Hybrid Analogues of Gramicidin S and Gratisin
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概要
- 論文の詳細を見る
- 2004-09-25
著者
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Tamaki Makoto
Department Of Chemistry Toho University
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Tamaki M
Department Of Chemistry Toho University
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Tamaki Makoto
Department Of Chemistry And Biomolecular Science Toho University
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TAMAKI Makoto
Department of Chemistry, Toho University
関連論文
- 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
- 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
- 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
- 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
- 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.