J. Morimoto

发表

Structural basis for potent inhibition of SIRT2 deacetylase by a macrocyclic peptide inducing dynamic structural change.

H. Nishimasu, O. Nureki, I. Komuro, 2014, Structure.

Per-residue Program of Multiple Backbone Dihedral Angles of β-Peptoids via Backbone Substitutions.

K. Tsumoto, D. Kuroda, S. Nagatoishi, 2020, Journal of the American Chemical Society.

Flexizymes: their evolutionary history and the origin of catalytic function.

Yuuki Hayashi, H. Suga, K. Iwasaki, 2011, Accounts of chemical research.

Structure-based relaxation analysis reveals C-terminal [1-13C]glycine-d2 in peptides has long spin-lattice relaxation time that is applicable to in vivo hyperpolarized magnetic resonance studies

H. Nonaka, M. Matsuo, Y. Takakusagi, 2022 .

In vitro selection of anti-Akt2 thioether-macrocyclic peptides leading to isoform-selective inhibitors.

Yuuki Hayashi, H. Suga, J. Morimoto, 2012, ACS chemical biology.

Discovery of Phosphorylated Peripherin as a Major Humoral Autoantigen in Type 1 Diabetes Mellitus.

Sydney L. Stoops, T. Kodadek, Eric Koesema, 2016, Cell chemical biology.

Reliable diagnosis of murine type 1 diabetes using a panel of autoantigens and "antigen surrogates" mounted onto a liquid array.

T. Kodadek, Todd M Doran, Scott Simanski, 2015, Molecular bioSystems.

A Peptoid with Extended Shape in Water.

K. Tsumoto, S. Nagatoishi, S. Sando, 2019, Journal of the American Chemical Society.

Isolation of a peptide containing d-amino acid residues that inhibits the α-helix-mediated p53-MDM2 interaction from a one-bead one-compound library.

S. Sando, J. Morimoto, Yuki Hosono, 2018, Bioorganic & medicinal chemistry letters.

Discovery of macrocyclic peptides armed with a mechanism-based warhead: isoform-selective inhibition of human deacetylase SIRT2.

Yuuki Hayashi, H. Suga, J. Morimoto, 2012, Angewandte Chemie.

Amide-to-Ester Substitution Improves Membrane Permeability of a Cyclic Peptide Without Altering Its Three-Dimensional Structure

Matthew R. Naylor, Chad E. Townsend, Hsiau-Wei Lee, 2020 .

Synthesis of a large library of macrocyclic peptides containing multiple and diverse N-alkylated residues.

T. Kodadek, J. Morimoto, 2015, Molecular bioSystems.

A Peptoid with Extended Shape in Water.

K. Tsumoto, S. Nagatoishi, S. Sando, 2019, Journal of the American Chemical Society.

Ribosomal synthesis of bicyclic peptides via two orthogonal inter-side-chain reactions.

Hiroshi Murakami, Hiroaki Suga, H. Murakami, 2008, Journal of the American Chemical Society.

Solid-Phase Synthesis of β-Peptoids with Chiral Backbone Substituents Using Reductive Amination.

S. Sando, J. Morimoto, Yasuhiro Fukuda, 2017, Organic letters.

Shapes of seed including well-developed zygotic embryo in polyembryonic Citrus species/cultivars.

J. Morimoto, S. Nakagawa, E. Yuda, 1990 .

Dextran as a Generally Applicable Multivalent Scaffold for Improving Immunoglobulin-Binding Affinities of Peptide and Peptidomimetic Ligands

T. Kodadek, S. Kenrick, J. Morimoto, 2014, Bioconjugate chemistry.

Targeting Stereotyped B Cell Receptors from Chronic Lymphocytic Leukemia Patients with Synthetic Antigen Surrogates*

T. Kodadek, N. Chiorazzi, Haiyong Peng, 2016, The Journal of Biological Chemistry.

Peptoid-based reprogrammable template for cell-permeable inhibitors of protein–protein interactions

K. Tsumoto, S. Sando, J. Morimoto, 2021, Chemical science.

Recognition of antigen-specific B-cell receptors from chronic lymphocytic leukemia patients by synthetic antigen surrogates.

T. Kodadek, N. Chiorazzi, Haiyong Peng, 2014, Chemistry & biology.

Amide-to-ester substitution as a stable alternative to N-methylation for increasing membrane permeability in cyclic peptides

Matthew R. Naylor, Chad E. Townsend, Hsiau-Wei Lee, 2023, Nature Communications.

Acid citrus cultivars related to the Yuzu (Citrus junos Sieb. ex Tanaka) in Japan

J. Morimoto, T. Taninaka, N. Otoi, 1982 .

Each side chain of cyclosporin A is not essential for high passive permeability across lipid bilayers

H. Noji, S. Sando, K. Tabata, 2023, RSC advances.

Structural basis for potent inhibition of SIRT2 deacetylase by a macrocyclic peptide inducing dynamic structural change.

H. Nishimasu, O. Nureki, I. Komuro, 2014, Structure.

Discovery of macrocyclic peptides armed with a mechanism-based warhead: isoform-selective inhibition of human deacetylase SIRT2.

Yuuki Hayashi, H. Suga, J. Morimoto, 2012, Angewandte Chemie.

Bottom-up design of peptide nanoshapes in water using oligomers of N -methyl- L / D -alanine

K. Yonekura, S. Maki-Yonekura, S. Sando, 2022 .

Residue-based program of a β-peptoid twisted strand shape via a cyclopentane constraint.

K. Tsumoto, K. Umezawa, S. Sando, 2022, Organic & biomolecular chemistry.

Oligo(N-methylalanine) as a Peptide-Based Molecular Scaffold with a Minimal Structure and High Density of Functionalizable Sites.

K. Tsumoto, S. Sando, K. Takeuchi, 2022, Angewandte Chemie.

Peptoids with Substituents on the Backbone Carbons as Conformationally Constrained Synthetic Oligoamides

S. Sando, J. Morimoto, 2020, Journal of Synthetic Organic Chemistry, Japan.

Click3D: Click reaction across deep tissues for whole-organ 3D fluorescence imaging

Shimpei I. Kubota, J. Morimoto, Yutaro Saito, 2024, Science advances.

A parallel permeability assay of peptides across artificial membranes and cell monolayers using a fluorogenic reaction.

S. Sando, J. Morimoto, T. Ono, 2019, Organic & biomolecular chemistry.