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Volumn 19, Issue 8, 2008, Pages 1707-1718

Latent fluorophores based on a self-immolative linker strategy and suitable for protease sensing

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CELL DEATH; ENZYMES; MAMMALS; PROBES; REACTION KINETICS;

EID: 50249099209     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc8001997     Document Type: Article
Times cited : (51)

References (74)
  • 1
    • 33645970456 scopus 로고    scopus 로고
    • Progress in spectroscopic probes with cleavable active bonds
    • Chen, X., Sun, M., and Ma, H. (2006) Progress in spectroscopic probes with cleavable active bonds. Curr. Org. Chem. 10, 477-489.
    • (2006) Curr. Org. Chem , vol.10 , pp. 477-489
    • Chen, X.1    Sun, M.2    Ma, H.3
  • 2
    • 3543116602 scopus 로고    scopus 로고
    • Enzyme assays for high-throughput screening
    • Goddard, J.-P., and Reymond, J.-L. (2004) Enzyme assays for high-throughput screening. Curr. Opin. Biotechnol. 15, 314-322.
    • (2004) Curr. Opin. Biotechnol , vol.15 , pp. 314-322
    • Goddard, J.-P.1    Reymond, J.-L.2
  • 3
    • 3042737431 scopus 로고    scopus 로고
    • Recent advances in enzyme assays
    • Goddard, J. P., and Reymond, J. L. (2004) Recent advances in enzyme assays. Trends Biotechnol. 22, 363-370.
    • (2004) Trends Biotechnol , vol.22 , pp. 363-370
    • Goddard, J.P.1    Reymond, J.L.2
  • 5
    • 33947500247 scopus 로고    scopus 로고
    • Johnsson, N., and Johnsson, K. (2007) Chemical tools for biomolecular imaging. ACS Chem. Biol. 2, 31-38.
    • Johnsson, N., and Johnsson, K. (2007) Chemical tools for biomolecular imaging. ACS Chem. Biol. 2, 31-38.
  • 6
    • 36549070172 scopus 로고    scopus 로고
    • Fluorescent probes for nitric oxide and hydrogen peroxide in cell signaling
    • Miller, E. W., and Chang, C. J. (2007) Fluorescent probes for nitric oxide and hydrogen peroxide in cell signaling. Curr. Opin. Chem. Biol. 11, 620-625.
    • (2007) Curr. Opin. Chem. Biol , vol.11 , pp. 620-625
    • Miller, E.W.1    Chang, C.J.2
  • 8
    • 34250648340 scopus 로고    scopus 로고
    • Design of a practical fluorescent probe for superoxide based on protection-deprotection chemistry of fluoresceins with benzene-sulfonyl protecting groups
    • Maeda, H., Yamamoto, K., Kohno, I., Hafsi, L., Itoh, N., Nakagawa, S., Kanagawa, N., Suzuki, K., and Uno, T. (2007) Design of a practical fluorescent probe for superoxide based on protection-deprotection chemistry of fluoresceins with benzene-sulfonyl protecting groups. Chem. Eur. J. 13, 1946-1954.
    • (2007) Chem. Eur. J , vol.13 , pp. 1946-1954
    • Maeda, H.1    Yamamoto, K.2    Kohno, I.3    Hafsi, L.4    Itoh, N.5    Nakagawa, S.6    Kanagawa, N.7    Suzuki, K.8    Uno, T.9
  • 9
    • 34247887755 scopus 로고    scopus 로고
    • A phosphinate-based red fluorescent probe for imaging the superoxide radical anion generated by RAW264.7 macrophages
    • Xu, K., Liu, X., and Tang, B. (2007) A phosphinate-based red fluorescent probe for imaging the superoxide radical anion generated by RAW264.7 macrophages. ChemBioChem 8, 453-458.
