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TADF activation by solvent freezing: The role of nonradiative triplet decay and spin-orbit coupling in carbazole benzonitrile derivatives

Synthetic metals, 2019-06, Vol.252, p.62-68

2019

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Characteristics and gene cloning of phospholipase D of the psychrophile, Shewanella sp

Bioscience, biotechnology, and biochemistry, 2007-10, Vol.71 (10)

2007

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Secondary closure of neodymium:YAG laser posterior capsulotomy

Journal of cataract and refractive surgery, 2001-10, Vol.27 (10), p.1695-1697

2001

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Discovery of TAK-875: A Potent, Selective, and Orally Bioavailable GPR40 Agonist

ACS medicinal chemistry letters, 2010-09, Vol.1 (6), p.290-294

2010

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Discovery of Novel, Highly Potent, and Selective Quinazoline-2-carboxamide-Based Matrix Metalloproteinase (MMP)-13 Inhibitors without a Zinc Binding Group Using a Structure-Based Design Approach

Journal of medicinal chemistry, 2014-11, Vol.57 (21), p.8886-8902

2014

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A comparative study of Video laryngoscope vs Macintosh laryngoscope for prehospital tracheal intubation in Hiroshima, Japan

Resuscitation plus, 2023-03, Vol.13, p.100340-100340, Article 100340

2023

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S11-1 An attempt to teach BASIC BIOLOGY with special attention to human biology

Anthropological Science, 2013-12, Vol.121 (3), p.266-266

2013

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Optimization of (2,3-Dihydro-1-benzofuran-3-yl)acetic Acids: Discovery of a Non-Free Fatty Acid-Like, Highly Bioavailable G Protein-Coupled Receptor 40/Free Fatty Acid Receptor 1 Agonist as a Glucose-Dependent Insulinotropic Agent

Journal of medicinal chemistry, 2012-04, Vol.55 (8), p.3960-3974

2012

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Design, Synthesis, and Biological Activity of Potent and Orally Available G Protein-Coupled Receptor 40 Agonists

Journal of medicinal chemistry, 2011-03, Vol.54 (5), p.1365-1378

2011

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Synthesis and biological evaluation of novel selective androgen receptor modulators (SARMs) Part III: Discovery of 4-(5-oxopyrrolidine-1-yl)benzonitrile derivative 2f as a clinical candidate

Bioorganic & medicinal chemistry, 2017-07, Vol.25 (13), p.3330-3349

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

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

2016

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A Case of Type 2 Diabetes With Infertility Who Safely Conceived and Gave Birth After Bariatric Surgery Due to Preoperative Nutritional Education

Journal of the Japan Diabetes Society, 2021/06/30, Vol.64(6), pp.368-375

2021

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An attempt to teach ‘Basic Biology’ with human biological perspective

Anthropological science. Japanese series, 2014, Vol.122 (1), p.85-88

Santou, Ryobun

2014

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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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Thieno[2,3-d]pyrimidine-2-carboxamides bearing a carboxybenzene group at 5-position: Highly potent, selective, and orally available MMP-13 inhibitors interacting with the S1″ binding site

Bioorganic & medicinal chemistry, 2014-10, Vol.22 (19), p.5487-5505

2014

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Acute subdural haematoma accompanied by anorexia nervosa

BMJ case reports, 2019-09, Vol.12 (9), p.e231156

2019

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Identification of Fused-Ring Alkanoic Acids with Improved Pharmacokinetic Profiles that Act as G Protein-Coupled Receptor 40/Free Fatty Acid Receptor 1 Agonists

Journal of medicinal chemistry, 2012-02, Vol.55 (4), p.1538-1552

2012

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Retraction

Science (American Association for the Advancement of Science), 2022-12, Vol.378 (6626), p.1284-1285

2022

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Retraction

Science (American Association for the Advancement of Science), 2022-12, Vol.378 (6626), p.1285

2022

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RETRACTED: Gradual emergence followed by exponential spread of the SARS-CoV-2 Omicron variant in Africa

