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Suspected cholestatic liver injury induced by favipiravir in a patient with COVID-19

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2021-02, Vol.27 (2), p.390-392

2021

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Exploration of LPS2 agonist binding modes using the combination of a new hydrophobic scaffold and homology modeling

European journal of medicinal chemistry, 2023-04, Vol.252, p.115271-115271, Article 115271

2023

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Switching Lysophosphatidylserine G Protein-Coupled Receptor Agonists to Antagonists by Acylation of the Hydrophilic Serine Amine

Journal of medicinal chemistry, 2021-07, Vol.64 (14), p.10059-10101

2021

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Non-naturally Occurring Helical Molecules Can Interfere with p53–MDM2 and p53–MDMX Protein–Protein Interactions

Chemical and Pharmaceutical Bulletin, 2019/10/01, Vol.67(10), pp.1139-1143

2019

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Non-naturally Occurring Regio Isomer of Lysophosphatidylserine Exhibits Potent Agonistic Activity toward G Protein-Coupled Receptors

Journal of medicinal chemistry, 2020-09, Vol.63 (17), p.9990-10029

2020

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Isosteric Replacement of Ester Linkage of Lysophospholipids with Heteroaromatic Rings Retains Potency and Subtype Selectivity

Chemical and Pharmaceutical Bulletin, 2023/07/01, Vol.71(7), pp.584-615

2023

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Structure–Activity Relationships of Lysophosphatidylserine Analogs as Agonists of G‑Protein-Coupled Receptors GPR34, P2Y10, and GPR174

Journal of medicinal chemistry, 2015-05, Vol.58 (10), p.4204-4219

2015

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Probing the Hydrophobic Binding Pocket of G‑Protein-Coupled Lysophosphatidylserine Receptor GPR34/LPS1 by Docking-Aided Structure–Activity Analysis

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.6384-6399

2017

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Non-naturally Occurring Helical Molecules Can Interfere with p53-MDM2 and p53-MDMX Protein-Protein Interactions

Chemical and Pharmaceutical Bulletin, 2019-10, Vol.67 (10), p.1139-1143

2019

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Lysophosphatidylserine analogues differentially activate three LysoPS receptors

Journal of biochemistry (Tokyo), 2015-03, Vol.157 (3), p.151-160

2015

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Leucine 434 is essential for docosahexaenoic acid–induced augmentation of L-glutamate transporter current

The Journal of biological chemistry, 2023-01, Vol.299 (1), p.102793-102793, Article 102793

2023

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Correction: Leucine 434 is essential for docosahexaenoic acid–induced augmentation of L-glutamate transporter current

The Journal of biological chemistry, 2023-07, Vol.299 (7), p.104931-104931, Article 104931

2023

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Not That DDT: A Databank of Dynamics Trajectories for Organic Reactions

Journal of chemical education, 2022-07, Vol.99 (7), p.2721-2725

2022

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Membrane Phospholipid Analogues as Molecular Rulers to Probe the Position of the Hydrophobic Contact Point of Lysophospholipid Ligands on the Surface of G‑Protein-Coupled Receptor during Membrane Approach

Biochemistry (Easton), 2020-03, Vol.59 (11), p.1173-1201

2020

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Structural insights into ligand recognition by the lysophosphatidic acid receptor LPA 6

Nature (London), 2017-08, Vol.548 (7667), p.356

2017

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Gタンパク質共役型受容体の下流応答がリガンド構造にいかに制御されるか

ファルマシア, 2021, Vol.57(9), pp.855-855

佐山, 美紗

2021

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Conformational Constraint of the Glycerol Moiety of Lysophosphatidylserine Affords Compounds with Receptor Subtype Selectivity

Journal of medicinal chemistry, 2016-04, Vol.59 (8), p.3750-3776

2016

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Exploration of LPS 2 agonist binding modes using the combination of a new hydrophobic scaffold and homology modeling

European journal of medicinal chemistry, 2023-04, Vol.252, p.115271

2023

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Probing the Hydrophobic Binding Pocket of G-Protein-Coupled Lysophosphatidylserine Receptor GPR34/LPS 1 by Docking-Aided Structure-Activity Analysis

Journal of medicinal chemistry, 2017-07, Vol.60 (14), p.6384-6399

2017

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Structural insights into ligand recognition by the lysophosphatidic acid receptor LPA6

