Synthesis of Surfactin B_2 produced by Bacillus natto KMD 2311
スポンサーリンク
概要
- 論文の詳細を見る
- 1995-10-01
著者
-
OHKI Kazuhiro
Faculty of Pharmaceutical Sciences, Hokuriku University
-
OKIMURA Keiko
Faculty of Pharmaceutical Sciences, Hokuriku University
-
Ohnishi Kuniharu
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Ohnishi Kuniharu
北陸大学 薬学部
-
Ohki K
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Ohki Kazuhiro
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Okimura Keiko
Faculty Of Pharmaceutical Sciences Hokuriku University
-
NAGAI Satoo
Faculty of Pharmaceutical Sciences, Hokuriku University
-
KAIZAWA Naohito
Faculty of Pharmaceutical Sciences, Hokuriku University
-
KANATOMO Shoichi
Faculty of Pharmaceutical Sciences, Hokuriku University
-
Kaizawa N
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Kaizawa Naohito
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Kanatomo S
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Kanatomo Shoichi
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Nagai Satoo
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Nagai S
Faculty Of Pharmaceutical Sciences Hokuriku University
-
Nagai Sotoo
北陸大学 薬学部
-
Natori S
Graduate School Of Pharmaceutical Sciences The University Of Tokyo
関連論文
- 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
- Synthesis of Surfactin B_2 produced by Bacillus natto KMD 2311
- Hydrolytic Cleavage of Pyroglutamyl-peptide Bond. V. Selective Removal of Pyroglutamic Acid from Biologically Active Pyroglutamylpeptides in High Concentrations of Aqueous Methanesulfonic Acid
- Isolation and Structure Determination of [Ile^7]- and [Ser^2]-Polymyxin B_1
- Antimicrobial Activity of Polymyxin B_3 Analogs modified at the Hydrophobic Amino Acids
- HPLC Analysis of Fatty Acyl-Glycine in the Aqueous Methanesulfonic Acid Hydrolysates of N-Terminally Fatty Acylated Peptides(Analytical Biochemistry)
- HPLC Analysis of Fatty Acylglycine in the Hydrolysates of N-Terminally Blocked Peptides by Fatty Acids
- Regioselective Hydrolytic Cleavage of N-Terminal Myristoyl-peptide
- Regioselective Hydrolysis of Formyl-peptide in Aqueous Methanesulfonic Acid
- Study on Surfactin, a Cyclic Depsipeptide. II. Synthesis of Surfactin B_2 Produced by Bacillus natto KMD 2311
- Enzymatic Degradation of Rabbit Neuromedin U-25 Related Peptides
- Chemical Conversion of Natural Polymyxin B to Polymyxin B Nonapeptide Derivatives
- Synthesis of Neurokinin B Analogs and Their Activities as Agonists and Antagonists(Organic,Chemical)
- Highly Selective Hydrolytic Cleavage of Pyroglutamyl-Peptide Bond
- Regioselective Cleavage of Myristoyl-Peptide in Acidic Solution
- Synthesis and Antimicrobial Activity of Polymyxin B Component Peptides
- Synthesis of Cyclic Peptide Antibiotic Polymyxin B Derivatives
- B-12-3 The Constitution of Enmein, a Bitter Principle of Isodon trichocarpus KUDO(Terpenoids)
- Hydrolytic Cleavage of Pyroglutamyl-Peptide Bond. II. Effects of Amino Acid Residue Neighboring the pGlu Moiety
- HIGHLY SELECTIVE CLEAVAGE OF PYROGLUTAMYL-PEPTIDE BOND IN CONCENTRATED HYDROCHLORIC ACID
- Decomposition of pyroglutamyl-Peptides in Dilute Acid
- Inhibition Effects of 5-S-Glutahionyl-N-β-alanyl-L-dopa Analogues against Src Protein Tyrosine Kinase
- Different Inhibitory Effects of 5-S-Glutathionyl-β-alanyl-L-dopa (5-S-GA-L-D) Analogues on Autophosphorylation and Substrate Phosphorylation of Src Protein Tyrosine Kinase
- Selective Inhibition of Src Protein Tyrosine Kinase by Analogues of 5-S-Glutathionyl-β-alanyl-L-dopa
- Antimicrobial Activity of Various Aminocyclohexylcarbonyl-polymyxin B (2-10) Derivatives
- Hydrolytic Cleavage of Pyroglutamyl-Peptide Bond. IV. Highly Selective Cleavage of Thyrotropin Releasing Hormone (TRH) in Aqueous Methanesulfonic Acid
- Hydrolytic Cleavage of Pyroglutamyl-peptide Bond. III. A Highly Selective Cleavage in 70% methanesulfonic Acid