Syntheses of Active Gramicidin S Analogues without Amphiphilic Conformation. II

スポンサーリンク

概要

• 論文の詳細を見る
• 2008-03-01

著者

• UCHIDA Yoshiki

  Department of Food Science and Nutrition, Osaka Shoin Women's University

• SHINDO Mitsuno

  Department of Food Science and Nutrition, Osaka Shoin Women's University

• Shindo Mitsuno

  Department Of Food Science And Nutrition Osaka Shoin Women's University

• Uchida Yoshiki

  Department Of Applied Chemistry Faculty Of Engineering Osaka City University

• TAMAKI Makoto

  Department of Chemistry, Faculty of Science, Toho University

• KIKUCHI Sho

  Department of Chemistry, Toho University

• Kikuchi Sho

  Department Of Chemistry Toho University

• Sasaki Ichiro

  Department Of Chemistry Toho University

• Tamaki Makoto

  Department Of Chemistry Toho University

• Tamaki M

  Department Of Chemistry Toho University

• Tamaki Makoto

  Department Of Chemistry And Biomolecular Science Toho University

• ITAKURA Ryohei

  Department of Chemistry, Toho University

• Uchida Yoshiki

  Dep. Of Health And Nutrition Osaka Shoin Women's Univ.

• Sasaki Ichiro

  Department Of Aeronautics University Of Tokyo

• Shindo Mitsuno

  Department Of Health And Nutrition Osaka Shoin Women's University

• Itakura Ryohei

  Department Of Chemistry Toho University

• TAMAKI Makoto

  Department of Chemistry, Toho University

関連論文

• Contribution of Each Amino Acid Residue in Polymyxin B_3 to Antimicrobial and Lipopolysaccharide Binding Activity
• Des-Fatty Acyl-Polymyxin B Decapeptide Analogs with Antimicrobial Activity Specifically against Pseudomonas aeruginosa
• Chemical Conversion of Natural Polymyxin B and Colistin to Their N-Terminal Derivatives
• Antimicrobial Activity of Des-Fatty Acyl-Polymyxin B Decapeptide N-Terminal Analogs
• The Contribution of the N-Terminal Structure of Polymyxin B Peptides to Antimicrobial and Lipopolysaccharide Binding Activity
• Antimicrobial Activity of Polymyxin B_3 Analogs modified at the Hydrophobic Amino Acids
• Chemical Conversion of Natural Polymyxin B to Polymyxin B Nonapeptide Derivatives
• Antibacterial Activity of Short Peptides Based on Pleurocidin and Their Interaction with Phospholipid Membranes
• Synthesis and Biological Activities of Indolicidin Analogs (III)
• Antibacterial Activity of Short Peptides Based on Pleurocidin and Their Interaction with Phospholipid Membranes
• Synthesis and Biological Activities of Indolicidin Analogs (II)
• Synthesis and Biological Activities of Indolicidin Analogs
• Nitrated and Oxidized Products of a Single Tryptophan Residue in Human Cu,Zn-Superoxide Dismutase Treated with Either Peroxynitrite-Carbon Dioxide or Myeloperoxidase-Hydrogen Peroxide-Nitrite
• A Novel Active Analogue of Gramicidin S with Smaller Ring Size
• Syntheses of Cyclic Peptides Containing 4-cis-Amino-L-Proline
• Synthesis and Properties of Gramicidin S Analogues with Smaller Ring Size
• Biomimetic Cyclization of Linear Peptides Related to Gramicidin S with Several Lengths on Solid Support
• Biomimetic Synthesis of Gramicidin S, Direct Formation of the Antibiotic from Pentapeptides Related to Gramicidin S on Solid Support
• Synthesis and Antimicrobial Activity of Polymyxin B Component Peptides
• Synthesis of Cyclic Peptide Antibiotic Polymyxin B Derivatives
• Structure-Activity of Antibacterial Peptide Indolicidin and Analogs
• Antibacterial Activity of the Mammalian Host Defense Peptide, Indolicidin, and Its Fragments
• Solvent-Dependent Conformations of Cyclic Tetrapeptide. II
• γ-Functional Prolines Based on Naturally Occurred Hydroxyproline. III
• γ-Functional Prolines Based on Naturally Occurring Hydroxyproline. II
• Novel Des-Fatty Acyl-Polymyxin B Derivatives with Pseudomonas aeruginosa-Specific Antimicrobial Activity
