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Neuromuscular stimulation ameliorates ischemia-induced walking impairment in the rat claudication model

The journal of physiological sciences, 2019-11, Vol.69 (6), p.885-893

2019

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Discovery and pharmacological effects of a novel GPR142 antagonist

Journal of receptors and signal transduction, 2017-05, Vol.37 (3), p.290-296

2017

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Novel Oral Derivative UD-017, a Highly Selective CDK7 Inhibitor, Exhibits Anticancer Activity by Inducing Cell-Cycle Arrest and Apoptosis in Human Colorectal Cancer

Hiroshima Journal of Medical Sciences, 2020/03/31, Vol.69(1), pp.23-31

2020

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Discovery and optimization of a novel series of GPR142 agonists for the treatment of type 2 diabetes mellitus

Bioorganic & medicinal chemistry letters, 2012-09, Vol.22 (18), p.5942-5947

2012

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Novel Keap1-Nrf2 Protein-Protein Interaction Inhibitor UBE-1099 Ameliorates Progressive Phenotype in Alport Syndrome Mouse Model

Kidney360, 2022-04, Vol.3 (4), p.687-699

2022

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Identification of metals from osteoblastic ST-2 cell supernatants as novel OGR1 agonists

Journal of receptors and signal transduction, 2015-09, Vol.35 (5), p.485-492

2015

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MRGD, a MAS-related G-protein coupled receptor, promotes tumorigenisis and is highly expressed in lung cancer

PloS one, 2012-06, Vol.7 (6), p.e38618

2012

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Purification and Identification of Activating Enzymes of CS-0777, a Selective Sphingosine 1-Phosphate Receptor 1 Modulator, in Erythrocytes

The Journal of biological chemistry, 2011-07, Vol.286 (28), p.24765-24775

2011

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Novel CC chemokine receptor 4 antagonist RS-1154 inhibits ovalbumin-induced ear swelling in mice

European journal of pharmacology, 2009-12, Vol.624 (1), p.38-44

2009

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Identification of physiologically active substances as novel ligands for MRGPRD

BioMed research international, 2012-01, Vol.2012, p.816159-9

2012

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RS-1748, a Novel CC Chemokine Receptor 4 Antagonist, Inhibits Ovalbumin-Induced Airway Inflammation in Guinea Pigs

Biological and Pharmaceutical Bulletin, 2010/06/01, Vol.33(6), pp.1067-1069

2010

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Discovery of CS-2100, a potent, orally active and S1P3-sparing S1P1 agonist

Bioorganic & medicinal chemistry letters, 2012-02, Vol.22 (4), p.1788-1792

2012

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Potent and Orally Bioavailable GPR142 Agonists as Novel Insulin Secretagogues for the Treatment of Type 2 Diabetes

ACS medicinal chemistry letters, 2013-08, Vol.4 (8), p.790-794

2013

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MO578: UBE-1099, A Novel Non-Covalent Keap1-NRF2 Inhibitor, Protects Against Renal Ischemia-Reperfusion Injury

Nephrology, dialysis, transplantation, 2022-05, Vol.37 (Supplement_3)

2022

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UBE-1099, a Novel Non-Covalent Keap1-Nrf2 Inhibitor, Protects Against Renal Ischemia-Reperfusion Injury via Nrf2 Activation: PO2508

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.762-762

2021

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Nerve Growth Factor-induced Glutamate Release Is via p75 Receptor, Ceramide, and Ca2+ from Ryanodine Receptor in Developing Cerebellar Neurons

The Journal of biological chemistry, 2003-10, Vol.278 (42), p.41259-41269

2003

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Ascotricins A and B, novel antagonists of sphingosine-1-phosphate receptor 1 from Ascotricha chartarum Berk. SANK 14186

Journal of antibiotics, 2009-07, Vol.62 (7), p.359-364

2009

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A Novel Sphingosine-1-Phosphate Receptor 1 Antagonist Prevents the Proliferation and Relaxation of Vascular Endothelial Cells by Sphingosine-1-Phosphate

Biological and Pharmaceutical Bulletin, 2010/09/01, Vol.33(9), pp.1500-1505

2010

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Identification of sulfonylpyrimidines as novel selective aldosterone synthase (CYP11B2) inhibitors

Bioorganic & medicinal chemistry, 2024-06, Vol.108, p.117775, Article 117775

2024

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Synthesis and SAR of 1,3-thiazolyl thiophene and pyridine derivatives as potent, orally active and S1P3-sparing S1P1 agonists

