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Division Of Organic Chemistry National Institute Of Health Sciences | 論文
- Characterization of the Cytotoxic Activity of Nitric Oxide Generating N-Nitroso Compounds
- Cyclization of 1-Aryl-1-nitroso-3-(2-pyridymethyl)ureas to 2-Aryl-5-(2-pyridyl)-2,4-dihydro-1,2,4-triazol-3-ones
- ADVANTAGES OF SIMPLIFIED QUANTITATIVE MORPHOMETRY USING STAGE GROUPING ANALYSIS OF SPERMATOGENIC CYCLE FOR EVALUATION OF THE TESTICULAR TOXICITY OF ETHYLENE-1, 2-DIMETHANESULFONATE IN RATS
- DIRECT TOXIC EFFECTS OF ETHYLENE-1, 2-DIMETHANESULFONATE (EDS) ON THE RAT EPIDIDYMIS
- Development of Des-Fatty Acyl-Polymyxin B Decapeptide Analogs with Pseudomonas aeruginosa-Specific Antimicrobial Activity
- 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
- Semi-synthesis of Polymyxin B (2-10) and Colistin (2-10) Analogs Employing the Trichloroethoxycarbonyl (Troc) Group for Side Chain Protection of α, γ-Diaminobutyric Acid Residues
- Chemical Conversion of Natural Polymyxin B and Colistin to Their N-Terminal Derivatives
- Semi-Synthesis of Polymyxin B-(2-10) Analogs Employing the Trichloroethoxycarbonyl (Troc) Group for Side Chain Protection of 2,4-Diaminobutyric Acid Residues
- Structure-Activity Relationships of Neuromedin U. V. Study on the Stability of Porcine Neuromedin U-8 at the C-Terminal Asparagine Amide under Mild Alkaline and Acidic Conditions
- 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
- Involvement of Electron Transfer in the Radical-scavenging Reaction of Resveratrol
- Computational Study on Secondary Structure of Oligopeptides Containing α,α-Disubstituted α-Amino Acids
- Controlling 3_-Helix and α-Helix of Short Peptides in the Solid State
- Controlling Helical Secondary Structures by Cyclic α,α-Disubstituted Amino Acids Having Side-Chain Chiral Centers
- Computational Study on Helical Structures of Oligopeptides Containing Chiral Cyclic α,α-Disubstituted α-Amino Acids
- Synthesis of Optically Active Cyclic α,α-Disubstituted Amino Acids by Enzymatic Kinetic Resolution and Conformational Analysis of Their Peptides
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