15 articles for M Otsuka
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Inhibitory activities against topoisomerase I and II by isoaurostatin derivatives and their structure-activity relationships.

Kumamoto University
Synthesis and biological evaluation of derivatives of 2-{2-fluoro-4-[(2-oxocyclopentyl)methyl]phenyl}propanoic acid: nonsteroidal anti-inflammatory drugs with low gastric ulcerogenic activity.

Keio University
Design and synthesis of biotinylated inositol 1,3,4,5-tetrakisphosphate targeting Grp1 pleckstrin homology domain.

Kumamoto Health Science University
Synthesis and biological evaluation of loxoprofen derivatives.

Kumamoto University
Identification of a New Series of STAT3 Inhibitors by Virtual Screening.

TBA
Properties and synthesis of 2-{2-fluoro (or bromo)-4-[(2-oxocyclopentyl)methyl]phenyl}propanoic acid: nonsteroidal anti-inflammatory drugs with low membrane permeabilizing and gastric lesion-producing activities.

Kumamoto University
Ligand-based design and synthesis of new trityl histamine and trityl cysteamine derivatives as SIRT2 inhibitors for cancer therapy.

South Valley University
Selective SIRT2 inhibitors as promising anticancer therapeutics: An update from 2016 to 2020.

Minia University
Crystal Structures of Metallo-β-Lactamase (IMP-1) and Its D120E Mutant in Complexes with Citrate and the Inhibitory Effect of the Benzyl Group in Citrate Monobenzyl Ester.

Kumamoto University
Fluorophenylalkyl-substituted cyanoguanidine derivatives as bacteria-selective MATE transporter inhibitors for the treatment of antibiotic-resistant infections.

Setsunan University
Inhibitory activities against topoisomerase I and II by polyhydroxybenzoyl amide derivatives and their structure-activity relationship.

Kumamoto University
A novel metal-chelating inhibitor of protein farnesyltransferase.

Kumamoto University
Structure activity study of S-trityl-cysteamine dimethylaminopyridine derivatives as SIRT2 inhibitors: Improvement of SIRT2 binding and inhibition.

Science Farm
Design, synthesis and biological evaluation of a new series of thiazolyl-pyrazolines as dual EGFR and HER2 inhibitors.

Anadolu University
New SIRT2 inhibitors: Histidine-based bleomycin spin-off.

Kumamoto University