    • (2007) ChemBioChem , vol.8 , pp. 453-458
    • Xu, K.1    Liu, X.2    Tang, B.3
  • 10
    • 33646505308 scopus 로고    scopus 로고
    • A highly selective fluorescent probe for the detection and imaging of peroxynitrite in living cells
    • Yang, D., Wang, H.-L., Sun, Z.-N., Chung, N.-W., and Shen, J.-G. (2006) A highly selective fluorescent probe for the detection and imaging of peroxynitrite in living cells. J. Am. Chem. Soc. 128, 6004-6005.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 6004-6005
    • Yang, D.1    Wang, H.-L.2    Sun, Z.-N.3    Chung, N.-W.4    Shen, J.-G.5
  • 11
    • 33846432398 scopus 로고    scopus 로고
    • Metal-based turn-on fluorescent probes for sensing nitric oxide
    • Lim, M. H., and Lippard, S. J. (2007) Metal-based turn-on fluorescent probes for sensing nitric oxide. Acc. Chem. Res. 40, 41-51.
    • (2007) Acc. Chem. Res , vol.40 , pp. 41-51
    • Lim, M.H.1    Lippard, S.J.2
  • 12
    • 34548249623 scopus 로고    scopus 로고
    • A highly selective fluorescence turn-on sensor for cysteine/homocysteine and its application in bioimaging
    • Zhang, M., Yu, M., Li, F., Zhu, M., Li, M., Gao, Y., Li, L., Liu, Z., Zhang, J., Zhang, D., Yi, T., and Huang, C (2007) A highly selective fluorescence turn-on sensor for cysteine/homocysteine and its application in bioimaging. J. Am. Chem. Soc. 129, 10322-10323.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 10322-10323
    • Zhang, M.1    Yu, M.2    Li, F.3    Zhu, M.4    Li, M.5    Gao, Y.6    Li, L.7    Liu, Z.8    Zhang, J.9    Zhang, D.10    Yi, T.11    Huang, C.12
  • 14
    • 34247538391 scopus 로고    scopus 로고
    • Combinatorial rosamine library and application to in vivo glutathione probe
    • Ahn, Y.-H., Lee, J.-S., and Chang, Y.-T. (2007) Combinatorial rosamine library and application to in vivo glutathione probe. J. Am. Chem. Soc. 129, 4510-4511.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 4510-4511
    • Ahn, Y.-H.1    Lee, J.-S.2    Chang, Y.-T.3
  • 15
    • 34548159473 scopus 로고    scopus 로고
    • A thiol-reactive fluorescence probe based on donor-excited photoinduced electron transfer: Key role of ortho substitution
    • Matsumoto, T., Urano, Y., Shoda, T., Kojima, H., and Nagano, T. (2007) A thiol-reactive fluorescence probe based on donor-excited photoinduced electron transfer: key role of ortho substitution. Org. Lett. 9, 3375-3377.
    • (2007) Org. Lett , vol.9 , pp. 3375-3377
    • Matsumoto, T.1    Urano, Y.2    Shoda, T.3    Kojima, H.4    Nagano, T.5
  • 16
    • 34748883933 scopus 로고    scopus 로고
    • A rhodamine-based fluorescent probe containing a Se-N bond for detecting thiols and its application in living cells
    • Tang, B., Xing, Y., Li, P., Zhang, N., Yu, F., and Yang, G. (2007) A rhodamine-based fluorescent probe containing a Se-N bond for detecting thiols and its application in living cells. J. Am. Chem. Soc. 129, 11666-11667.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 11666-11667
    • Tang, B.1    Xing, Y.2    Li, P.3    Zhang, N.4    Yu, F.5    Yang, G.6
  • 17
    • 43549112613 scopus 로고    scopus 로고
    • Fluorescence imaging of cellular glutathione using a latent rhodamine
    • Pires, M. M., and Chmielewski, J. (2008) Fluorescence imaging of cellular glutathione using a latent rhodamine. Org. Lett. 10, 837-840.
    • (2008) Org. Lett , vol.10 , pp. 837-840
    • Pires, M.M.1    Chmielewski, J.2
  • 18
    • 34547863487 scopus 로고    scopus 로고
    • Membrane permeable esterase-activated fluorescent imaging probe
    • Kim, Y., Choi, Y., Weissleder, R., and Tung, C.-H. (2007) Membrane permeable esterase-activated fluorescent imaging probe. Bioorg. Med. Chem. Lett. 17, 5054-5057.
