北川幸己 | Faculty of Pharmaceutical Sciences, Kyoto University

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著作論文

Studies on Peptides. Application of Trifluoromethanesulphonic Acid as a Deblocking Reagent to the Synthesis of Neurotensin
Solution Synthesis of Human Peptide YY (hPYY)
Solution Synthesis of Human Neuropeptide Y (hNPY)
Studies on Peptides. CXXXVI. : Solution-Phase Synthesis of a 37-Residue Peptide Amide Corresponding to the Entire Amino Acid Sequence of Human Calcitonin Gene-Related Peptide (hCGRP)
Synthesis and Activity of a newly Isolated Analgesic Pentapeptide, Neo-kyotorphin
Synthesis and Analgesic Activity of Neo-kyotorphin Analogs
Studies on Peptides. XLIII. Synthesis of Two Protected Peptides Related to the C-Terminal Portion of the Basic Trypsin Inhibitor from Bovine Pancreas (Kunitz and Northrop)
A Deblocking Method using Thioether-Sulfonic Acid Systems. Application to the Synthesis of Met-Enkephalin
Studies on Peptides. CXXXV. : Preparation of Seven Peptide Fragments for the Synthesis of Human Calcitonin Gene-Related Peptide (hCGRP)
Enzyme Immunoassay of a Substance P-like Immunoreactive Substance in Human Plasma and Saliva
Facile Reduction of Methionine Sulfoxide with Sulfur Trioxide/Iodide Ion System
Solution Syntheses of Two Enkephalin-Containing Peptides, Peptide E and Dynorphin(1-24), Using N^-(2,4,6-Triisopropylphenylsulfonyl)tryptophan
Alternative Synthesis of Porcine Secretin and Apparent Autolysis of the Product
Suppressing Effect of Thioanisole on a Side Reaction during the Acidolytic Cleavage of Protecting Groups of Tyrosine
Studies on Peptides. LVIII. Synthesis of Tyr^1-Substance P

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