玉村啓和 | Faculty of Pharmaceutical Sciences, Kyoto University

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著作論文

Solution-Phase Synthesis of an Anti-human Immunodeficiency Virus Peptide, T22 ([Tyr^, Lys^7]-Polyphemusin II), and the Modification of Trp by the p-Methoxybenzyl Group of Cys during Trimethylsilyl Trifluoromethanesulfonate Deprotection
Molecular Parameters for the Anti-Human Immunodeficiency Virus Activity of T22 ([Tyr^, Lys^7]-Polyphemusin II)
Synthesis of Protegrin-Related Peptides and Their Antibacterial and Anti-human Immunodeficiency Virus Activity
Synthesis of Optically Pure 2-Aziridinemethanols : Versatile Synthetic Building Blocks
Antimicrobial Activity and Conformation of Tachyplesin I and Its Analogs
Acceleration of the N^α-Deprotection Rate by the Addition of m-Cresol to Diluted Methanesulfonic Acid and Its Application to the Z(OMe)-Based Solid-Phase Syntheses of Human Pancreastatin-29 and Magainin 1

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