Science (American Association for the Advancement of Science), 2022-12, Vol.378 (6623), p.eadd8737-eadd8737

2022

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Synthesis and biological evaluation of novel selective androgen receptor modulators (SARMs). Part II: Optimization of 4-(pyrrolidin-1-yl)benzonitrile derivatives

Bioorganic & medicinal chemistry letters, 2017-05, Vol.27 (9), p.1897-1901

2017

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Discovery of Phenylpropanoic Acid Derivatives Containing Polar Functionalities as Potent and Orally Bioavailable G Protein-Coupled Receptor 40 Agonists for the Treatment of Type 2 Diabetes

Journal of medicinal chemistry, 2012-04, Vol.55 (8), p.3756-3776

2012

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Design, synthesis, and biological evaluation of 4-phenylpyrrole derivatives as novel androgen receptor antagonists

Bioorganic & medicinal chemistry, 2012-01, Vol.20 (1), p.422-434

2012

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Efficacy and safety of linezolid in immunocompromised children with cancer

Pediatrics international, 2010-10, Vol.52 (5), p.694-698

2010

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Retraction

Science (American Association for the Advancement of Science), 2022-12, Vol.378 (6626), p.1284

2022

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TADF activation by solvent freezing: The role of nonradiative triplet decay and spin-orbit coupling in carbazole benzonitrile derivatives

Characteristics and gene cloning of phospholipase D of the psychrophile, Shewanella sp

Secondary closure of neodymium:YAG laser posterior capsulotomy

Discovery of TAK-875: A Potent, Selective, and Orally Bioavailable GPR40 Agonist

Discovery of Novel, Highly Potent, and Selective Quinazoline-2-carboxamide-Based Matrix Metalloproteinase (MMP)-13 Inhibitors without a Zinc Binding Group Using a Structure-Based Design Approach

A comparative study of Video laryngoscope vs Macintosh laryngoscope for prehospital tracheal intubation in Hiroshima, Japan

S11-1 An attempt to teach BASIC BIOLOGY with special attention to human biology

Optimization of (2,3-Dihydro-1-benzofuran-3-yl)acetic Acids: Discovery of a Non-Free Fatty Acid-Like, Highly Bioavailable G Protein-Coupled Receptor 40/Free Fatty Acid Receptor 1 Agonist as a Glucose-Dependent Insulinotropic Agent

Design, Synthesis, and Biological Activity of Potent and Orally Available G Protein-Coupled Receptor 40 Agonists

Synthesis and biological evaluation of novel selective androgen receptor modulators (SARMs) Part III: Discovery of 4-(5-oxopyrrolidine-1-yl)benzonitrile derivative 2f as a clinical candidate

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

A Case of Type 2 Diabetes With Infertility Who Safely Conceived and Gave Birth After Bariatric Surgery Due to Preoperative Nutritional Education

An attempt to teach ‘Basic Biology’ with human biological perspective

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

Thieno[2,3-d]pyrimidine-2-carboxamides bearing a carboxybenzene group at 5-position: Highly potent, selective, and orally available MMP-13 inhibitors interacting with the S1″ binding site

Acute subdural haematoma accompanied by anorexia nervosa

Identification of Fused-Ring Alkanoic Acids with Improved Pharmacokinetic Profiles that Act as G Protein-Coupled Receptor 40/Free Fatty Acid Receptor 1 Agonists

Retraction

Retraction

RETRACTED: Gradual emergence followed by exponential spread of the SARS-CoV-2 Omicron variant in Africa

Synthesis and biological evaluation of novel selective androgen receptor modulators (SARMs). Part II: Optimization of 4-(pyrrolidin-1-yl)benzonitrile derivatives

Discovery of Phenylpropanoic Acid Derivatives Containing Polar Functionalities as Potent and Orally Bioavailable G Protein-Coupled Receptor 40 Agonists for the Treatment of Type 2 Diabetes

Design, synthesis, and biological evaluation of 4-phenylpyrrole derivatives as novel androgen receptor antagonists

Efficacy and safety of linezolid in immunocompromised children with cancer

Retraction

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