SUNAZUKA Toshiaki | Research Center for Biological Function, The Kitasato Institute and School of Pharmaceutical Science

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著作論文

New Analogs of the Pyripyropene Family of ACAT Inhibitors via α-Pyrone Fragmentation and γ-Acylation/Cyclization
Efficient Chemical Conversion of Louisianin A to C and D, The Inhibitor of Angiogenesis
Synthesis and Anti-platelet Aggregation Activity of Water-soluble Staurosporine Derivatives
Effect of 14-Membered Ring Macrolide Compounds on Rat Leucocyte Chemotaxis and the Structure-activity Relationships
Effcects of Erythromycin and Its Derivatives on Interlcukin-8 Release by Human Bronchial Epithelial Cell Line BEAS-2B Cells
Synthesis and Antiangiogenic Activity of Staurosporine Derivatives
Chemical Modification and Structure-activity Relationships of Pyripyropenes 1. Modification at the Four Hydroxyl Groups
Structure-activity Relationships of Pyripyropenes Fungal Acyl-CoA:Cholesterol Acyltransferase Inhibitors
Determination of Absolute Stereochemistries of Arisugacin F and Territrem B, Novel Acetylcholinesterase Inhibitors
Convergent Synthesis of Arisugacin Skeletons and Their Acetylcholinesterase Inhibitory Activity
Structure-activity Relationships Study of Pyripyropenes : Reversal of Cancer Cell Multidrug Resistance
Structure-activity Relationships of Lactacystin, the First Non-protein Neurotrophic Factor
Arisugacins C and D, Novel Acetyicholinesterase Inhibitors and Their Related Novel Metabolites Produced by Penicillium sp. FO-4259-11
Chemical Modification and Structure-activity Relationships of Pyripyropenes 2. 1,11-Cyclic Analogs
Syntheses and Absolute Structures of Novel Protein Farnesyltransferase Inhibitors, Kurasoins A and B
Chemical Modification and Structure-activity Relationships of Pyripyropenes 3. Synthetic Conversion of Pyridine-pyrone Moiety
Arisugacin, a Novel and Selective Inhibitor of Acetylcholinesterase from Penicillium sp.FO-4259

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