Year |
Citation |
Score |
2020 |
Koboku S, Yanagi M, Funato A, Suzuki A, Saito Y. 2-Ethynylnaphthalene-modified 8-aza-3,7-dideaza-2′-deoxyadenosine derivative discriminates thymine in target DNA via changes in the fluorescence wavelength Tetrahedron Letters. 61: 151841. DOI: 10.1016/J.Tetlet.2020.151841 |
0.375 |
|
2019 |
Takeda T, Yanagi M, Suzuki A, Katoh R, Saito Y. Synthesis of ethynylpyrene-modified 3-deaza-2′-deoxyguanosines as environmentally sensitive fluorescent nucleosides: Target DNA-sequence detection via changes in the fluorescence wavelength Tetrahedron Letters. 60: 825-830. DOI: 10.1016/J.Tetlet.2019.02.002 |
0.398 |
|
2018 |
Yanagi M, Suzuki A, Hudson RHE, Saito Y. A fluorescent 3,7-bis-(naphthalen-1-ylethynylated)-2'-deoxyadenosine analogue reports thymidine in complementary DNA by a large emission Stokes shift. Organic & Biomolecular Chemistry. PMID 29417128 DOI: 10.1039/C8Ob00062J |
0.399 |
|
2018 |
Saito Y, Hudson RHE. Base-modified fluorescent purine nucleosides and nucleotides for use in oligonucleotide probes Journal of Photochemistry and Photobiology C-Photochemistry Reviews. 36: 48-73. DOI: 10.1016/J.Jphotochemrev.2018.07.001 |
0.39 |
|
2017 |
Suzuki A, Yanagi M, Takeda T, Hudson RHE, Saito Y. The fluorescently responsive 3-(naphthalen-1-ylethynyl)-3-deaza-2'-deoxyguanosine discriminates cytidine via the DNA minor groove. Organic & Biomolecular Chemistry. PMID 28880042 DOI: 10.1039/C7Ob01931A |
0.384 |
|
2017 |
Yamauchi T, Takeda T, Yanagi M, Takahashi N, Suzuki A, Saito Y. C2-substituted 8-aza-7-deaza-2'-deoxyadenosines as environmentally sensitive fluorescent nucleosides for discriminating apurinic/apyrimidinic sites in DNA duplex Tetrahedron Letters. 58: 117-120. DOI: 10.1016/J.Tetlet.2016.11.029 |
0.36 |
|
2016 |
Siraiwa S, Suzuki A, Katoh R, Saito Y. Design and synthesis of a novel fluorescent benzo[g]imidazo[4,5-c]quinoline nucleoside for monitoring base-pair-induced protonation with cytosine: distinguishing cytosine via changes in the intensity and wavelength of fluorescence. Organic & Biomolecular Chemistry. PMID 27044927 DOI: 10.1039/C6Ob00494F |
0.379 |
|
2015 |
Suzuki A, Kozakai R, Aso T, Saito I, Takeda T, Saito Y. Design and synthesis of environmentally sensitive fluorescent 2-naphthylethynylated 2'-deoxyadenosines: Detection of target DNA via changes in fluorescence intensity and wavelength. Bioorganic & Medicinal Chemistry Letters. PMID 26627578 DOI: 10.1016/J.Bmcl.2015.11.037 |
0.406 |
|
2015 |
Aso T, Saito K, Suzuki A, Saito Y. Synthesis and photophysical properties of pyrene-labeled 3-deaza-2'-deoxyadenosines comprising a non-π-conjugated linker: fluorescence quenching-based oligodeoxynucleotide probes for thymine identification. Organic & Biomolecular Chemistry. 13: 10540-7. PMID 26338764 DOI: 10.1039/C5Ob01605C |
0.388 |
|
2015 |
Suzuki A, Saito M, Katoh R, Saito Y. Synthesis of 8-aza-3,7-dideaza-2'-deoxyadenosines possessing a new adenosine skeleton as an environmentally sensitive fluorescent nucleoside for monitoring the DNA minor groove. Organic & Biomolecular Chemistry. PMID 26065387 DOI: 10.1039/C5Ob00862J |
0.406 |
|
2015 |
