Madoka Kawamura
Saitama, 3319530, Japan
Last Updated: 09/26/2026
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Found 9 publications
Introduction of a carboxylic acid group into pyrazolylpyridine derivatives increased selectivity for inhibition of the 20-HETE synthase CYP4A11/4F2.
Journal: Bioorganic & medicinal chemistry
Published: September 01, 2023
Discovery of Novel Pyrazolylpyridine Derivatives for 20-Hydroxyeicosatetraenoic Acid Synthase Inhibitors with Selective CYP4A11/4F2 Inhibition.
Journal: Journal of medicinal chemistry
Published: November 01, 2022
Synthesis and Structure-Activity Relationship of C-Phenyl D-Glucitol (TP0454614) Derivatives as Selective Sodium-Dependent Glucose Cotransporter 1 (SGLT1) Inhibitors.
Journal: Chemical & pharmaceutical bulletin
Published: July 03, 2020
Design, synthesis and biological evaluation of novel 7-azaspiro[3.5]nonane derivatives as GPR119 agonists.
Journal: Bioorganic & medicinal chemistry
Published: November 09, 2017
Novel 3H-[1,2,3]triazolo[4,5-c]pyridine derivatives as GPR119 agonists: Synthesis and structure-activity/solubility relationships.
Journal: Bioorganic & medicinal chemistry
Published: March 21, 2017
Design and synthesis of 1H-pyrazolo[3,4-c]pyridine derivatives as a novel structural class of potent GPR119 agonists.
Journal: Bioorganic & medicinal chemistry letters
Published: March 29, 2016
Isoquinoline derivatives as potent, selective, and orally active CRTH2 antagonists.
Journal: Chemical & pharmaceutical bulletin
Published: June 03, 2014
Isoquinoline derivatives as potent CRTH2 antagonists: design, synthesis and SAR.
Journal: Bioorganic & medicinal chemistry
Published: September 05, 2013
Isoquinoline derivatives as potent CRTH2 receptor antagonists: synthesis and SAR.
Journal: Bioorganic & medicinal chemistry letters
Published: December 29, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026