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Design, synthesis, and biological activity of novel, potent, and highly selective fused pyrimidine-2-carboxamide-4-one-based matrix metalloproteinase (MMP)-13 zinc-binding inhibitors

Bioorganic & medicinal chemistry, 2016-12, Vol.24 (23), p.6149-6165

2016

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Discovery of Novel, Highly Potent, and Selective Matrix Metalloproteinase (MMP)-13 Inhibitors with a 1,2,4-Triazol-3-yl Moiety as a Zinc Binding Group Using a Structure-Based Design Approach

Journal of medicinal chemistry, 2017-01, Vol.60 (2), p.608-626

2017

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Identification of 2,6-Disubstituted 3H‑Imidazo[4,5‑b]pyridines as Therapeutic Agents for Dysferlinopathies through Phenotypic Screening on Patient-Derived Induced Pluripotent Stem Cells

Journal of medicinal chemistry, 2019-10, Vol.62 (20), p.9175-9187

2019

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Novel HDAC6 Inhibitors Increase Tubulin Acetylation and Rescue Axonal Transport of Mitochondria in a Model of Charcot–Marie–Tooth Type 2F

ACS chemical neuroscience, 2020-02, Vol.11 (3), p.258-267

2020

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Identification of 2,6-Disubstituted 3 H -Imidazo[4,5- b ]pyridines as Therapeutic Agents for Dysferlinopathies through Phenotypic Screening on Patient-Derived Induced Pluripotent Stem Cells

Journal of medicinal chemistry, 2019-10, Vol.62 (20), p.9175-9187

2019

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New Utilizations of Optically Active Homoallylamines: Highly Stereoselective Synthesis of Cyclic Guanidine and Thiourea

Heterocycles, 2005-12, Vol.66 (1), p.101

2005

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Structure-based design, synthesis, and biological evaluation of imidazo[1,2-b]pyridazine-based p38 MAP kinase inhibitors

Bioorganic & medicinal chemistry, 2018-02, Vol.26 (3), p.647-660

2018

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Structure‐Based Design, Synthesis, and Biological Evaluation of ImidazoPyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 2

ChemMedChem, 2019-12, Vol.14 (24), p.2093-2101

2019

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Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazopyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 1

ChemMedChem, 2019-05, Vol.14 (10), p.1022-1030

2019

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Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5‐b]Pyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 2

ChemMedChem, 2019-12, Vol.14 (24), p.2093-2101

2019

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Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5‐b]pyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 1

ChemMedChem, 2019-05, Vol.14 (10), p.1022-1030

2019

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Diastereoselective Barbier-Type and Palladium-Mediated Allylation of Optically Active Aldimine with Allylindium Reagents

Journal of organic chemistry, 2001-11, Vol.66 (22), p.7516-7518

2001

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Relationship between urinary tryptophan metabolites and longterm assisted circulation

Japanese Journal of Extra-Corporeal Technology, 2014, Vol.41(1), pp.11-14

2014

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Aluminum-Controlled Reactivity and Diastereoselectivity toward Radical Reactions of Optically Active Aldimines with Metallic Samarium

Journal of organic chemistry, 2001-02, Vol.66 (4), p.1283-1286

2001

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Electroencephalogram mapping in open heart surgery

Japanese journal of extra-corporeal technology, 1998, Vol.24 (2), p.30-34

KAIEDA, AKIRA

1998

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長期補助循環中の尿中トリプトファン代謝産物と炎症性ストレス反応の関係

体外循環技術, 2014, Vol.41(1), pp.11-14

2014

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Evaluation of function of leukocyte removal filter used by IDO that is an immunesuppression enzyme

Japanese Journal of Extra-Corporeal Technology, 2007/03/01, Vol.34(1), pp.4-6

2007

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Comparative study of DEHP and TOTM elution during cardiac surgery using extra corporeal circulation

Japanese Journal of Extra-Corporeal Technology, 2007, Vol.34(2), pp.87-90

2007

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Influence of cardio pulmonary bypass on the tryptophan metabolism

Japanese Journal of Extra-Corporeal Technology, 2007/03/01, Vol.34(1), pp.7-9

2007

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ChemInform Abstract: Diastereoselective Barbier-Type and Palladium-Mediated Allylation of Optically Active Aldimine with Allylindium Reagents