Saito Y, Suzuki A, Yamauchi T, Saito I. Design and synthesis of 7-naphthyl-8-aza-7-deaza-2′-deoxyadenosines as environmentally sensitive fluorescent nucleosides Tetrahedron Letters. 56: 3034-3038. DOI: 10.1016/J.Tetlet.2014.10.116 |
0.405 |
|
2014 |
Suzuki A, Yanaba T, Saito I, Saito Y. Molecular design of an environmentally sensitive fluorescent nucleoside, 3-deaza-2'-deoxyadenosine derivative: distinguishing thymine by probing the DNA minor groove. Chembiochem : a European Journal of Chemical Biology. 15: 1638-44. PMID 25044623 DOI: 10.1002/Cbic.201402078 |
0.395 |
|
2014 |
Suzuki A, Nemoto N, Saito I, Saito Y. Design of an environmentally sensitive fluorescent 8-aza-7-deaza-2'-deoxyadenosine derivative with dual fluorescence for the specific detection of thymine. Organic & Biomolecular Chemistry. 12: 660-6. PMID 24296951 DOI: 10.1039/C3Ob41757C |
0.397 |
|
2014 |
Suzuki A, Yanaba T, Saito I, Saito Y. Inside Cover: Molecular Design of an Environmentally Sensitive Fluorescent Nucleoside, 3‐Deaza‐2′‐Deoxyadenosine Derivative: Distinguishing Thymine by Probing the DNA Minor Groove (ChemBioChem 11/2014) Chembiochem. 15: 1530-1530. DOI: 10.1002/Cbic.201490037 |
0.372 |
|
2013 |
Saito Y, Suzuki A, Okada Y, Yamasaka Y, Nemoto N, Saito I. An environmentally sensitive fluorescent purine nucleoside that changes emission wavelength upon hybridization. Chemical Communications (Cambridge, England). 49: 5684-6. PMID 23685520 DOI: 10.1039/C3Cc42605J |
0.375 |
|
2013 |
Suzuki A, Takahashi N, Okada Y, Saito I, Nemoto N, Saito Y. Naphthalene-based environmentally sensitive fluorescent 8-substituted 2'-deoxyadenosines: application to DNA detection. Bioorganic & Medicinal Chemistry Letters. 23: 886-92. PMID 23273411 DOI: 10.1016/J.Bmcl.2012.11.029 |
0.382 |
|
2013 |
Suzuki A, Kimura K, Ishioroshi S, Saito I, Nemoto N, Saito Y. Synthesis of solvatofluorochromic 7-arylethynylated 7-deaza-2′-deoxyadenosine derivatives: application to the design of environmentally sensitive fluorescent probes forming stable DNA duplexes Tetrahedron Letters. 54: 2348-2352. DOI: 10.1016/J.Tetlet.2013.02.063 |
0.389 |
|
2012 |
Bag SS, Heemstra JM, Saito Y, Chenoweth DM. Expansion of the genetic alphabet: unnatural nucleobases and their applications. Journal of Nucleic Acids. 2012: 718582. PMID 23316342 DOI: 10.1155/2012/718582 |
0.303 |
|
2012 |
Tanaka M, Oguma K, Saito Y, Saito I. Enhancement of fluorescence quenching and exciplex formation in DNA major groove by double incorporation of modified fluorescent deoxyuridines. Bioorganic & Medicinal Chemistry Letters. 22: 4103-5. PMID 22578464 DOI: 10.1016/J.Bmcl.2012.04.067 |
0.391 |
|
2012 |
Saito Y, Kugenuma K, Tanaka M, Suzuki A, Saito I. Fluorometric detection of adenine in target DNA by exciplex formation with fluorescent 8-arylethynylated deoxyguanosine. Bioorganic & Medicinal Chemistry Letters. 22: 3723-6. PMID 22543030 DOI: 10.1016/J.Bmcl.2012.04.011 |
0.397 |
|
2012 |
Saito Y, Miyamoto S, Suzuki A, Matsumoto K, Ishihara T, Saito I. Fluorescent nucleosides with 'on-off' switching function, pH-responsive fluorescent uridine derivatives. Bioorganic & Medicinal Chemistry Letters. 22: 2753-6. PMID 22444678 DOI: 10.1016/J.Bmcl.2012.02.092 |
0.327 |
|
2011 |
