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15 articles for M Otsuka


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Inhibitory activities against topoisomerase I and II by isoaurostatin derivatives and their structure-activity relationships.EBI
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.EBI
Keio University
Design and synthesis of biotinylated inositol 1,3,4,5-tetrakisphosphate targeting Grp1 pleckstrin homology domain.EBI
Kumamoto Health Science University
Synthesis and biological evaluation of loxoprofen derivatives.EBI
Kumamoto University
Identification of a New Series of STAT3 Inhibitors by Virtual Screening.EBI
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.EBI
Kumamoto University
Ligand-based design and synthesis of new trityl histamine and trityl cysteamine derivatives as SIRT2 inhibitors for cancer therapy.EBI
South Valley University
Selective SIRT2 inhibitors as promising anticancer therapeutics: An update from 2016 to 2020.EBI
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.EBI
Kumamoto University
Fluorophenylalkyl-substituted cyanoguanidine derivatives as bacteria-selective MATE transporter inhibitors for the treatment of antibiotic-resistant infections.EBI
Setsunan University
Inhibitory activities against topoisomerase I and II by polyhydroxybenzoyl amide derivatives and their structure-activity relationship.EBI
Kumamoto University
A novel metal-chelating inhibitor of protein farnesyltransferase.EBI
Kumamoto University
Structure activity study of S-trityl-cysteamine dimethylaminopyridine derivatives as SIRT2 inhibitors: Improvement of SIRT2 binding and inhibition.EBI
Science Farm
Design, synthesis and biological evaluation of a new series of thiazolyl-pyrazolines as dual EGFR and HER2 inhibitors.EBI
Anadolu University
New SIRT2 inhibitors: Histidine-based bleomycin spin-off.EBI
Kumamoto University