Semi-Synthesis of Polymyxin B-(2-10) Analogs Employing the Trichloroethoxycarbonyl (Troc) Group for Side Chain Protection of 2,4-Diaminobutyric Acid Residues
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概要
- 論文の詳細を見る
- 2007-03-01
著者
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SATO Yuki
Faculty of Agriculture, Niigata University
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Sato Y
Faculty Of Pharmaceutical Sciences Hokuriku University
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Sato Y
Division Of Organic Chemistry National Institute Of Health Sciences
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OHKI Kazuhiro
Faculty of Pharmaceutical Sciences, Hokuriku University
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OKIMURA Keiko
Faculty of Pharmaceutical Sciences, Hokuriku University
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OHNISHI Kuniharu
Faculty of Pharmaceutical Sciences, Hokuriku University
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SAKURA Naoki
Faculty of Pharmaceutical Sciences, Hokuriku University
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Ohnishi Kuniharu
Faculty Of Pharmaceutical Sciences Hokuriku University
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Ohnishi Kuniharu
北陸大学 薬学部
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Ohki K
Faculty Of Pharmaceutical Sciences Hokuriku University
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Ohki Kazuhiro
北陸大学 薬学部
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Ohki Kazuhiro
Faculty Of Pharmaceutical Sciences Hokuriku University
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Okimura K
Faculty Of Pharmaceutical Sciences Hokuriku University
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Okimura Keiko
北陸大学 薬学部
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Okimura Keiko
Faculty Of Pharmaceutical Sciences Hokuriku University
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佐倉 直樹
北陸大・薬
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Sakura N
Hokuriku Univ. Kanazawa Jpn
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Sakura Naoki
北陸大学 薬 生物活性
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Sakura Naoki
北陸大学 薬学部
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Sakura Naoki
Faculty Of Pharmaceutical Sciences Hokuriku University
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Sato Yukiko
Division Of Organic Chemistry National Institute Of Health Sciences
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Sato Yuki
Faculty Of Agriculture Niigata University
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- 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
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