18, 605-616
    • (2008) Curr. Opin. Neurobiol. , vol.18 , pp. 605-616
    • Ji, N.1    Shroff, H.2    Zhong, H.3    Betzig, E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.