TSUDA Yuko | Faculty of Pharmaceutical Sciences, Kobe Gakuin University

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著作論文

Synthesis of Endomorphin-2Analogues Containing Piperidinecarboxylic Acid (Pip) and 2-Azetidinecarboxylic Acid (Aze)
Synthesis and Biological Activity of Endomorphin-2 Analogues Containing Pro Mimics
Synthesis and Binding Activities of Endomorphin Analogs Containing 1-Aminocyclopropane-1-carboxylic Acid
Amino Acids and Peptides. LV. Application of 2-Adamantyl Dericatives as Protecting Groups to the Synthesis of Peptide Fragments Related to Sulfolobus solifataricus Ribonuclease. II
Amino Acids and Peptides. LIV. Application of 2-Adamantyl Derivatives as Protecting Groups to the Synthesis of Peptide Fragments Related to Sulfolobus solifataricus Ribonuclease. I
Differential Receptor Recognition by Dmt-Containing Enkephalin Dimers Cross-Linked by Phenylenediamines
Deprotection of the Indole (N^)_Formyl (For) Group on Tryptophan Employing a New Reagent, N,N'-Dimethylethylendiamine (DMEDA) in an Aqueous Solution
Development of μ-Receptor Selective Opioid Mimetics Derived from Endomorphin Sequences
SYNTHESIS OF EGLIN C AND DEVELOPMENT OF INHIBITORS AGAINST HUMAN LEUKOCYTE ELASTASE AND CATHEPSIN G
Synthesis of Peptide Chloromethyl Ketones and Examination of Their Inhibitory Effects on Human Spleen Fibrinolytic Proteinase (SFP) and Human Leukocyte Elastase (LE)(Organic,Chemical)
The Antiproliferative Activities of Somatostatin Analogs on Various Tumor Cells
Studies on the Mechanism of 1,2-Dihydropyrazin-2-one Ring Formation from Dipeptidyl Chloromethyl Ketone and Its Chemical Properties : Immediate Deamination during Catalytic Hydrogenation
Synthesis of Somatostatin Analogs and Their Antitumor Activities
The Structure-Activity Relationship of Dmt-NH-X
Synthesis of New Pyrazinone Ring-Containing Opioid Mimetics and Studies on Their Structure-Activity Relationship
Synthesis of Opioid Mimetics Containing a Pyrazinone Ring and Their Activities
Structure-Inhibitory Activity Relationship of Plasmin and Plasma Kallikrein Inhibitors^
Isolation of Plasma Kallikrein by High Efficiency Affinity Chromatography and Its Characterization
Structure-Inhibitory Activity Relationships of Plasmin and Plasma Kallikrein Inhibitors
Binding Diversity of a Noncovalent-Type Low-Molecular-Weight Serine Protease Inhibitor and Function of a Catalytic Water Molecule : X-Ray Crystal Structure of PKSI-527-Inhibited Trypsin
Synthesis of Pyrazinone Ring-Containing Opioid Mimetics and Examination of Their Opioid Receptor-Binding Activity
Design and Synthesis of Pyrazinone Ring-Containing Opioid Mimetics and Examination of Their Opioid Receptor-Binding Activity
Synthesis of Endomorphin Analogs and Studies on the Structure-Opioid Receptor-Binding Activity Relationship
Studies on the Stable Structure and Inhibitory Activity of Plasmin and Plasma Kallikrein Inhibitors Using the MM+ Force Field
Synthesis of Cyclic Peptides with Agonist Activity for Melanocortin Receptors
Development of Potent and Selective Plasmin and Plasma Kallikrein Inhibitors and Studies on the Structure-Activity Relationship
Development of Plasmin Inhibitors and Their Effect on M1(Melanoma) and HT29 Cell Lines
Preparation of Highly Efficient Resin for Affinity Chromatography Employing Synthetic Specific Inhibitors : Further Studies on Purification of Plasma Kallikrein (PK)
Development of Plasmin-Selective Inhibitors and Studies of Their Structure-Activity Relationship
Design of Bifunctional Inhibitors for Enzymes in Coagulation-Fibrinolysis System : Synthesis of Plasmin Inhibitor and Evaluation of Their Inhibitory Effect
Design of Plasma Kallikrein Inhibitors : Functional and Structural Requirements of Plasma Kallikrein Inhibitors
Purification Method for Human Plasma Kallikrein by a New Affinity Chromatography
Purification of Plasma Kallikrein (PK) : Preparation of PK Specific Inhibitor-Polymer Conjugate and Its Application to Purification of PK
Design of Plasma Kallikrein Inhibitors
DEVELOPMENT OF A PLASMA KALLIKREIN SELECTIVE INHIBITOR
Structural Studies of [2',6'-Dimethyl-L-tyrosine^1]Endomorphin-2 Analogues Containing Proline Mimics
The Structure-Activity Relationship of [Dmt^1]Endomorphin-2 Derivatives
The Structure-Activity Relationship of the Opioidmimetics Containing 2(1H)-Pyrazinone Ring as a Linker and Observation of Deamination during Synthesis
Design of Opioidmimetics : Dimerization of 2', 6'-Dimethyl-L-Tyrosine
Degradation of a Novel Tripeptide, tert-Butoxycarbonyl-Tyr-Leu-Val-CH_2Cl, with Inhibitory Effect on Human Leukocyte Elastase in Aqueous Solution and in Biological Fluids

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