Search Results - "Imoto, Hiroshi"
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1
Visualizing cellular interactions with a generalized proximity reporter
Published in Proceedings of the National Academy of Sciences - PNAS (21-05-2013)“…Interactions among neighboring cells underpin many physiological processes ranging from early development to immune responses. When these interactions do not…”
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2
Discovery of Novel and Highly Selective Cyclopropane ALK Inhibitors through a Fragment-Assisted, Structure-Based Drug Design
Published in ACS omega (15-12-2020)“…Fragment screening is frequently used for hit identification. However, there was no report starting from a small fragment for the development of an anaplastic…”
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反射電子像を用いたベイナイト鋼中のマルテンサイトの選択可視化と機械学習を活用した相分率評価
Published in 鉄と鋼 (2024)“…Multi-phase steels are often used to realize a combination of high strength and toughness and/or ductility. To optimize their mechanical properties, it is…”
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4
Length of stay and cost for surgical site infection after abdominal and cardiac surgery in Japanese hospitals: multi-center surveillance
Published in Surgical infections (01-08-2012)“…This study evaluated the influence of surgical site infections (SSIs) after abdominal or cardiac surgery on the post-operative duration of hospitalization and…”
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5
Advanced carbon anode materials for lithium ion cells
Published in Journal of power sources (01-09-1999)“…Three kinds of carbon have been used for commercial cells: graphite, soft carbon and hard carbon. The difference in the structures of these three kinds of…”
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Orally Active CCR5 Antagonists as Anti-HIV-1 Agents 2: Synthesis and Biological Activities of Anilide Derivatives Containing a Pyridine N-Oxide Moiety
Published in Chemical & Pharmaceutical Bulletin (01-07-2004)“…In order to develop orally active CCR5 antagonists, we investigated 1-benzoxepine derivatives containing new polar substituents, such as phosphonate, phosphine…”
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Studies on Non-Thiazolidinedione Antidiabetic Agents. 2. Novel Oxyiminoalkanoic Acid Derivatives as Potent Glucose and Lipid Lowering Agents
Published in Chemical & pharmaceutical bulletin (01-02-2003)“…We previously reported that (Z)-2-{4-[(5-methyl-2-phenyl-1, 3-oxazol-4-yl)methoxy]benzyloxyimino}-2-(4-phenoxyphenyl)acetic acid (3) showed potent glucose and…”
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Selective Visualization of Martensite in Bainitic Steel Using Backscattered Electron Images and Phase Fraction Evaluation Using Machine Learning
Published in Tetsu to hagane (2024)“…Multi-phase steels are often used to realize a combination of high strength and toughness and/or ductility. To optimize their mechanical properties, it is…”
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Exo-Selective Diels-Alder Reaction Based on a Molecular Recognition Approach
Published in Journal of the American Chemical Society (01-12-1994)Get full text
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Studies on Non-Thiazolidinedione Antidiabetic Agents. 1. Discovery of Novel Oxyiminoacetic Acid Derivatives
Published in Chemical & pharmaceutical bulletin (01-10-2002)“…A novel series of oxyiminoacetic acid derivatives were synthesized in an effort to develop a potent antidiabetic agent, which does not contain the…”
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Destabilizing Domains Derived from the Human Estrogen Receptor
Published in Journal of the American Chemical Society (07-03-2012)“…Methods to rapidly and reversibly perturb the functions of specific proteins are desirable tools for studies of complex biological processes. We have…”
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Kinetic analysis of D-Alanine upon oral intake in humans
Published in Amino acids (14-10-2024)“…D-Alanine, a rare enantiomer of alanine, can potentially alleviate the worsening of viral infections and maintain circadian rhythm. This study aimed to analyze…”
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Studies on Non-Thiazolidinedione Antidiabetic Agents. 3. Preparation and Biological Activity of the Metabolites of TAK-559
Published in Chemical & pharmaceutical bulletin (2004)“…Preparation and biological activity of the metabolites of the potent antihyperglycemic and antihyperlipidemic agent,…”
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14
Discovery of Potent, Selective, and Brain-Penetrant 1H‑Pyrazol-5-yl‑1H‑pyrrolo[2,3‑b]pyridines as Anaplastic Lymphoma Kinase (ALK) Inhibitors
Published in Journal of medicinal chemistry (23-05-2019)“…Anaplastic lymphoma kinase (ALK), a member of the receptor tyrosine kinase family, is predominantly expressed in the brain and implicated in neuronal…”
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Clay mineralogy of a podzol developed under a Sciadopitys verticillata forest on Mt. Irazu, Shikoku mountains, southwest Japan
Published in Soil science and plant nutrition (Tokyo) (01-06-2004)“…A podzolic soil developed under a Sciadopitys verticillata forest on the side of Mt. Irazu in Shikoku mountains, Southwest Japan was investigated mainly by a…”
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Mineral composition of clay fractions and oxygen vacancies in silt-sized quartz in soils on the Ka-Etsu Plateau, Fukui, Central Japan: Possibility of eolian dust brought from northern Asia as parent material of soils
Published in Soil science and plant nutrition (Tokyo) (01-12-2005)“…Fine- to medium-textured soils are distributed on the Early Pliocene rocks and Pleistocene sandy sediments in the Ka-Etsu Plateau. The Jingaoka (JIN) soil was…”
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Discovery of a novel series of indoline carbamate and indolinylpyrimidine derivatives as potent GPR119 agonists
Published in Bioorganic & medicinal chemistry (01-03-2014)“…A series of indoline carbamate and indolinylpyrimidine derivatives was designed, synthesized, and evaluated as novel GPR119 agonists for the treatment of type…”
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Discovery of Potent, Selective, and Brain-Penetrant 1 H-Pyrazol-5-yl-1 H-pyrrolo[2,3- b]pyridines as Anaplastic Lymphoma Kinase (ALK) Inhibitors
Published in Journal of medicinal chemistry (23-05-2019)“…Anaplastic lymphoma kinase (ALK), a member of the receptor tyrosine kinase family, is predominantly expressed in the brain and implicated in neuronal…”
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A new class of non-thiazolidinedione, non-carboxylic-acid-based highly selective peroxisome proliferator-activated receptor (PPAR) γ agonists: Design and synthesis of benzylpyrazole acylsulfonamides
Published in Bioorganic & medicinal chemistry (15-01-2012)“…Herein, we describe the design, synthesis, and structure–activity relationships of novel benzylpyrazole acylsulfonamides as non-thiazolidinedione (TZD),…”
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Structure–activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ Agonists
Published in Bioorganic & medicinal chemistry (15-05-2012)“…In our search for a novel class of non-TZD, non-carboxylic acid peroxisome proliferator-activated receptor (PPAR) γ agonists, we explored alternative…”
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