Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Attenuation of the Aggregation and Neurotoxicity of Amyloid-β Peptides by Catalytic PhotooxygenationTaniguchi, Atsuhiko ; Sasaki, Daisuke ; Shiohara, Azusa ; Iwatsubo, Takeshi ; Tomita, Taisuke ; Sohma, Youhei ; Kanai, MotomuAngewandte Chemie (International ed.), 2014-01, Vol.53 (5), p.1382-1385 [Periódico revisado por pares]Weinheim: WILEY-VCH VerlagTexto completo disponível |
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2 |
Material Type: Artigo
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Covalent modifier-type aggregation inhibitor of amyloid-β based on a cyclo-KLVFF motifKino, Ryuto ; Araya, Takushi ; Arai, Tadamasa ; Sohma, Youhei ; Kanai, MotomuBioorganic & medicinal chemistry letters, 2015-08, Vol.25 (15), p.2972-2975 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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3 |
Material Type: Artigo
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A Cyclic KLVFF-Derived Peptide Aggregation Inhibitor Induces the Formation of Less-Toxic Off-Pathway Amyloid-β OligomersArai, Tadamasa ; Sasaki, Daisuke ; Araya, Takushi ; Sato, Takeshi ; Sohma, Youhei ; Kanai, MotomuChembiochem : a European journal of chemical biology, 2014-11, Vol.15 (17), p.2577-2583 [Periódico revisado por pares]Weinheim: WILEY-VCH VerlagTexto completo disponível |
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4 |
Material Type: Artigo
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O-Acyl isopeptide method: development of an O-acyl isodipeptide unit for Boc SPPS and its application to the synthesis of A[beta]1-42 isopeptideYoshiya, Taku ; Uemura, Tsuyoshi ; Maruno, Takahiro ; Kubo, Shigeru ; Kiso, Yoshiaki ; Sohma, Youhei ; Kobayashi, Yuji ; Yoshizawa-Kumagaye, Kumiko ; Nishiuchi, YujiJournal of peptide science, 2014-09, Vol.20 (9), p.669-674 [Periódico revisado por pares]Bognor Regis: Wiley Subscription Services, IncTexto completo disponível |
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5 |
Material Type: Artigo
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Synthesis of chemically-tethered amyloid-β segment trimer possessing amyloidogenic propertiesShinoda, Kiyomichi ; Sohma, Youhei ; Kanai, MotomuBioorganic & medicinal chemistry letters, 2015-08, Vol.25 (15), p.2976-2979 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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6 |
Material Type: Artigo
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“Click Peptides”--Chemical Biology-Oriented Synthesis of Alzheimer's Disease-Related Amyloid β Peptide (Aβ) Analogues Based on the “O-Acyl Isopeptide Method”Sohma, Youhei ; Kiso, YoshiakiChembiochem : a European journal of chemical biology, 2006-10, Vol.7 (10), p.1549-1557 [Periódico revisado por pares]Weinheim: Wiley-VCH VerlagTexto completo disponível |
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7 |
Material Type: Artigo
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A new class of aggregation inhibitor of amyloid-β peptide based on an O-acyl isopeptideKawashima, Hiroyuki ; Sohma, Youhei ; Nakanishi, Tomoya ; Kitamura, Hitomi ; Mukai, Hidehito ; Yamashita, Masayuki ; Akaji, Kenichi ; Kiso, YoshiakiBioorganic & medicinal chemistry, 2013-11, Vol.21 (21), p.6323-6327 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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8 |
Material Type: Artigo
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Rational Design and Identification of a Non-Peptidic Aggregation Inhibitor of Amyloid-β Based on a Pharmacophore Motif Obtained from cyclo[-Lys-Leu-Val-Phe-Phe-]Arai, Tadamasa ; Araya, Takushi ; Sasaki, Daisuke ; Taniguchi, Atsuhiko ; Sato, Takeshi ; Sohma, Youhei ; Kanai, MotomuAngewandte Chemie (International ed.), 2014-07, Vol.53 (31), p.8236-8239 [Periódico revisado por pares]Weinheim: WILEY-VCH VerlagTexto completo disponível |
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9 |
Material Type: Artigo
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Development of O-acyl isopeptide methodSohma, Youhei ; Yoshiya, Taku ; Taniguchi, Atsuhiko ; Kimura, Tooru ; Hayashi, Yoshio ; Kiso, YoshiakiBiopolymers, 2007, Vol.88 (2), p.253-262 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Artigo
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Controlled Production of Amyloid β Peptide from a Photo‐Triggered, Water‐Soluble Precursor “Click PeptideTaniguchi, Atsuhiko ; Skwarczynski, Mariusz ; Sohma, Youhei ; Okada, Takuma ; Ikeda, Keisuke ; Prakash, Halan ; Mukai, Hidehito ; Hayashi , Yoshio ; Kimura, Tooru ; Hirota, Shun ; Matsuzaki, Katsumi ; Kiso, YoshiakiChembiochem : a European journal of chemical biology, 2008-12, Vol.9 (18), p.3055-3065 [Periódico revisado por pares]Weinheim: WILEY‐VCH VerlagTexto completo disponível |