A Novel, Antimicrobially Active Analog of Gramicidin S without Amphiphilic Conformation
スポンサーリンク
概要
- 論文の詳細を見る
- 2006-06-25
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
-
SAWA Kenta
Department of Chemistry, Toho University
-
Sawa Kenta
Department Of Chemistry Toho University
-
Kikuchi Sho
Department Of Chemistry Toho University
-
Tamaki Makoto
Department Of Chemistry Toho University
-
Tamaki Makoto
Department Of Chemistry And Biomolecular Science Toho University
-
Uchida Yoshiki
Dep. Of Health And Nutrition Osaka Shoin Women's Univ.
-
Shindo Mitsuno
Department Of Health And Nutrition Osaka Shoin Women's 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
- 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
- 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.
- 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.
- 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.