New Phosphoryl Protecting Groups for Synthesis of Phosphopeptides by Boc Method

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概要

• 論文の詳細を見る
• 1995-10-01

著者

• Saruta Kunio

  Department Of Chemistry Faculty Of Science And Technology Kinki University

• AIMOTO Saburo

  Institute for Protein Research, Osaka University

• NAKAJIMA Kiichiro

  Peptide Institute Inc., Protein Research Foundation

• WAKAMIYA Tateaki

  Faculty of Science and Technology, Kinki University

• YOSHIZAWA KUMAGAYE

  Peptide Institute, Inc., Protein Research Foundation

• YOSHIZAWA-KUMAGAYE Kumiko

  Peptide Institute Inc., Protein Research Foundation

• Kusumoto Shoichi

  Faculty Of Science Osaka University

• Nakajima Kiyohiko

  Aichi University Of Education Igaya

• Kusumoto S

  Department Of Chemistry Graduate School Of Science Osaka University

• Aimoto Saburo

  Institue For Protein Research Osaka University

• Aimoto Saburo

  Institude For Protein Research Osaka University

• TOGASHI Ryusaku

  Department of Chemistry, Faculty of Science and Technology, Kinki University

• TOGASHI Ryusaku

  Faculty of Science and Technology, Kinki University

• SARUTA Kunio

  Faculty of Science, Osaka University

• Yoshizawa-kumagaye Kumiko

  Peptide Institute Inc. Protein Research Foundation

• Wakamiya T

  Faculty Of Science And Technology Kinki University

• Wakamiya Tateaki

  Faculty Of Science And Technology Kinki University

• Kamagaye Kumiko

  Saito Research Center Peptide Institute Inc.

• Togashi Ryusaku

  Department Of Chemistry Faculty Of Science And Technology Kinki University

• Wakamiya Tateaki

  Faculty Of Science And Engineering Kinki University

• Nakajima Kiichiro

  Peptide Institute Inc. Protein Research Foundation

• Yoshizawa-kumagaye Kumiko

  Saito Research Center Peptide Institute Inc.

関連論文

• Development of a Method for the Preparation of Peptide Thioesters by an Fmoc Solid Phase Method
• Synthesis of Cysteine-Containing Polypeptide Using a Peptide Thioester Containing a Cys(Acm) Residue
• Polypeptide Synthesis Using Cys(Acm)-Containing Peptide Thioester as Building Block
• Synthesis of a Partial Sequence of Site-Specifically Methylated Histone H3
• Peptide Purification Using α-Ketoacyl Group Chemistry
• Preparation of a Peptide Thioester by the Fmoc-Solid Phase Method via an On-Resin N-S Acyl Shift
• Chemical Ligation Using a Photoremovable Auxiliary
• Conformational Analyses of The P-type Calcium Channel Blocker, ω-Agatoxin-TK
• Synthesis of Optically Active β-[4-(^B)Borono-2,6-difluorophenyl]alanine and Its Evaluation as a Boron Carrier for BNCT
• In Vitro and Vivo Evaluation of Fluorinated p-Boronophenylalanine Derivatives as Boron Carrier and MRI Probe
• Syntheses and Biological Activities of Fluorescent Labeled Analogs of Acylpolyaminetoxin NPTX-594 Isolated from the Venom of Madagascar Joro Spider
• Synthesis and Evaluation of the Compounds Containing ^B and ^F Atoms as Boron Carrier and Imaging Agent
• Study on the Structure Activity Relationship of a Phytosiderophore, Mugineic Acid
• Synthesis and Biological Activity of Fluorescent Labeled Analogs of the Spider Toxin NPTX-594
• Structural Study of Novel Acylpolyaminetoxins from the Venom of Nephila clavipes, a Brazilian Joro Spider
• Study of the Fluorine- and Boron-10 Containing Compounds toward MRI and BNCT
• Study on the Structure Activity Relationships of NPTX-594, a Spider Toxin Belonging to the Type-B Acylpolyamine Structure
• Total Synthesis of the Novel Spider Toxin NPTX-594 from Nephila madagascariencis^1
• Study on Structure Activity Relationships of Spider Toxins with Generalized Acylpolyamine Structure of Type-B
• Study on the Relationship between Structure and Metal Complexation Ability of Mugineic Acid
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• Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii and Determination of Its Disulfide Linkage
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• 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
• Synthesis of a Phosphorylated Polypeptide by a Thioester Method
• SYNTHESIS OF A MOLT - INHIBITING HORMONE IN THE AMERICAN CRAYFISH PROCAMBARUS CLARKII BY NATIVE CHEMICAL LIGATION
• Synthesis of Cysteine-Containing Polypeptide Using Peptide Thioester : Preparation of a Molt-Inhibiting Hormone from the American Crayfish, Procambarus clarkii
• Design and Synthesis of Peptides Passing through the Blood-Brain Barrier
• Study on Peptide Transport across Tissue Cell Menbrane by Adsorptive-Mediated Transcytosis
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• Peptide Ligation Using a Building Block Having a Cysteinyl Prolyl Ester (CPE) Autoactivating Unit at the Carboxy Terminus
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• Peptide Ligation That Involves an Intramolecular N to S Acyl Shift Reaction
• Generation of an S-Peptide via an N-S Acyl Shift Reaction in a TFA Solution
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• Analysis of bile acid glutathione thioesters by liquid chromatography/electrospray ionization-tandem mass spectrometry
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• Synthesis of ρ-Boronophenylalanine-Containing Peptides for Boron Neutron Capture Therapy of Cancer Cells
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• Study Directed toward the Analysis of Interaction between the Spider Toxin NPTX-594 and Glutamate Receptors
• Synthesis of β-Peptides utilizing C-Glycosyl β-Amino Acid
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• Characterization of the Ligand-Binding Specificities of Integrin α3β1 and α6β1 Using a Panel of Purified Laminin Isoforms Containing Distinct α Chains
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• Preparations of N^α-Fmoc-0-[(Benzyloxy)hydroxyphosphinyl] β-Hydroxy α-Amino Acid Derivatives
• New Phosphoryl Protecting Groups for Synthesis of Phosphopeptides by Boc Method
• Preparation of Phosphoamino Acid Derivatives with Acid Stable O-Phosphono-Protection for the Boc-Mode Solid-Phase Synthesis of Phosphopeptides^
• An Efficient Procedure for Solid-Phase Synthesis of Phosphopeptides by the Fmoc Strategy
• Stereoselective Synthesis and Evaluation of HTLV-1 Protease Inhibitors
• Preparation of Partially Protected Peptide Thioesters Containing a Cysteine Residue and Their Segment Condensation
• Study on Solid-Phase Synthesis of Compounds, Containing Hydroxyamino Acids or Saccharides, by Taking Advantage of the Characteristics of Glutamic Acid
• Study on Peptides Inhibiting the Activation of Gelatinase A (MMP-2)
• SOLID PHASE SYNTHESIS OF THE ANTIBACTERIAL GLYCOPEPTIDE, FORMAECIN USING BOC-STRATEGY
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• Regeneration to the native form of hen egg-white lysozyme from its protected derivatives.

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