Tanaka M, Kozakai R, Saito Y, Saito I. Stabilization of DNA duplex by 2-substituted adenine as a minor groove modifier. Bioorganic & Medicinal Chemistry Letters. 21: 7021-4. PMID 22014545 DOI: 10.1016/J.Bmcl.2011.09.104 |
0.315 |
|
2011 |
Matsumoto K, Takahashi N, Suzuki A, Morii T, Saito Y, Saito I. Design and synthesis of highly solvatochromic fluorescent 2'-deoxyguanosine and 2'-deoxyadenosine analogs. Bioorganic & Medicinal Chemistry Letters. 21: 1275-8. PMID 21273064 DOI: 10.1016/J.Bmcl.2010.11.129 |
0.391 |
|
2011 |
Saito Y, Suzuki A, Ishioroshi S, Saito I. Synthesis and photophysical properties of novel push–pull-type solvatochromic 7-deaza-2′-deoxypurine nucleosides Tetrahedron Letters. 52: 4726-4729. DOI: 10.1016/J.Tetlet.2011.06.089 |
0.387 |
|
2011 |
Saito Y, Shinohara Y, Ishioroshi S, Suzuki A, Tanaka M, Saito I. Synthesis of environmentally sensitive 2′-deoxyguanosine containing solvatochromic pyrene fluorophore Tetrahedron Letters. 52: 2359-2361. DOI: 10.1016/J.Tetlet.2011.02.088 |
0.4 |
|
2011 |
Saito Y, Koda M, Shinohara Y, Saito I. Synthesis and photophysical properties of 8-arylbutadienyl 2′-deoxyguanosines Tetrahedron Letters. 52: 491-494. DOI: 10.1016/J.Tetlet.2010.11.053 |
0.36 |
|
2010 |
Bag SS, Kundu R, Matsumoto K, Saito Y, Saito I. Singly and doubly labeled base-discriminating fluorescent oligonucleotide probes containing oxo-pyrene chromophore. Bioorganic & Medicinal Chemistry Letters. 20: 3227-30. PMID 20452214 DOI: 10.1016/J.Bmcl.2010.04.063 |
0.383 |
|
2010 |
Shinohara Y, Matsumoto K, Kugenuma K, Morii T, Saito Y, Saito I. Design of environmentally sensitive fluorescent 2'-deoxyguanosine containing arylethynyl moieties: distinction of thymine base by base-discriminating fluorescent (BDF) probe. Bioorganic & Medicinal Chemistry Letters. 20: 2817-20. PMID 20363628 DOI: 10.1016/J.Bmcl.2010.03.055 |
0.396 |
|
2010 |
Yoshida Y, Niwa K, Yamada K, Tokeshi M, Baba Y, Saito Y, Okamoto A, Saito I. A Probe Containing Two Base-discriminating Fluorescent (BDF) Nucleosides for SNP Typing Chemistry Letters. 39: 116-117. DOI: 10.1246/Cl.2010.116 |
0.315 |
|
2010 |
Saito Y, Suzuki A, Imai K, Nemoto N, Saito I. Synthesis of novel push–pull-type solvatochromic 2′-deoxyguanosine derivatives with longer wavelength emission Tetrahedron Letters. 51: 2606-2609. DOI: 10.1016/J.Tetlet.2010.03.012 |
0.365 |
|
2009 |
Matsumoto K, Shinohara Y, Bag SS, Takeuchi Y, Morii T, Saito Y, Saito I. Pyrene-labeled deoxyguanosine as a fluorescence sensor to discriminate single and double stranded DNA structures: design of ends free molecular beacons. Bioorganic & Medicinal Chemistry Letters. 19: 6392-5. PMID 19828314 DOI: 10.1016/J.Bmcl.2009.09.060 |
0.375 |
|
2009 |
Saito Y, Matsumoto K, Takeuchi Y, Bag SS, Kodate S, Morii T, Saito I. Fluorescence switching of photochromic vinylpyrene-substituted 2′-deoxyguanosine Tetrahedron Letters. 50: 1403-1406. DOI: 10.1016/J.Tetlet.2009.01.029 |
0.345 |
|
2008 |
Saito Y, Motegi K, Bag SS, Saito I. Anthracene based base-discriminating fluorescent oligonucleotide probes for SNPs typing: synthesis and photophysical properties. Bioorganic & Medicinal Chemistry. 16: 107-13. PMID 16890446 DOI: 10.1016/J.Bmc.2006.07.025 |
0.397 |
|
2008 |