    • (2007) Bioorg. Med. Chem. Lett , vol.17 , pp. 5054-5057
    • Kim, Y.1    Choi, Y.2    Weissleder, R.3    Tung, C.-H.4
  • 19
    • 0031571676 scopus 로고    scopus 로고
    • Fluorometric and colorimetric detection of caspase activity associated with apoptosis
    • Gurtu, V., Kain, S. R., and Zhang, G. (1997) Fluorometric and colorimetric detection of caspase activity associated with apoptosis. Anal. Biochem. 251, 98-102.
    • (1997) Anal. Biochem , vol.251 , pp. 98-102
    • Gurtu, V.1    Kain, S.R.2    Zhang, G.3
  • 20
    • 17144388653 scopus 로고    scopus 로고
    • N-DEVD-N′- morpholinecarbonyl-rhodamine 110: Novel caspase-3 fluorogenic substrates for cell-based apoptosis assay
    • and references cited therein
    • Wang, Z.-Q., Liao, J., and Diwu, Z. (2005) N-DEVD-N′- morpholinecarbonyl-rhodamine 110: novel caspase-3 fluorogenic substrates for cell-based apoptosis assay. Bioorg. Med. Chem. Lett. 15, 2335-2338 and references cited therein.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 2335-2338
    • Wang, Z.-Q.1    Liao, J.2    Diwu, Z.3
  • 21
    • 33645870980 scopus 로고    scopus 로고
    • Development of a dual fluorogenic and chromogenic dipeptidyl peptidase IV substrate
    • Ho, N.-H., Weissleder, R., and Tung, C.-H. (2006) Development of a dual fluorogenic and chromogenic dipeptidyl peptidase IV substrate. Bioorg. Med. Chem. Lett. 16, 2599-2602.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , pp. 2599-2602
    • Ho, N.-H.1    Weissleder, R.2    Tung, C.-H.3
  • 22
    • 34547154174 scopus 로고    scopus 로고
    • Selective fluorescence probes for dipeptidyl peptidase activity-fibroblast activation protein and dipeptidyl peptidase IV
    • Lai, K. S., Ho, N.-H., Cheng, J. D., and Tung, C.-H. (2007) Selective fluorescence probes for dipeptidyl peptidase activity-fibroblast activation protein and dipeptidyl peptidase IV. Bioconjugate Chem. 18, 1246-1250.
    • (2007) Bioconjugate Chem , vol.18 , pp. 1246-1250
    • Lai, K.S.1    Ho, N.-H.2    Cheng, J.D.3    Tung, C.-H.4
  • 23
    • 1642328231 scopus 로고    scopus 로고
    • In vivo imaging of β-galactosidase activity using far red fluorescent switch
    • Tung, C.-H., Zeng, Q., Shah, K., Kim, D.-E., Schellingerhout, D., and Weissleder, R. (2004) In vivo imaging of β-galactosidase activity using far red fluorescent switch. Cancer Res. 64, 1579-1583.
    • (2004) Cancer Res , vol.64 , pp. 1579-1583
    • Tung, C.-H.1    Zeng, Q.2    Shah, K.3    Kim, D.-E.4    Schellingerhout, D.5    Weissleder, R.6
  • 24
    • 42949112165 scopus 로고    scopus 로고
    • Sensitive and selective tumor imaging with novel and highly activatable fluorescence probes
    • Urano, Y. (2008) Sensitive and selective tumor imaging with novel and highly activatable fluorescence probes. Anal. Sci. 24, 51-53.
    • (2008) Anal. Sci , vol.24 , pp. 51-53
    • Urano, Y.1
  • 25
    • 0043195272 scopus 로고    scopus 로고
    • Novel fluorogenic substrates for imaging β-lactamase gene expression
    • Gao, W., Xing, B., Tsien, R. Y., and Rao, J. (2003) Novel fluorogenic substrates for imaging β-lactamase gene expression. J. Am. Chem. Soc. 125, 11146-11147.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 11146-11147
    • Gao, W.1    Xing, B.2    Tsien, R.Y.3    Rao, J.4
  • 26
    • 0037236238 scopus 로고    scopus 로고
    • Shedding light onto live molecular targets
    • Weissleder, R., and Ntziachristos, V. (2003) Shedding light onto live molecular targets. Nat. Med. 9, 123-128.
