Atsushi Kato

Professor and Director

University of Toyama

Japan

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About

Atsushi Kato is a Professor and Director at the University of Toyama, Japan. His research areas include the synthesis and evaluation of iminosugars and their derivatives for applications in glycosidase inhibition and cancer therapy. His recent articles focus on topics such as palladium-catalyzed reactions, structural diversity in chemicals, and the biological implications of iminosugars in plant glycobiology.

Articles (20)

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2025

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2025

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2025

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2025

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2025

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2025

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

Collaborators (11)

Michela Simone

Lecturer in Medicinal Chemistry and Chemical Biology

Newcastle University

AUSTRALIA

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isabelle gillaizeau

Full Professor

Université d'Orléans

FRANCE

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Charles Gauthier

Full Professor

Institut national de la recherche scientifique

CANADA

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Jérôme MARROT

Institut Lavoisier de Versailles

FRANCE

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Stephen Pyne

Senior Professor

University of Wollongong

AUSTRALIA

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Yves Blériot

University of Poitiers

FRANCE

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Farnusch Kaschani

Head of Analytics Core Facility Essen

Universität Duisburg-Essen

GERMANY

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David Gueyrard

Professor

Université Claude Bernard Lyon 1 Faculté des Sciences et Technologies

FRANCE

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Nadege Lubin-Germain

Professor

Université de Cergy-Pontoise - Site de Neuville

FRANCE

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Nobutada Tanaka

Professor

Kitasato University

JAPAN

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Pierre Buscaill

Lecturer in Plant Sciences

University of Bristol

UNITED KINGDOM

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Atsushi Kato

Research Interests

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About

Articles (20)

Addition of Lithiated 1,3-Dithiane and Nitronate to Sugar-Derived Imines: Synthesis of Homoiminosugars and Pipecolic Acid Analogues

Introduction of Structural Diversity at the C2 Position of Unsaturated Iminosugars through Palladium‐Catalyzed Cross‐Coupling Reactions

Borylated Five-Membered Ring Iminosugars: Synthesis, Spectroscopic Analysis, and Biological Evaluation for Glycosidase Inhibition and Anticancer Properties for Application in Boron Neutron Capture Therapy (BNCT)—Part 1

Bacterial pathogen deploys the iminosugar glycosyrin to manipulate plant glycobiology

C-2 fluorinated castanospermines as potent and specific α-glucosidase inhibitors: synthesis and structure–activity relationship study

C-2 fluorinated castanospermines as potent and specific α-glucosidase inhibitors: synthesis and structure–activity relationship study

Enantiomeric C-6 fluorinated swainsonine derivatives as highly selective and potent inhibitors of α-mannosidase and α-l-rhamnosidase: Design, synthesis and structure-activity relationship study

Thioarylation of 6‐Amino‐2,3,6‐trideoxy‐d‐manno‐oct‐2‐ulosonic Acid (IminoKdo): Access to 3,6‐Disubstituted Picolinates and Mechanistic Insights

Design and synthesis of 6-C-alkyl-DMDP type nanomolar inhibitors of β-galactosidase and β-glucosidase based on broussonetine S and related derivatives

Synthesis of 8-epi-l-swainsonine, related C6 alkylated derivatives and their α-l-rhamnosidase inhibition

Synthesis of the Purported Structure of Glyphaeaside C and Proposed Revisions to the Structures of the Glyphaeaside Alkaloids

Design and Pharmacological Chaperone Effects of N-(4′-Phenylbutyl)-DAB Derivatives Targeting the Lipophilic Pocket of Lysosomal Acid α-Glucosidase

Evaluation of nonnatural L-iminosugar C,C-glycosides, a new class of C-branched iminosugars, as glycosidase inhibitors

Nanomolar β-glucosidase and β-galactosidase inhibition by enantiomeric α-1-C-alkyl-1,4-dideoxy-1,4-imino-arabinitol derivatives

Design and synthesis of iso-allo-DNJ and l-isoDALDP derivatives: pursuit of potent and selective inhibitors of α-glucosidase

Design, synthesis and glycosidase inhibition of DAB derivatives with C-4 peptide and dipeptide branches

Borylated 2,3,4,5-Tetrachlorophthalimide and Their 2,3,4,5-Tetrachlorobenzamide Analogues: Synthesis, Their Glycosidase Inhibition and Anticancer Properties in View to Boron Neutron Capture Therapy

C-6 fluorinated casuarines as highly potent and selective amyloglucosidase inhibitors: Synthesis and structure-activity relationship study

trans, trans-2-C-Aryl-3,4-dihydroxypyrrolidines as potent and selective β-glucosidase inhibitors: Pharmacological chaperones for Gaucher disease

Diastereoselective Synthesis, Glycosidase Inhibition, and Docking Study of C-7-Fluorinated Casuarine and Australine Derivatives

Collaborators (11)

Michela Simone

isabelle gillaizeau

Charles Gauthier

Jérôme MARROT

Stephen Pyne

Yves Blériot

Farnusch Kaschani

David Gueyrard

Nadege Lubin-Germain

Nobutada Tanaka

Pierre Buscaill

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