Saito Y, Matsumoto K, Bag SS, Ogasawara S, Fujimoto K, Hanawa K, Saito I. C8-alkynyl- and alkylamino substituted 2′-deoxyguanosines: a universal linker for nucleic acids modification Tetrahedron. 64: 3578-3588. DOI: 10.1016/J.Tet.2008.01.091 |
0.302 |
|
2007 |
Saito Y, Bag SS, Kusakabe Y, Nagai C, Matsumoto K, Mizuno E, Kodate S, Suzuka I, Saito I. Dual-labeled oligonucleotide probe for sensing adenosine via FRET: a novel alternative to SNPs genotyping. Chemical Communications (Cambridge, England). 2133-5. PMID 17520113 DOI: 10.1039/B618465K |
0.365 |
|
2006 |
Bag SS, Saito Y, Hanawa K, Kodate S, Suzuka I, Saito I. Intelligent fluorescent nucleoside in sensing cytosine base: importance of hydrophobic nature of perylene fluorophore. Bioorganic & Medicinal Chemistry Letters. 16: 6338-41. PMID 17035014 DOI: 10.1016/J.Bmcl.2006.09.039 |
0.377 |
|
2006 |
Saito I, Saito Y, Hanawa K, Hayashi K, Motegi K, Bag SS, Dohno C, Ichiba T, Tainaka K, Okamoto A. Highly selective fluorescent nucleobases for designing base-discriminating fluorescent probes Pure and Applied Chemistry. 78: 2305-2312. DOI: 10.1351/Pac200678122305 |
0.363 |
|
2006 |
Saito Y, Hanawa K, Kawasaki N, Bag SS, Saito I. Acridone-labeled Base-discriminating Fluorescence (BDF) Nucleoside: Synthesis and Their Photophysical Properties Chemistry Letters. 35: 1182-1183. DOI: 10.1246/Cl.2006.1182 |
0.378 |
|
2005 |
Saito I, Saito Y, Okamoto A, Ichiba T, Kanatani K, Tainaka K. Design of highly selective fluorescent nucleobases for SNP typing: Base-discriminating fluorescent (BDF) probe Collection of Czechoslovak Chemical Communications. 7: 57-64. DOI: 10.1135/Css200507057 |
0.354 |
|
2005 |
Saito Y, Hanawa K, Motegi K, Omoto K, Okamoto A, Saito I. Synthesis and properties of purine-type base-discriminating fluorescent (BDF) nucleosides: distinction of thymine by fluorescence-labeled deoxyadenosine derivatives Tetrahedron Letters. 46: 7605-7608. DOI: 10.1016/J.Tetlet.2005.08.157 |
0.401 |
|
2005 |
Saito I, Miyauchi Y, Saito Y, Fujimoto K. Template-directed photoreversible ligation of DNA via 7-carboxyvinyl-7-deaza-2'-deoxyadenosine Tetrahedron Letters. 46: 97-99. DOI: 10.1016/J.Tetlet.2004.11.019 |
0.31 |
|
2005 |
Okamoto A, Saito Y, Saito I. Design of base-discriminating fluorescent nucleosides Journal of Photochemistry and Photobiology C-Photochemistry Reviews. 6: 108-122. DOI: 10.1016/J.Jphotochemrev.2005.07.002 |
0.376 |
|
2004 |
Saito Y, Miyauchi Y, Okamoto A, Saito I. Base-discriminating fluorescent (BDF) nucleoside: distinction of thymine by fluorescence quenching. Chemical Communications (Cambridge, England). 1704-5. PMID 15278146 DOI: 10.1039/B405832A |
0.392 |
|
2004 |
Saito Y, Miyauchi Y, Okamoto A, Saito I. Synthesis and properties of novel base-discriminating fluorescent (BDF) nucleosides: a highly polarity-sensitive fluorophore for SNP typing Tetrahedron Letters. 45: 7827-7831. DOI: 10.1016/J.Tetlet.2004.09.003 |
0.377 |
|
2004 |
Okamoto A, Kanatani K, Ochi Y, Saito Y, Saito I. A novel fluorescent guanine derivative distinguishable of three structures, single strand, duplex, and quadruplex Tetrahedron Letters. 45: 6059-6062. DOI: 10.1016/J.Tetlet.2004.05.136 |
0.378 |
|
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