    • (2003) Nat. Med , vol.9 , pp. 123-128
    • Weissleder, R.1    Ntziachristos, V.2
  • 27
    • 0036080057 scopus 로고    scopus 로고
    • Design of selectively activated anticancer prodrugs: Elimination and cyclization strategies
    • Papot, S., Tranoy, I., Tillequin, F., Florent, J. C., and Gesson, J. P. (2002) Design of selectively activated anticancer prodrugs: elimination and cyclization strategies. Curr. Med. Chem. 2, 155-185.
    • (2002) Curr. Med. Chem , vol.2 , pp. 155-185
    • Papot, S.1    Tranoy, I.2    Tillequin, F.3    Florent, J.C.4    Gesson, J.P.5
  • 28
    • 36849072605 scopus 로고    scopus 로고
    • Cyclization-activated prodrugs
    • Gomes, P., Vale, N., and Moreira, R. (2007) Cyclization-activated prodrugs. Molecules 12, 2484-2506.
    • (2007) Molecules , vol.12 , pp. 2484-2506
    • Gomes, P.1    Vale, N.2    Moreira, R.3
  • 31
    • 13644270489 scopus 로고    scopus 로고
    • Latent fiuorophore based on the trimethyl lock
    • Chandran, S. S., Dickson, K. A., and Raines, R. T. (2005) Latent fiuorophore 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
  • 32
    • 33747181634 scopus 로고    scopus 로고
    • Latent blue and red fluorophores based on the trimethyl lock
    • Lavis, L. D., Chao, T.-Y., and Raines, R. T. (2006) Latent blue and red fluorophores based on the trimethyl lock. ChemBioChem 7, 1151-1154.
    • (2006) ChemBioChem , vol.7 , pp. 1151-1154
    • Lavis, L.D.1    Chao, T.-Y.2    Raines, R.T.3
  • 33
    • 33947572602 scopus 로고    scopus 로고
    • Lavis, L. D., Chao, T.-Y., and Raines, R. T. (2006) Fluorogenic label for biomolecular imaging. ACS Chem. Biol. 1, 252-260.
    • Lavis, L. D., Chao, T.-Y., and Raines, R. T. (2006) Fluorogenic label for biomolecular imaging. ACS Chem. Biol. 1, 252-260.
  • 34
    • 34447624702 scopus 로고    scopus 로고
    • A self-immolative reporter for β-galactosidase sensing
    • Ho, N.-H., Weissleder, R., and Tung, C.-H. (2007) A self-immolative reporter for β-galactosidase sensing. ChemBioChem 8, 560-566.
    • (2007) ChemBioChem , vol.8 , pp. 560-566
    • Ho, N.-H.1    Weissleder, R.2    Tung, C.-H.3
  • 35
    • 35148850708 scopus 로고    scopus 로고
    • Molecular probe for enzymatic activity with dual output
    • Danieli, E., and Shabat, D. (2007) Molecular probe for enzymatic activity with dual output. Bioorg. Med. Chem. 15, 7318-7324.
    • (2007) Bioorg. Med. Chem , vol.15 , pp. 7318-7324
    • Danieli, E.1    Shabat, D.2
  • 36
    • 34248340533 scopus 로고    scopus 로고
    • Fluorogenic substartes for upases, esterases, and acylases using a TIM-mechanism for signal release
    • Sicart, R., Collin, M.P., and Reymond, J.-L. (2007) Fluorogenic substartes for upases, esterases, and acylases using a TIM-mechanism for signal release. Biotechnol. J. 2, 221-231.
    • (2007) Biotechnol. J , vol.2 , pp. 221-231
    • Sicart, R.1    Collin, M.P.2    Reymond, J.-L.3
  • 37
    • 44449171547 scopus 로고    scopus 로고
    • Development of a new nonpeptidic self-immolative spacer. Application to the design of protease sensing fluorogenic probes
    • Meyer, Y., Richard, J.-A., Massonneau, M., Renard, P.-Y., and Romieu, A. (2008) Development of a new nonpeptidic self-immolative spacer. Application to the design of protease sensing fluorogenic probes. Org. Lett. 10, 1517-1520.
