脇道典 | SEIKAGAKU Corporation

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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
HIV-cell Fusion Inhibitors Targeted to the HIV Second Receptor : T22 and Its Downsized Analogs with High Activity
Design, Synthesis and Activity of Shortened Analogs of an Anti-HIV Peptide, T22
Molecular Size of an Anti-HIV Peptide, T22, Can Be Reduced without Loss of the Activity
Identification of a Polyphemusin Analog(T22)-Zn(II) Complex by Mass Spectrometric Analysis and Its Anti-HIV Activity
Identification of Binding Proteins of an Anti-HIV Peptide, T22

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