Search Results - "Okimura, Keiko"
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Examination of the Antimicrobial Peptide Myticalin A6 Active Site
Published in Biological & pharmaceutical bulletin (01-04-2021)“…In 2017, Leoni et al. reported myticalins as novel cationic linear antimicrobial peptides obtained from marine mussels. The authors focused on myticalin A6 (29…”
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2
Contribution of Each Amino Acid Residue in Polymyxin B3 to Antimicrobial and Lipopolysaccharide Binding Activity
Published in Chemical & Pharmaceutical Bulletin (01-03-2009)“…This study on the structure–activity relationship of polymyxin B, a cyclic peptide antibiotic, used sixteen synthetic polymyxin B3 analogs including alanine…”
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3
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
Published in Chemical & pharmaceutical bulletin (01-12-2007)“…Improved strategies for the chemical conversion of natural polymyxin B and colistin to their N-terminal analogs are reported. First, the protection of the side…”
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4
Development of Des-Fatty Acyl-Polymyxin B Decapeptide Analogs with Pseudomonas aeruginosa-Specific Antimicrobial Activity
Published in Chemical & pharmaceutical bulletin (01-04-2009)“…Twelve N-terminal analogs of des-fatty acyl-polymyxin B (Des-FA-[X1]-PMB, X=various amino acids or peptides) were synthesized and examined for their…”
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5
Chemical Conversion of Natural Polymyxin B and Colistin to Their N-Terminal Derivatives
Published in Bulletin of the Chemical Society of Japan (15-03-2007)“…The chemical conversions of natural polymyxin B and colistin, which are fatty-acylated cyclic decapeptides, to polymyxin (2–10) and colistin (2–10) derivatives…”
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Hydrolytic Cleavage of Pyroglutamyl-peptide Bond. V. Selective Removal of Pyroglutamic Acid from Biologically Active Pyroglutamylpeptides in High Concentrations of Aqueous Methanesulfonic Acid
Published in Chemical & pharmaceutical bulletin (01-06-2006)“…Application of aqueous methanesulfonic acid (MSA) for selective chemical removal of pyroglutamic acid (pGlu) residue from five biologically active…”
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7
The Contribution of the N-Terminal Structure of Polymyxin B Peptides to Antimicrobial and Lipopolysaccharide Binding Activity
Published in Bulletin of the Chemical Society of Japan (01-10-2004)“…To elucidate the N-terminal structure–activity relationships of polymyxin B peptides, seven polymyxin B component peptides, the structures of which having been…”
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8
Hydrolytic Cleavage of Pyroglutamyl-peptide Bond. V. Selective Removal of Pyroglutamic Acid from Biologically Active Pyroglutamylpeptides in High Concentrations of Aqueous Methanesulfonic Acid
Published in Chemical & Pharmaceutical Bulletin (2006)“…Application of aqueous methanesulfonic acid (MSA) for selective chemical removal of pyroglutamic acid (pGlu) residue from five biologically active…”
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9
HPLC Analysis of Fatty Acyl-Glycine in the Aqueous Methanesulfonic Acid Hydrolysates of N-Terminally Fatty Acylated Peptides
Published in Biological & pharmaceutical bulletin (01-08-2003)“…Acylation with long-chain fatty acids is a common modification at the N-terminal glycine residues of natural proteins. In this work, we performed HPLC analysis…”
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10
Development of Des-Fatty Acyl-Polymyxin B Decapeptide Analogs with Pseudomonas aeruginosa-Specific Antimicrobial Activity
Published in Chemical & Pharmaceutical Bulletin (2009)“…Twelve N-terminal analogs of des-fatty acyl-polymyxin B (Des-FA-[X1]-PMB, X=various amino acids or peptides) were synthesized and examined for their…”
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11
Regioselective Hydrolytic Cleavage of N-Terminal Myristoyl-peptide
Published in Chemical & pharmaceutical bulletin (1999)“…To develop a simple chemical deblocking method for Myr-Gly-peptide, we investigated the susceptibility and stability of the internal peptide linkages of model…”
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12
Study on Surfactin, a Cyclic Depsipeptide. II. Synthesis of Surfactin B2 Produced by Bacillus natto KMD 2311
Published in Chemical & pharmaceutical bulletin (1996)“…The total synthesis of surfactin B2, a cyclic depsipeptide isolated from Bacillus natto KMD 2311, was achieved to elucidate the absolute configuration of its…”
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13
Structure-Activity Relationships of Rat Neuromedin U for Smooth Muscle Contraction
Published in Chemical & pharmaceutical bulletin (1991)“…Rat neuromedin U (r-NMU) and its fragment peptide amides were synthesized by solid-phase methodology. Using a chicken crop smooth muscle contraction assay, the…”
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14
Contractile Activity of Porcine Neuromedin U-25 and Various Neuromedin U-Related Peptide Fragments on Isolated Chicken Crop Smooth Muscle
Published in Chemical & pharmaceutical bulletin (1992)“…Contractile activity of porcine neuromedin U-25 (p-NMU-25) and various neuromedin U (NMU) peptide fragment amides was examined on chicken crop smooth muscle…”
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15
Semi-synthesis of Polymyxin B (2-10) and Colistin (2-10) Analogs Employing the Trichloroethoxycarbonyl (Troc) Group for Side Chain Protection of [alpha],[gamma]-Diaminobutyric Acid Residues
Published in Chemical & pharmaceutical bulletin (01-12-2007)“…Improved strategies for the chemical conversion of natural polymyxin B and colistin to their N-terminal analogs are reported. First, the protection of the side…”
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16
Contribution of each amino acid residue in polymyxin B(3) to antimicrobial and lipopolysaccharide binding activity
Published in Chemical & pharmaceutical bulletin (01-03-2009)“…This study on the structure-activity relationship of polymyxin B, a cyclic peptide antibiotic, used sixteen synthetic polymyxin B(3) analogs including alanine…”
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17
Synthesis of Neurokinin B Analogs and Their Activities as Agonists and Antagonists
Published in Chemical & pharmaceutical bulletin (01-08-1987)“…Nine neurokinin B (NKB) related octapeptide analogs, substituted with Arg for His3, or Gly, D-Trp, D-Ala or D-Phe for Phe6, or Gly for Val7, or D-Trp or D-Ala…”
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18
Agonistic and Antagonistic Activities of Neuromedin U-8 Analogs Substituted with Glycine or D-Amino Acid on Contractile Activity of Chicken Crop Smooth Muscle Preparations
Published in Chemical & pharmaceutical bulletin (1991)“…To study the structure-actibity relationships of neuromedin U-8 (NMU-8) (H-Tyr-Phe-Leu-Phe-Arg-Pro-Arg-Asn-NH2) and to develop a NMU-8 antagonist, twenty-three…”
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