    • (2008) Org. Lett , vol.10 , pp. 1517-1520
    • Meyer, Y.1    Richard, J.-A.2    Massonneau, M.3    Renard, P.-Y.4    Romieu, A.5
  • 39
    • 37049120394 scopus 로고
    • Light-induced and related reactions of quinones Part III. Light-induced reactions of some monosubstituted 1,4-benzoquinones
    • Bruce, J. M., and Knowles, P. (1966) Light-induced and related reactions of quinones Part III. Light-induced reactions of some monosubstituted 1,4-benzoquinones. J. Chem. Soc., C, 1627-1634.
    • (1966) J. Chem. Soc , vol.100 , pp. 1627-1634
    • Bruce, J.M.1    Knowles, P.2
  • 40
    • 33751151068 scopus 로고
    • A new chromogenic β-galactosidase substrate: 7-β-D-galactopyranosyloxy-9,9- dirnethyl-9H-acridin-2-one
    • Corey, P. F., Trimmer, R. W., and Biddlecom, W. G. (1991) A new chromogenic β-galactosidase substrate: 7-β-D-galactopyranosyloxy-9,9- dirnethyl-9H-acridin-2-one. Angew. Chem., Int. Ed. 103, 1646-1648.
    • (1991) Angew. Chem., Int. Ed , vol.103 , pp. 1646-1648
    • Corey, P.F.1    Trimmer, R.W.2    Biddlecom, W.G.3
  • 42
    • 84889582115 scopus 로고    scopus 로고
    • NMR chemical shifts of common laboratory solvents as trace impurities
    • Gottlieb, H. E., Kotlyar, V., and Nudelman, A. (1997) NMR chemical shifts of common laboratory solvents as trace impurities. J. Org. Chem. 62, 7512-7515.
    • (1997) J. Org. Chem , vol.62 , pp. 7512-7515
    • Gottlieb, H.E.1    Kotlyar, V.2    Nudelman, A.3
  • 44
    • 0041054503 scopus 로고    scopus 로고
    • Traceless linkers - Only disappearing links in solid-phase organic synthesis
    • Bräse, S., and Dahmen, S. (2000) Traceless linkers - Only disappearing links in solid-phase organic synthesis. Chem. Eur. J. 6, 1899-1905.
    • (2000) Chem. Eur. J , vol.6 , pp. 1899-1905
    • Bräse, S.1    Dahmen, S.2
  • 45
    • 0035857545 scopus 로고    scopus 로고
    • Tracelessness unmasked: A general linker nomenclature
    • Comely, A. C., and Gibson, S. E. (2001) Tracelessness unmasked: A general linker nomenclature. Angew. Chem., Int. Ed. 40, 1012-1032.
    • (2001) Angew. Chem., Int. Ed , vol.40 , pp. 1012-1032
    • Comely, A.C.1    Gibson, S.E.2
  • 46
    • 0038198839 scopus 로고    scopus 로고
    • Recent developments in linker design and application
    • Wills, A. J., and Balasubramanian, S. (2003) Recent developments in linker design and application. Curr. Opin. Chem. Biol. 7, 346-352.
    • (2003) Curr. Opin. Chem. Biol , vol.7 , pp. 346-352
    • Wills, A.J.1    Balasubramanian, S.2
  • 47
    • 2942525368 scopus 로고    scopus 로고
    • Traceless and multifunctional linkers for the generation of small molecules on solid supports
    • Gil, C., and Bräse, S. (2004) Traceless and multifunctional linkers for the generation of small molecules on solid supports. Curr. Opin. Chem. Biol. 8, 230-237.
    • (2004) Curr. Opin. Chem. Biol , vol.8 , pp. 230-237
    • Gil, C.1    Bräse, S.2
  • 48
    • 57249083957 scopus 로고    scopus 로고
    • Enzyme-initiated domino (cascade) reactions
    • Mayer, S. F., Kroutil, W., and Kurt, F. (2001) Enzyme-initiated domino (cascade) reactions. Chem. Soc. Rev. 30, 332-339.
    • (2001) Chem. Soc. Rev , vol.30 , pp. 332-339
    • Mayer, S.F.1    Kroutil, W.2    Kurt, F.3
  • 49
    • 0034595324 scopus 로고    scopus 로고
    • An enzyme-labile safety catch linker for combinatorial synthesis on a soluble polymeric support
    • Grether, U., and Waldmann, H. (2000) An enzyme-labile safety catch linker for combinatorial synthesis on a soluble polymeric support. Angew. Chem., Int. Ed. 39, 1629-1632.
