桜井満也 | Exploratory Chemistry Research, Sankyo Co., Ltd.,

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Studies of Human Immunodeficiency Virus Type 1 (HIV-1) Protease Inhibitors. III. Structure-Activity Relationship of HIV-1 Protease Inhibitors Containing Cyclohexylalanylalanine Hydroxyethylene Dipeptide Isostere
Studies of HIV-1 Protease Inhibitors. II.Incorporation of Four Types of Hydroxyethylene Dipeptide Isosteres at the Scissile Site of Substrate Sequences
Studies of HIV-1 Protease Inhibitors. I.Incorporation of a Reduced Peptide, Simple Aminoalcohol, and Statine Analog at the Scissile Site Substrate Sequences
Syntheses and Biological Activities of Renin Inhibitors Containign Statine Analogues
Asymmetric Synthesis of 2-Substituted-3-aminocarbonyl Propionic Acid
Studies on Peptides. CXLI. : Synthesis of a 42-Residue Peptide Corresponding to the Entire Amino Acid Sequence of Porcine GIP (Glucose-Dependent Insulinotropic Polypeptide)
Studies on Peptides. CXXXIX. : Solution Synthesis of a 42-Residue Peptide Corresponding to the Entire Amino Acid Sequence of Human Glucose-Dependent Insulinotropic Polypeptide (GIP)
Studies on Peptides. CXXXIII. : Synthesis and Biological Activity of Galanin, a Novel Porcine Intestinal Polypeptide
Studies on Peptides. CXXXI. Synthesis of Adrenorphin and Enkephalin Analogs
SYNTHESIS OF A 42 RESIDUE PEPTIDE CORRESPONDING TO THE ENTIRE AMINO ACID SEQUENCE OF HUMAN GIP

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