佐々木有亮 | Tohoku College of Pharmacy

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概要

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著作論文

Synthesis of Carboxyl-Terminal Extension Analogs of Dermorphin and Evaluation of Their Opioid Receptor-Binding and Opioid Activities
Degradation of Deltorphins and Their Analogs by Rat Brain Synaptosomal Peptidases
Solid-Phase Synthesis and Opioid Activities of [D-Ala^2]Deltorphin II Analogs
Studies on Analgesic Oligopeptides. VII. Solid Phase Synthesis and Biological Properties of Tyr-D-Arg-Phe-βAla-NH_2 and Its Fluorinated Aromatic Amino Acid Derivatives
Solid Phase Synthesis and Opioid Receptor Binding Properties of Presumable Dermorphin Precursor Derivatives
Solid Phase Synthesis and Opioid Receptor Binding Activities of[D-Ala^2,D-Leu^5]Enkephalin Analogs Containing a Fluorinated Aromatic Amino Acid
Studies on Analgesic Oligopeptides. VI. : Further Studies of Synthesis and Biological Properties of Tripeptide Alkylamides, Try-D-Arg-Phe-X
Studies on analgesic Oligopeptides. V. : Structure-Activity Relationship of Tripeptide Alkylamides, Tyr-D-Arg-Phe-X
Studies on Analgesic Oligopeptides. IV. Synthesis and Analgesic Activity of N-Terminal Shorter Analogs of [D-Arg^2] Dermorphin and Des-Tyr^1-Dermorphin Analogs
Studies on Analgesic Oligopeptides. III. Synthesis and Analgesic Activity after Subcutaneous Administration of [D-Arg^2] dermorphin and Its N-Terminal Tetrapeptide Analogs
Studies on Analgesic Oligopeptides. II. Structure-Activity Relationship among Thirty Analogs of a Cyclic Dipeptide, Cyclo (-Tyr-Arg-)
Structure and Analgesic Activity Relationship of Cyclo-Tyrosyl-Arginyl and Its Three Stereoisomers
Acetic Acid-Catalyzed Diketopiperazine Synthesis
Selective Cleavage of tert-Butyloxycarbonyl Protecting Group with Dilute Organic Sulfonic Acid without Decomposition of Tryptophan Residue
The γ-Phenacyl and γ-p-Nitrobenzyl Esters to Minimize Side Reactions during Treatment of Glutamyl Peptides with Hydrogen Fluoride-Anisole Mixture
Studies on Encephalitogenic Fragments of Myelin Protein. III. Synthesis of H-Arg-Phe-Ser-Trp-Gly-Ala-Glu-Gly-Asn-Arg-OH as an Analog of Encephalitogenic Decapeptide
Tactics for Simplification of Purification Process in the Solid Phase Peptide Synthesis
Studies on Encephalitogenic Fragments of Myelin Protein. I. Synthesis of Tryptophan-containing Fragments
Synthesis and Opioid Activities of [D-Leu^8]Dynorphin(1-8) Analogs Containing a Reduced Peptide Bond, Ψ(CH_2NH)
The β-Phenacyl and β-p-Nitrobenzyl Esters to Suppress Side Reactions during Treatment of Aspartyl Peptides with Hydrogen Fluoride
Studies on Encephalitogenic Fragments of Myelin Protein. IV. Synthesis of Glycine Analogs of Tryptophan-containing Fragment
Studies on Encephalitogenic Fragments of Myelin Protein. II. Solid Phase Synthesis of Tryptophan-containing Decapeptide

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