Satoshi Sogabe
Fujisawa, 2518555, Japan
Last Updated: 09/26/2026
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Found 25 publications
Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl Moiety.
Journal: Journal of medicinal chemistry
Published: July 30, 2021
Author Correction: Strictly regulated agonist-dependent activation of AMPA-R is the key characteristic of TAK-653 for robust synaptic responses and cognitive improvement.
Journal: Scientific reports
Published: July 22, 2021
Identification of the first highly selective inhibitor of human lactate dehydrogenase B.
Journal: Scientific reports
Published: July 16, 2021
Strictly regulated agonist-dependent activation of AMPA-R is the key characteristic of TAK-653 for robust synaptic responses and cognitive improvement.
Journal: Scientific reports
Published: April 23, 2021
Design, Synthesis, and Evaluation of Piperazinyl Pyrrolidin-2-ones as a Novel Series of Reversible Monoacylglycerol Lipase Inhibitors.
Journal: Journal of medicinal chemistry
Published: September 26, 2018
TAK-137, an AMPA-R potentiator with little agonistic effect, has a wide therapeutic window.
Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
Published: April 02, 2018
Discovery of an Irreversible and Cell-Active BCL6 Inhibitor Selectively Targeting Cys53 Located at the Protein-Protein Interaction Interface.
Journal: Biochemistry
Published: January 03, 2018
HBT1, a Novel AMPA Receptor Potentiator with Lower Agonistic Effect, Avoided Bell-Shaped Response in In Vitro BDNF Production.
Journal: The Journal of pharmacology and experimental therapeutics
Published: September 11, 2017
Discovery of a novel B-cell lymphoma 6 (BCL6)-corepressor interaction inhibitor by utilizing structure-based drug design.
Journal: Bioorganic & medicinal chemistry
Published: June 10, 2017
Discovery of a B-Cell Lymphoma 6 Protein-Protein Interaction Inhibitor by a Biophysics-Driven Fragment-Based Approach.
Journal: Journal of medicinal chemistry
Published: May 05, 2017
Crystal Structure of a Human K-Ras G12D Mutant in Complex with GDP and the Cyclic Inhibitory Peptide KRpep-2d.
Journal: ACS medicinal chemistry letters
Published: March 23, 2017
Discovery of a Kelch-like ECH-associated protein 1-inhibitory tetrapeptide and its structural characterization.
Journal: Biochemical and biophysical research communications
Published: March 10, 2017
Last Updated: 09/26/2026