Shibata A - Search Results

1

DNA templated nucleophilic aromatic substitution reactions for fluorogenic sensing of oligonucleotides.

Shibata A, Abe H, Ito M, Kondo Y, Shimizu S, Aikawa K, Ito Y. Shibata A, et al. Chem Commun (Camb). 2009 Nov 21;(43):6586-8. doi: 10.1039/b912896d. Epub 2009 Oct 5. Chem Commun (Camb). 2009. PMID: 19865658

2

Rhodamine-based fluorogenic probe for imaging biological thiol.

Shibata A, Furukawa K, Abe H, Tsuneda S, Ito Y. Shibata A, et al. Bioorg Med Chem Lett. 2008 Apr 1;18(7):2246-9. doi: 10.1016/j.bmcl.2008.03.014. Epub 2008 Mar 10. Bioorg Med Chem Lett. 2008. PMID: 18358719

3

Protein detection using oligonucleotide probes.

Shibata A, Abe H, Furukawa K, Tsuneda S, Ito Y. Shibata A, et al. Nucleic Acids Symp Ser (Oxf). 2009;(53):157-8. doi: 10.1093/nass/nrp079. Nucleic Acids Symp Ser (Oxf). 2009. PMID: 19749308

4

Reduction-triggered fluorescence probe for peptide-templated reactions.

Shibata A, Abe H, Furukawa K, Tsuneda S, Ito Y. Shibata A, et al. Chem Pharm Bull (Tokyo). 2009 Nov;57(11):1223-6. doi: 10.1248/cpb.57.1223. Chem Pharm Bull (Tokyo). 2009. PMID: 19881271 Free article.

5

Oligonucleotide-templated reactions for sensing nucleic acids.

Shibata A, Abe H, Ito Y. Shibata A, et al. Molecules. 2012 Feb 29;17(3):2446-63. doi: 10.3390/molecules17032446. Molecules. 2012. PMID: 22374329 Free PMC article. Review.

6

RNA-templated molecule release induced protein expression in bacterial cells.

Shibata A, Ito Y, Abe H. Shibata A, et al. Chem Commun (Camb). 2013 Jan 11;49(3):270-2. doi: 10.1039/c2cc37826d. Epub 2012 Nov 22. Chem Commun (Camb). 2013. PMID: 23174744

7

Very rapid DNA-templated reaction for efficient signal amplification and its steady-state kinetic analysis of the turnover cycle.

Shibata A, Uzawa T, Nakashima Y, Ito M, Nakano Y, Shuto S, Ito Y, Abe H. Shibata A, et al. J Am Chem Soc. 2013 Sep 25;135(38):14172-8. doi: 10.1021/ja404743m. Epub 2013 Sep 9. J Am Chem Soc. 2013. PMID: 24015779

8

Fluorogenic probes using 4-substituted-2-nitrobenzenesulfonyl derivatives as caging groups for the analysis of human glutathione transferase catalyzed reactions.

Shibata A, Nakano Y, Ito M, Araki M, Zhang J, Yoshida Y, Shuto S, Mannervik B, Morgenstern R, Ito Y, Abe H. Shibata A, et al. Analyst. 2013 Nov 12;138(24):7326-30. doi: 10.1039/c3an01339a. Analyst. 2013. PMID: 24151635

9

Characterization of a new fluorogenic substrate for microsomal glutathione transferase 1.

Alander J, Johansson K, Heuser VD, Farebo H, Järvliden J, Abe H, Shibata A, Ito M, Ito Y, Morgenstern R. Alander J, et al. Among authors: shibata a. Anal Biochem. 2009 Jul 1;390(1):52-6. doi: 10.1016/j.ab.2009.03.046. Epub 2009 Apr 5. Anal Biochem. 2009. PMID: 19348782

A new thiol-reactive electrophilic, disubstituted rhodamine-based fluorogenic probe (bis-2,4-dinitrobenzenesulfonyl rhodamine [BDR]) with very high quantum yield was synthesized and described recently [A. ...In addition, the activity could be increased by thiol reag …

A new thiol-reactive electrophilic, disubstituted rhodamine-based fluorogenic probe (bis-2,4-dinitrobenzenesulfonyl rhodamine [BDR]) …

10

Synthesis and characterization of a series of highly fluorogenic substrates for glutathione transferases, a general strategy.

Zhang J, Shibata A, Ito M, Shuto S, Ito Y, Mannervik B, Abe H, Morgenstern R. Zhang J, et al. Among authors: shibata a. J Am Chem Soc. 2011 Sep 7;133(35):14109-19. doi: 10.1021/ja205500y. Epub 2011 Aug 15. J Am Chem Soc. 2011. PMID: 21786801

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