Nature (London), 2017-08, Vol.548 (7667), p.356-360

2017

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Identification of lysophosphatidylthreonine with an aromatic fatty acid surrogate as a potent inducer of mast cell degranulation

Biochemistry and biophysics reports, 2016-12, Vol.8, p.346-351

2016

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Cyclooxygenase-2/Prostaglandin D2/CRTH2 Pathway Mediates Double-Stranded RNA-Induced Enhancement of Allergic Airway Inflammation

The Journal of immunology (1950), 2008-01, Vol.180 (1), p.541-549

2008

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Prostaglandin D2-induced eosinophilic airway inflammation is mediated by CRTH2 receptor

The Journal of pharmacology and experimental therapeutics, 2005-03, Vol.312 (3), p.954

2005

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Prostaglandin D 2 -Induced Eosinophilic Airway Inflammation Is Mediated by CRTH2 Receptor

The Journal of pharmacology and experimental therapeutics, 2005-03, Vol.312 (3), p.954-960

2005

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Strain-Specific Phenotypes of Airway Inflammation and Bronchial Hyperresponsiveness Induced by Epicutaneous Allergen Sensitization in BALB/c and C57BL/6 Mice

International archives of allergy and immunology, 2010-01, Vol.152 (Suppl 1), p.67-74

2010

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Suspected cholestatic liver injury induced by favipiravir in a patient with COVID-19

Exploration of LPS2 agonist binding modes using the combination of a new hydrophobic scaffold and homology modeling

Switching Lysophosphatidylserine G Protein-Coupled Receptor Agonists to Antagonists by Acylation of the Hydrophilic Serine Amine

Non-naturally Occurring Helical Molecules Can Interfere with p53–MDM2 and p53–MDMX Protein–Protein Interactions

Non-naturally Occurring Regio Isomer of Lysophosphatidylserine Exhibits Potent Agonistic Activity toward G Protein-Coupled Receptors

Isosteric Replacement of Ester Linkage of Lysophospholipids with Heteroaromatic Rings Retains Potency and Subtype Selectivity

Structure–Activity Relationships of Lysophosphatidylserine Analogs as Agonists of G‑Protein-Coupled Receptors GPR34, P2Y10, and GPR174

Probing the Hydrophobic Binding Pocket of G‑Protein-Coupled Lysophosphatidylserine Receptor GPR34/LPS1 by Docking-Aided Structure–Activity Analysis

Non-naturally Occurring Helical Molecules Can Interfere with p53-MDM2 and p53-MDMX Protein-Protein Interactions

Lysophosphatidylserine analogues differentially activate three LysoPS receptors

Leucine 434 is essential for docosahexaenoic acid–induced augmentation of L-glutamate transporter current

Correction: Leucine 434 is essential for docosahexaenoic acid–induced augmentation of L-glutamate transporter current

Not That DDT: A Databank of Dynamics Trajectories for Organic Reactions

Membrane Phospholipid Analogues as Molecular Rulers to Probe the Position of the Hydrophobic Contact Point of Lysophospholipid Ligands on the Surface of G‑Protein-Coupled Receptor during Membrane Approach

Structural insights into ligand recognition by the lysophosphatidic acid receptor LPA 6

Gタンパク質共役型受容体の下流応答がリガンド構造にいかに制御されるか

Conformational Constraint of the Glycerol Moiety of Lysophosphatidylserine Affords Compounds with Receptor Subtype Selectivity

Exploration of LPS 2 agonist binding modes using the combination of a new hydrophobic scaffold and homology modeling

Probing the Hydrophobic Binding Pocket of G-Protein-Coupled Lysophosphatidylserine Receptor GPR34/LPS 1 by Docking-Aided Structure-Activity Analysis

Structural insights into ligand recognition by the lysophosphatidic acid receptor LPA6

Identification of lysophosphatidylthreonine with an aromatic fatty acid surrogate as a potent inducer of mast cell degranulation

Cyclooxygenase-2/Prostaglandin D2/CRTH2 Pathway Mediates Double-Stranded RNA-Induced Enhancement of Allergic Airway Inflammation

Prostaglandin D2-induced eosinophilic airway inflammation is mediated by CRTH2 receptor

Prostaglandin D 2 -Induced Eosinophilic Airway Inflammation Is Mediated by CRTH2 Receptor

Strain-Specific Phenotypes of Airway Inflammation and Bronchial Hyperresponsiveness Induced by Epicutaneous Allergen Sensitization in BALB/c and C57BL/6 Mice

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