ChemInform, 2002-04, Vol.33 (15), p.no-no

2002

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Overview of the BioBank Japan Project: Study design and profile

Journal of epidemiology, 2017-03, Vol.27 (3), p.S2-S8

2017

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Overexpression of IL-38 protein in anticancer drug-induced lung injury and acute exacerbation of idiopathic pulmonary fibrosis

Respiratory investigation, 2017-09, Vol.55 (5), p.293-299

2017

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Grounded electrical-source airborne transient electromagnetics (GREATEM) survey of Aso Volcano, Japan

Exploration geophysics (Melbourne), 2014-03, Vol.45 (1), p.43-48

2014

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Efficient Photocyclization of Dithienylethene Dimer, Trimer, and Tetramer: Quantum Yield and Reaction Dynamics

Journal of the American Chemical Society, 2002-03, Vol.124 (9), p.2015-2024

2002

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Overview of BioBank Japan follow-up data in 32 diseases

Journal of epidemiology, 2017-03, Vol.27 (3), p.S22-S28

2017

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Design, synthesis, and biological activity of novel, potent, and highly selective fused pyrimidine-2-carboxamide-4-one-based matrix metalloproteinase (MMP)-13 zinc-binding inhibitors

Discovery of Novel, Highly Potent, and Selective Matrix Metalloproteinase (MMP)-13 Inhibitors with a 1,2,4-Triazol-3-yl Moiety as a Zinc Binding Group Using a Structure-Based Design Approach

Identification of 2,6-Disubstituted 3H‑Imidazo[4,5‑b]pyridines as Therapeutic Agents for Dysferlinopathies through Phenotypic Screening on Patient-Derived Induced Pluripotent Stem Cells

Novel HDAC6 Inhibitors Increase Tubulin Acetylation and Rescue Axonal Transport of Mitochondria in a Model of Charcot–Marie–Tooth Type 2F

Identification of 2,6-Disubstituted 3 H -Imidazo[4,5- b ]pyridines as Therapeutic Agents for Dysferlinopathies through Phenotypic Screening on Patient-Derived Induced Pluripotent Stem Cells

New Utilizations of Optically Active Homoallylamines: Highly Stereoselective Synthesis of Cyclic Guanidine and Thiourea

Structure-based design, synthesis, and biological evaluation of imidazo[1,2-b]pyridazine-based p38 MAP kinase inhibitors

Structure‐Based Design, Synthesis, and Biological Evaluation of ImidazoPyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 2

Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazopyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 1

Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5‐b]Pyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 2

Structure‐Based Design, Synthesis, and Biological Evaluation of Imidazo[4,5‐b]pyridin‐2‐one‐Based p38 MAP Kinase Inhibitors: Part 1

Diastereoselective Barbier-Type and Palladium-Mediated Allylation of Optically Active Aldimine with Allylindium Reagents

Relationship between urinary tryptophan metabolites and longterm assisted circulation

Aluminum-Controlled Reactivity and Diastereoselectivity toward Radical Reactions of Optically Active Aldimines with Metallic Samarium

Electroencephalogram mapping in open heart surgery

長期補助循環中の尿中トリプトファン代謝産物と炎症性ストレス反応の関係

Evaluation of function of leukocyte removal filter used by IDO that is an immunesuppression enzyme

Comparative study of DEHP and TOTM elution during cardiac surgery using extra corporeal circulation

Influence of cardio pulmonary bypass on the tryptophan metabolism

ChemInform Abstract: Diastereoselective Barbier-Type and Palladium-Mediated Allylation of Optically Active Aldimine with Allylindium Reagents

Overview of the BioBank Japan Project: Study design and profile

Overexpression of IL-38 protein in anticancer drug-induced lung injury and acute exacerbation of idiopathic pulmonary fibrosis

Grounded electrical-source airborne transient electromagnetics (GREATEM) survey of Aso Volcano, Japan

Efficient Photocyclization of Dithienylethene Dimer, Trimer, and Tetramer: Quantum Yield and Reaction Dynamics

Overview of BioBank Japan follow-up data in 32 diseases

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