    • (2000) Angew. Chem., Int. Ed , vol.39 , pp. 1629-1632
    • Grether, U.1    Waldmann, H.2
  • 50
    • 0035793832 scopus 로고    scopus 로고
    • An enzyme-labile safety catch linker for synthesis on a soluble polymeric support
    • Grether, U., and Waldmann, H. (2001) An enzyme-labile safety catch linker for synthesis on a soluble polymeric support. Chem. Eur. J. 7, 959-971.
    • (2001) Chem. Eur. J , vol.7 , pp. 959-971
    • Grether, U.1    Waldmann, H.2
  • 51
    • 50249120275 scopus 로고    scopus 로고
    • Renard, P.-Y., Romieu, A., Richard, J.-A., and Massonneau, M. New pro-fluorescent compounds Fr. Demande (2008), FR 2910897 A1 20080704.
    • Renard, P.-Y., Romieu, A., Richard, J.-A., and Massonneau, M. New pro-fluorescent compounds Fr. Demande (2008), FR 2910897 A1 20080704.
  • 52
    • 0019453510 scopus 로고
    • A novel connector linkage applicable in prodrug design
    • Carl, P. L., Chakravarty, P. K., and Katzenellenbogen, J. A. (1981) A novel connector linkage applicable in prodrug design. J. Med. Chem. 24, 479-480.
    • (1981) J. Med. Chem , vol.24 , pp. 479-480
    • Carl, P.L.1    Chakravarty, P.K.2    Katzenellenbogen, J.A.3
  • 54
    • 33845229315 scopus 로고    scopus 로고
    • Enzymatic activation of second-generation dendritic prodrugs: Conjugation of self-immolative dendrimers with poly(ethylene glycol) via click chemistry
    • Gopin, A., Ebner, S., Attali, B., and Shabat, D. (2006) Enzymatic activation of second-generation dendritic prodrugs: conjugation of self-immolative dendrimers with poly(ethylene glycol) via click chemistry. Bioconjugate Chem. 17, 1432-1440.
    • (2006) Bioconjugate Chem , vol.17 , pp. 1432-1440
    • Gopin, A.1    Ebner, S.2    Attali, B.3    Shabat, D.4
  • 55
    • 34447498642 scopus 로고    scopus 로고
    • Controlled assembly of peptide nanotubes triggered by enzymatic activation of self-immolative dendrimers
    • Adler-Abramovich, L., Perry, R., Sagi, A., Gazit, E., and Shabat, D. (2007) Controlled assembly of peptide nanotubes triggered by enzymatic activation of self-immolative dendrimers. ChemBioChem 8, 859-862.
    • (2007) ChemBioChem , vol.8 , pp. 859-862
    • Adler-Abramovich, L.1    Perry, R.2    Sagi, A.3    Gazit, E.4    Shabat, D.5
  • 57
    • 0035498331 scopus 로고    scopus 로고
    • Enzymatic protecting group techniques
    • Kadereit, D., and Waldmann, H. (2001) Enzymatic protecting group techniques. Chem. Rev. 101, 3367-3396.
    • (2001) Chem. Rev , vol.101 , pp. 3367-3396
    • Kadereit, D.1    Waldmann, H.2
  • 58
    • 38249042851 scopus 로고
    • Two new fluorogenic substrates for the detection of penicillin-G-acylase activity
    • Scheper, T., Weiss, M., and Schuegerl, K. (1986) Two new fluorogenic substrates for the detection of penicillin-G-acylase activity. Anal. Chim. Acta 182, 203-206.
    • (1986) Anal. Chim. Acta , vol.182 , pp. 203-206
    • Scheper, T.1    Weiss, M.2    Schuegerl, K.3
  • 59
    • 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
    • Setsukinai, K.-I., Urano, Y., Kikuchi, K., Higuchi, T., and Nagano, T. (2000) 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, 2453-2457.
