Akaji K | Kyoto Pharmaceutical Univ. Kyoto Jpn

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概要

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著作論文

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
Design of HIV Protease Inhibitors Based on the Transition State Analogue Concept
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
SYNTHESES AND STRUCTURE-ACTIVITIES RELATIONSHIPS OF SMALLSIZED ATRIAL NATRIURETIC PEPTIDE (ANP) DERIVATIVES WITH POTENT ACTIVITY
SYNTHESES AND STRUCTURE-ACTIVITY RELATIONSHIPS OF SMALL-SIZED ATRIAL NATRIURETIC PEPTIDE (ANP) DERIVATIVES
Solid Phase Synthesis of a Mercaptoamide Peptide Using New Linkers
SYNTHESES OF CYSTINE-PEPTIDES BY A NEW DISULPHIDE BOND FORMING REACTION
SYNTHESES AND BIOLOGICAL ACTIVITIES OF SEVERAL NEWLY ISOLATED NATRIURETIC PEPTIDES
Convergent Synthesis of Dolastatin 15 by Solid Phase Coupling of N-methylamino Acid
Total Synthesis of (-)-Mirabazole B Using a Chloroimidazolidium Reagent, CIP
Efficient Synthesis of Alamethicin using a Newly Developed Coupling Reagent, CIP
Efficient Coupling of Dialky Amino Acid Using a Chloro Imidazolidium Reagent, CIP

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