15 articles for T Yamada
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Coumarin and chromen-4-one analogues as tautomerase inhibitors of macrophage migration inhibitory factor: discovery and X-ray crystallography.
Yamanouchi Pharmaceutical
Design, synthesis, and properties of des-D-ring interphenylene derivatives of 1α,25-Dihydroxyvitamin D
Kanagawa University
Highly Potent and Oral Macrocyclic Peptides as a HIV-1 Protease Inhibitor: mRNA Display-Derived Hit-to-Lead Optimization.
Shionogi
Structure-activity relationship of N-[2-(dimethylamino)-6-[3-(5-methyl-4-phenyl-1H-imidazol-1-yl)propoxy] phenyl]-N'-pentylurea and analogues. Novel potent inhibitors of acyl-CoA:cholesterol O-acyltransferase with antiatherosclerotic activity.
Eisai
Topographical modification of melanotropin peptide analogues with beta-methyltryptophan isomers at position 9 leads to differential potencies and prolonged biological activities.
University of Arizona
Novel 3alpha-methoxyserrat-14-en-21beta-ol (PJ-1) and 3beta-methoxyserrat-14-en-21beta-ol (PJ-2)-curcumin, kojic acid, quercetin, and baicalein conjugates as HIV agents.
Osaka University of Pharmaceutical Sciences
Methods to determine KDM1A target engagement and chemoprobes useful therefor
Oryzon Genomics
Pyrazole substituted imidazopyrazines as casein kinase 1 d/e inhibitors
Bristol-Myers Squibb
Adenosine receptor agonists, partial agonists, and antagonists
The United States of America, As Represented By The Secretary, Department of Health and Human Services
Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38.
The Scripps Research Institute
2-styrylchromones as novel inhibitors of xanthine oxidase. A structure-activity study.
University of Porto-Rua Anibal Cunha