    • (2000) J. Chem. Soc., Perkin Trans , vol.2 , pp. 2453-2457
    • Setsukinai, K.-I.1    Urano, Y.2    Kikuchi, K.3    Higuchi, T.4    Nagano, T.5
  • 60
    • 14744280358 scopus 로고    scopus 로고
    • Terminal phosphate-labeled nucleotides with improved substrate properties for homogeneous nucleic acid assays
    • Sood, A., Kumar, S., Nampalli, S., Nelson, J. R., Macklin, J., and Fuller, C. W. (2005) Terminal phosphate-labeled nucleotides with improved substrate properties for homogeneous nucleic acid assays. J. Am. Chem. Soc. 127, 2394-2395.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 2394-2395
    • Sood, A.1    Kumar, S.2    Nampalli, S.3    Nelson, J.R.4    Macklin, J.5    Fuller, C.W.6
  • 61
    • 0036931366 scopus 로고    scopus 로고
    • Caspases: Keys in the ignition of cell death
    • Denault, J.-B., and Salvesen, G. S. (2002) Caspases: Keys in the ignition of cell death. Chem. Rev. 102, 4489-4499.
    • (2002) Chem. Rev , vol.102 , pp. 4489-4499
    • Denault, J.-B.1    Salvesen, G.S.2
  • 63
    • 0032773297 scopus 로고    scopus 로고
    • Imaging of caspase-3 activation in HeLa cells stimulated with etoposide using a novel fluorescent probe
    • Mizukami, S., Kikuchi, K., Higuchi, T., Urano, Y., Mashima, T., Tsuruo, T., and Nagano, T. (1999) Imaging of caspase-3 activation in HeLa cells stimulated with etoposide using a novel fluorescent probe. FEBS Lett. 453, 356-360.
    • (1999) FEBS Lett , vol.453 , pp. 356-360
    • Mizukami, S.1    Kikuchi, K.2    Higuchi, T.3    Urano, Y.4    Mashima, T.5    Tsuruo, T.6    Nagano, T.7
  • 64
    • 0034608386 scopus 로고    scopus 로고
    • Assessment of caspase activities in intact apoptotic thymocytes using cell-permeable fluorogenic caspase substrates
    • Komoriya, A., Packard, B. Z., Brown, M. J., Wu, M.-L., and Henkart, P. A. (2000) Assessment of caspase activities in intact apoptotic thymocytes using cell-permeable fluorogenic caspase substrates. J. Exp. Med. 191, 1819-1828.
    • (2000) J. Exp. Med , vol.191 , pp. 1819-1828
    • Komoriya, A.1    Packard, B.Z.2    Brown, M.J.3    Wu, M.-L.4    Henkart, P.A.5
  • 65
    • 0037020392 scopus 로고    scopus 로고
    • An azulene dimer as a near-infrared quencher
    • Pham, W., Weissleder, R., and Tung, C.-H. (2002) An azulene dimer as a near-infrared quencher. Angew. Chem., Int. Ed. 41, 3659-3662.
    • (2002) Angew. Chem., Int. Ed , vol.41 , pp. 3659-3662
    • Pham, W.1    Weissleder, R.2    Tung, C.-H.3
  • 66
    • 23944469298 scopus 로고    scopus 로고
    • Synthesis and characterization of a small, membrane-permeant, caspase-activatable far-red fluorescent peptide for imaging apoptosis
    • Bullok, K., and Piwnica-Worms, D. (2005) Synthesis and characterization of a small, membrane-permeant, caspase-activatable far-red fluorescent peptide for imaging apoptosis. J. Med. Chem. 48, 5404-5407.
    • (2005) J. Med. Chem , vol.48 , pp. 5404-5407
    • Bullok, K.1    Piwnica-Worms, D.2
  • 67
    • 33750494969 scopus 로고    scopus 로고
    • Aminopropargyl derivative of terpyridine-bis(methyl-enamine) tetraacetic acid chelate of europium (Eu (TMT)-AP3): A new reagent for fluorescent labelling of proteins and peptides
    • Poupart, S., Boudou, C., Peixoto, P., Massonneau, M., Renard, P.-Y., and Romieu, A. (2006) Aminopropargyl derivative of terpyridine-bis(methyl-enamine) tetraacetic acid chelate of europium (Eu (TMT)-AP3): a new reagent for fluorescent labelling of proteins and peptides. Org. Biomol. Chem. 4, 4165-4177.