• Design and Synthesis of Arg-Containing Peptides Having Various Secondary Structures and Their Biological Activities
• Phytochelatins inhibit the metal-induced aggregation of α-crystallin(PLANT BIOTECHNOLOGY)
• Syntheses and Properties of Gratisin Analogues Containing Ala Residue
• Syntheses of Gramicidin S Analogues Consisting of Eleven Amino Acid Residues
• Conformation of Cyclic Tetrapeptides Containing Two Pro Residues
• Syntheses of Gramicidin S Analogues Containing Cis-D-Phe-Pro Peptide Bond
• Novel Antimicrobial Gratisin Analogues Containing Various D-Amino Acid Residues in Place of D-Tyr Residues
• Syntheses of Active Gramicidin S Analogues without Amphiphilic Conformation. II
• A Novel Polycationic Analogue of Gratisin with Antibiotic Activity against both Gram-positive and Gram-negative Bacteria
• Syntheses of Active Gramicidin S Analogs without Amphiphilic Conformation
• A Novel, Antimicrobially Active Analog of Gramicidin S without Amphiphilic Conformation
• Synthesis and Properties of Cyclic Peptides Containing α,δ-Diaminovaleric Acid Linker
• Relationship between the Cyclization and Conformation of Pentapeptide Active Esters Related to Gramicidin S Having No Protecting Group on the Side Chain of the Ornithine Residue
• Cyclization of Hexapeptide Active Esters Related to Gratisin Having No Protecting Group on the Side Chain of Ornithine Residue
• Practical Synthesis of 4-cis Hydroxy-L-Proline
• Polymerization of Isoprene with Ni(acac)_2-Methylaluminuxane Catalyst
• Conformational Analysis of a Peptide Antibiotic "Gratisin"
• Cyclization of Pentapeptide Related to Gramicidin S without Protection of δ-Amino Group of the Ornithine Residue on Solid Support
• An Improved Czochralski Technique for Growing Single Crystals with High Homogeneity
• γ-Functional Prolines Based on Naturally Occurring Hydroxyproline.
• Conformational Analysis of a Peptide Antibiotic "Gratisin". II
• Syntheses and Conformational Analyses of Cyclic Peptides Containing 4-cis-Amino-L-Proline. II
• Antimicrobially Active Analogues of Gramicidin S Having Fatty Acyl Moiety
• Syntheses of Novel Cyclic Undecapeptides Related to Gramicidin S with D-Phe-X-Pro Sequences
• Rotating Stall in Blade Rows Operating in Shear Flow : 1st Report : The Case of Shear Flow with Linear Velocity Profile
• Hybrid Analogues of Gramicidin S and Gratisin
• Syntheses and Properties of Cyclic Tetrapeptides Containing α, δ-Diaminovaleric Acid and α, ε-Diaminocaproic Acid Linkers
• Polycationic Gramicidin S Analogues with Both High Antibiotic Activity and Very Low Hemolytic Activity
• Synthesis of Novel Fatty-Acyl Gratisin Derivatives
• Design and syntheses of gramicidin S analogs, cyclo(-X-Leu-X-D-Phe-Pro-)_2 (X=His, Lys, Orn, Dab and Dap)
• Gramicidin S analogs having six basic amino acid residues
• Novel Cycloundecapeptides Related to Gramicidin S with Both High Antibiotic Activity and Low Hemolytic Activity
• Synthesis and properties of gramicidin S analogs containing D-Phe-L-Pro-D-Val or L-Phe-L-Pro-D-Val sequences in place of D-Phe-L-Pro-L-Val sequence in the .BETA.-turn part of the antibiotic.
• Four Cases of Graves' Disease which Developed after Painful Hashimoto's Thyroiditis
• Studies on the Secondary Structure of Bradykinin in Aqueous Solution. Syntheses, Circular Dichroism Spectra, and Biological Activities of Bradykinin Analogs Containing 5-Aminovaleric Acid Residue.
• Deoximation of oxime O-acetates, oximes, and oxime ethers by nonacarbonyldiiron or pentacarbonyliron. An electronic effect for the N-O bond cleavage.
• Possible interpretation of inactivity of novel gramicidin S analogs by CD spectral analysis of tetrapeptide derivatives related to the analogs.
• Synthesis and properties of gramicidin S analogs containing D-Lys residue in place of Orn residue.

もっと見る 閉じる

スポンサーリンク