Bioorganic & medicinal chemistry letters, 2012-05, Vol.22 (9), p.3083-3088

2012

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Synthesis and evaluation of CS-2100, a potent, orally active and S1P3- sparing S1P1 agonist

European journal of medicinal chemistry, 2012-05, Vol.51, p.92-98

2012

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Novel Keap-Nrf2 Protein-Protein Interaction Inhibitor UBE-1099 Ameliorates the Severity of Experimental Alport Syndrome: PO1302

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.418-418

2021

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Dichloroacetate induces regulatory T‐cell differentiation and suppresses Th17‐cell differentiation by pyruvate dehydrogenase kinase‐independent mechanism

Journal of pharmacy and pharmacology, 2017-01, Vol.69 (1), p.43-51

2017

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Deorphanization of Dresden G Protein-Coupled Receptor for an Odorant Receptor

Journal of receptors and signal transduction, 2007-01, Vol.27 (4), p.323-334

2007

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Synthesis and SAR studies of a novel class of S1P1 receptor antagonists

Bioorganic & medicinal chemistry, 2007-05, Vol.15 (10), p.3548-3564

2007

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Neuromuscular stimulation ameliorates ischemia-induced walking impairment in the rat claudication model

Discovery and pharmacological effects of a novel GPR142 antagonist

Novel Oral Derivative UD-017, a Highly Selective CDK7 Inhibitor, Exhibits Anticancer Activity by Inducing Cell-Cycle Arrest and Apoptosis in Human Colorectal Cancer

Discovery and optimization of a novel series of GPR142 agonists for the treatment of type 2 diabetes mellitus

Novel Keap1-Nrf2 Protein-Protein Interaction Inhibitor UBE-1099 Ameliorates Progressive Phenotype in Alport Syndrome Mouse Model

Identification of metals from osteoblastic ST-2 cell supernatants as novel OGR1 agonists

MRGD, a MAS-related G-protein coupled receptor, promotes tumorigenisis and is highly expressed in lung cancer

Purification and Identification of Activating Enzymes of CS-0777, a Selective Sphingosine 1-Phosphate Receptor 1 Modulator, in Erythrocytes

Novel CC chemokine receptor 4 antagonist RS-1154 inhibits ovalbumin-induced ear swelling in mice

Identification of physiologically active substances as novel ligands for MRGPRD

RS-1748, a Novel CC Chemokine Receptor 4 Antagonist, Inhibits Ovalbumin-Induced Airway Inflammation in Guinea Pigs

Discovery of CS-2100, a potent, orally active and S1P3-sparing S1P1 agonist

Potent and Orally Bioavailable GPR142 Agonists as Novel Insulin Secretagogues for the Treatment of Type 2 Diabetes

MO578: UBE-1099, A Novel Non-Covalent Keap1-NRF2 Inhibitor, Protects Against Renal Ischemia-Reperfusion Injury

UBE-1099, a Novel Non-Covalent Keap1-Nrf2 Inhibitor, Protects Against Renal Ischemia-Reperfusion Injury via Nrf2 Activation: PO2508

Nerve Growth Factor-induced Glutamate Release Is via p75 Receptor, Ceramide, and Ca2+ from Ryanodine Receptor in Developing Cerebellar Neurons

Ascotricins A and B, novel antagonists of sphingosine-1-phosphate receptor 1 from Ascotricha chartarum Berk. SANK 14186

A Novel Sphingosine-1-Phosphate Receptor 1 Antagonist Prevents the Proliferation and Relaxation of Vascular Endothelial Cells by Sphingosine-1-Phosphate

Identification of sulfonylpyrimidines as novel selective aldosterone synthase (CYP11B2) inhibitors

Synthesis and SAR of 1,3-thiazolyl thiophene and pyridine derivatives as potent, orally active and S1P3-sparing S1P1 agonists

Synthesis and evaluation of CS-2100, a potent, orally active and S1P3- sparing S1P1 agonist

Novel Keap-Nrf2 Protein-Protein Interaction Inhibitor UBE-1099 Ameliorates the Severity of Experimental Alport Syndrome: PO1302

Dichloroacetate induces regulatory T‐cell differentiation and suppresses Th17‐cell differentiation by pyruvate dehydrogenase kinase‐independent mechanism

Deorphanization of Dresden G Protein-Coupled Receptor for an Odorant Receptor

Synthesis and SAR studies of a novel class of S1P1 receptor antagonists

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