    • (2006) Org. Biomol. Chem , vol.4 , pp. 4165-4177
    • Poupart, S.1    Boudou, C.2    Peixoto, P.3    Massonneau, M.4    Renard, P.-Y.5    Romieu, A.6
  • 68
    • 34047219123 scopus 로고    scopus 로고
    • Biochemical and in vivo characterization of a small, membrane-permeant, caspase-activatable far-red fluorescent peptide for imaging apoptosis
    • Bullok, K. E., Maxwell, D., Kesarwala, A. H., Gammon, S., Prior, J. L., Snow, M., Stanley, S., and Piwnica-Worms, D. (2007) Biochemical and in vivo characterization of a small, membrane-permeant, caspase-activatable far-red fluorescent peptide for imaging apoptosis. Biochemistry 46, 4055-4065.
    • (2007) Biochemistry , vol.46 , pp. 4055-4065
    • Bullok, K.E.1    Maxwell, D.2    Kesarwala, A.H.3    Gammon, S.4    Prior, J.L.5    Snow, M.6    Stanley, S.7    Piwnica-Worms, D.8
  • 69
    • 34547168899 scopus 로고    scopus 로고
    • Novel water-soluble near-infrared cyanine dyes: Synthesis, spectral properties, and use in the preparation of internally quenched fluorescent probes
    • Bouteiller, C., Clavé, G., Bernardin, A., Chipon, B., Massonneau, M., Renard, P.-Y., and Romieu, A. (2007) Novel water-soluble near-infrared cyanine dyes: synthesis, spectral properties, and use in the preparation of internally quenched fluorescent probes. Bioconjugate Chem. 18, 1303-1317.
    • (2007) Bioconjugate Chem , vol.18 , pp. 1303-1317
    • Bouteiller, C.1    Clavé, G.2    Bernardin, A.3    Chipon, B.4    Massonneau, M.5    Renard, P.-Y.6    Romieu, A.7
  • 70
    • 0242610958 scopus 로고    scopus 로고
    • DEVDase detection in intact apoptotic cells using the cell permeant fluorogenic substrate, (z-DEVD)2-cresyl violet
    • Lee, B. W., Johnson, G. L., Hed, S. A., Darzynkiewicz, Z., Talhouk, J. W., and Mehrotra, S. (2003) DEVDase detection in intact apoptotic cells using the cell permeant fluorogenic substrate, (z-DEVD)2-cresyl violet. BioTechniques 35, 1080-1085.
    • (2003) BioTechniques , vol.35 , pp. 1080-1085
    • Lee, B.W.1    Johnson, G.L.2    Hed, S.A.3    Darzynkiewicz, Z.4    Talhouk, J.W.5    Mehrotra, S.6
  • 71
    • 84985095006 scopus 로고
    • 2-(Trimethylsilyl)ethyl esters as a carboxyl protecting group; application in the synthesis of (-)-(S)-curvularin
    • Gerlach, H. (1977) 2-(Trimethylsilyl)ethyl esters as a carboxyl protecting group; application in the synthesis of (-)-(S)-curvularin. Helv. Chim. Acta 60, 3039-3044.
    • (1977) Helv. Chim. Acta , vol.60 , pp. 3039-3044
    • Gerlach, H.1
  • 72
    • 84985080215 scopus 로고
    • The 2-trimethylsilylethyl residue, a selectively cleavable carboxyl protecting group
    • Sieber, P. (1977) The 2-trimethylsilylethyl residue, a selectively cleavable carboxyl protecting group. Helv. Chim. Acta 60, 2711-2716.
    • (1977) Helv. Chim. Acta , vol.60 , pp. 2711-2716
    • Sieber, P.1
  • 74
    • 0031658737 scopus 로고    scopus 로고
    • The oxidative addition reaction between compounds of resorufin (7-hydroxy-3H-phenoxazin-3-one) and 2-mercaptoethanol
    • Kitson, T. M. (1998) The oxidative addition reaction between compounds of resorufin (7-hydroxy-3H-phenoxazin-3-one) and 2-mercaptoethanol. Bioorg. Chem. 26, 63-73.
    • (1998) Bioorg. Chem , vol.26 , pp. 63-73
    • Kitson, T.M.1


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