Satohsi Shuto
0000-0001-7850-8064
7 papers found
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A macrocyclic peptide library with a structurally constrained cyclopropane‐containing building block leads to thiol‐independent inhibitors of phosphoglycerate mutase
Development of a Highly Potent Analogue and a Long-Acting Analogue of Oxytocin for the Treatment of Social Impairment-Like Behaviors
Frontispiece: From Peptides to Peptidomimetics: A Strategy Based on the Structural Features of Cyclopropane
From Peptides to Peptidomimetics: A Strategy Based on the Structural Features of Cyclopropane
Cyclopropane-Based Peptidomimetics Mimicking Wide-Ranging Secondary Structures of Peptides: Conformational Analysis and Their Use in Rational Ligand Optimization
Cover Picture: Highly Conformationally Restricted Cyclopropane Tethers with Three-Dimensional Structural Diversity Drastically Enhance the Cell Permeability of Cyclic Peptides (Chem. Eur. J. 13/2017)
Highly Conformationally Restricted Cyclopropane Tethers with Three-Dimensional Structural Diversity Drastically Enhance the Cell Permeability of Cyclic Peptides
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