Teruki Hamada

Fujisawa, Japan

Last Updated: 09/26/2026

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Found 13 publications

Xenogenic Engraftment of Human-Induced Pluripotent Stem Cell-Derived Pancreatic Islet Cells in an Immunosuppressive Diabetic Göttingen Mini-Pig Model.

Xenogenic Engraftment of Human-Induced Pluripotent Stem Cell-Derived Pancreatic Islet Cells in an Immunosuppressive Diabetic Göttingen Mini-Pig Model.

Journal: Cell transplantation

Published: October 14, 2024

Design and Identification of a GPR40 Full Agonist (SCO-267) Possessing a 2-Carbamoylphenyl Piperidine Moiety.

Design and Identification of a GPR40 Full Agonist (SCO-267) Possessing a 2-Carbamoylphenyl Piperidine Moiety.

Journal: Journal of medicinal chemistry

Published: September 09, 2020

Microminipig: A suitable animal model to estimate oral absorption of sustained-release formulation in humans.

Microminipig: A suitable animal model to estimate oral absorption of sustained-release formulation in humans.

Journal: International journal of pharmaceutics

Published: January 07, 2020

Development of novel highly sensitive methods to detect endogenous cGAMP in cells and tissue.

Development of novel highly sensitive methods to detect endogenous cGAMP in cells and tissue.

Journal: Journal of immunological methods

Published: June 03, 2019

Direct Drug Delivery of Low-Permeable Compounds to the Central Nervous System Via Intranasal Administration in Rats and Monkeys.

Direct Drug Delivery of Low-Permeable Compounds to the Central Nervous System Via Intranasal Administration in Rats and Monkeys.

Journal: Pharmaceutical research

Published: November 15, 2018

Design and synthesis of 1-(1-benzothiophen-7-yl)-1H-pyrazole, a novel series of G protein-coupled receptor 52 (GPR52) agonists.

Design and synthesis of 1-(1-benzothiophen-7-yl)-1H-pyrazole, a novel series of G protein-coupled receptor 52 (GPR52) agonists.

Journal: Bioorganic & medicinal chemistry

Published: October 27, 2017

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 imidazo[1,2-b]pyridazine-based p38 MAP kinase inhibitors.

Journal: Bioorganic & medicinal chemistry

Published: September 20, 2017

Mechanism-Based Pharmacokinetic/Pharmacodynamic Modeling of the Glucagon-Like Peptide-1 Receptor Agonist Exenatide to Characterize Its Antiobesity Effects in Diet-Induced Obese Mice.

Mechanism-Based Pharmacokinetic/Pharmacodynamic Modeling of the Glucagon-Like Peptide-1 Receptor Agonist Exenatide to Characterize Its Antiobesity Effects in Diet-Induced Obese Mice.

Journal: The Journal of pharmacology and experimental therapeutics

Published: May 04, 2017

Identification of a novel fluoropyrrole derivative as a potassium-competitive acid blocker with long duration of action.

Identification of a novel fluoropyrrole derivative as a potassium-competitive acid blocker with long duration of action.

Journal: Bioorganic & medicinal chemistry

Published: March 11, 2017

Design, synthesis and biological evaluation of a novel series of peripheral-selective noradrenaline reuptake inhibitor.

Design, synthesis and biological evaluation of a novel series of peripheral-selective noradrenaline reuptake inhibitor.

Journal: Bioorganic & medicinal chemistry

Published: April 12, 2015

Discovery of the first potent and orally available agonist of the orphan G-protein-coupled receptor 52.

Discovery of the first potent and orally available agonist of the orphan G-protein-coupled receptor 52.

Journal: Journal of medicinal chemistry

Published: June 03, 2014

Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonists.

Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonists.

Journal: Bioorganic & medicinal chemistry

Published: May 28, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026