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Department Of Medicinal Chemistry Graduate School Of Medical Science Kyoto Prefectural University Of | 論文
- Synthesis and Activity of a New Type of Anti-HIV Agents, Conjugate of HIV Protease Inhibitor with Reverse Transcriptase Inhibitor
- Synthesis of an HIV-1 Protease Analogue by the Chemoselective Ligation Method Using a New Disulfide Type Linker
- Small-sized HIV Protease Inhibitors Containing Allophenylnorstatine as a Substrate Transition-state Mimic
- Synthesis of Transmembrane Protein, F_1F_0 ATP Synthase Subunit c, by Thioester Method
- Synthesis of HIV Protease Dipeptide Inhibitors and Prodrugs
- The N-Terminal Helical Segments Modulate Structure and Lipid Interaction of Human Apolipoprotein A-I
- Studies on Structure-Activity Relationship of HTLV-1 Protease Inhibitors
- Solid-Phase Syntheses of Olefin-Containing Protease Inhibitors Using Horner-Emmons Reaction
- Synthesis of Olefin-Containing Cyclic Peptide Library Using the Solid-Phase Horner-Emmons Reaction
- Solid-Phase Peptide Synthesis Using N^α-Fmoc(2-F)-Amino Acid and Its Application to the Synthesis of Phosphorylated Peptide Thioesters
- Total Synthesis of Human T-cell Leukemia Virus Type-1 Protease via the Thioester Method
- Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii and Determination of Its Disulfide Linkage
- Synthesis of Phosphorylated Polypeptide Using an Expressed Peptide as a Building Block
- Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii, and Determination of the Location of Its Disulfide Linkages^1
- Use of an Expressed Peptide Segment as a Building Block for the Preparation of Phosphorylated Polypeptide via the Thioester Method
- Studies on N^〈in〉-Protecting Groups during the Synthesis of Trp : Containing Cystine Peptide by Silyl Chloride Sulfoxide Method
- A Reductive Acidolysis Final Deprotection Strategy in Solid Phase Peptide Synthesis Based on Safety-Catch Protection
- Synthesis of Human C-Type Natriuretic Peptide 22 Using Chlorotrityl Resin and Tetrafluoroboric Acid Deprotection
- Structure Activity Relationship Study of SARS Coronavirus 3CL Protease Inhibitors with an Electrophilic Aryl Ketone Structure
- Development of Stimulus Responsive Thiol Releasing System for Controlling Activity of Cysteine Protease