Masakazu Atobe
Izunokuni, 4102321, Japan
Last Updated: 09/26/2026
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Found 16 publications
α-Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping.
Journal: Angewandte Chemie (International ed. in English)
Published: September 26, 2023
Exploration of piperidine 3D fragment chemical space: synthesis and 3D shape analysis of fragments derived from 20 regio- and diastereoisomers of methyl substituted pipecolinates.
Journal: RSC medicinal chemistry
Published: July 22, 2022
Discovery of 4,6- and 5,7-Disubstituted Isoquinoline Derivatives as a Novel Class of Protein Kinase C ζ Inhibitors with Fragment-Merging Strategy.
Journal: Journal of medicinal chemistry
Published: June 20, 2020
Design and Synthesis of 56 Shape-Diverse 3D Fragments.
Journal: Chemistry (Weinheim an der Bergstrasse, Germany)
Published: March 04, 2020
Activation of Transient Receptor Potential Vanilloid (TRPV) 4 as a Therapeutic Strategy in Osteoarthritis.
Journal: Current topics in medicinal chemistry
Published: June 18, 2019
Discovery of Novel Transient Receptor Potential Vanilloid 4 (TRPV4) Agonists as Regulators of Chondrogenic Differentiation: Identification of Quinazolin-4(3 H)-ones and in Vivo Studies on a Surgically Induced Rat Model of Osteoarthritis.
Journal: Journal of medicinal chemistry
Published: January 11, 2019
Discovery of a novel 2-(1H-pyrazolo[3,4-b]pyridin-1-yl)thiazole derivative as an EP1 receptor antagonist and in vivo studies in a bone fracture model.
Journal: Bioorganic & medicinal chemistry letters
Published: April 13, 2018
A series of novel indazole derivatives of Sirt 1 activator as osteogenic regulators.
Journal: Bioorganic & medicinal chemistry letters
Published: August 09, 2017
Increase of enzyme activity through specific covalent modification with fragments.
Journal: Chemical science
Published: May 02, 2017
Lead-oriented synthesis: Investigation of organolithium-mediated routes to 3-D scaffolds and 3-D shape analysis of a virtual lead-like library.
Journal: Bioorganic & medicinal chemistry
Published: February 09, 2015
Discovery of 2-(1H-indazol-1-yl)-thiazole derivatives as selective EP(1) receptor antagonists for treatment of overactive bladder by core structure replacement.
Journal: Bioorganic & medicinal chemistry letters
Published: November 05, 2013
SAR-based optimization of 2-(1H-pyrazol-1-yl)-thiazole derivatives as highly potent EP1 receptor antagonists.
Journal: Bioorganic & medicinal chemistry letters
Published: September 14, 2013
Last Updated: 09/26/2026