細菌内毒素の活性部位リピドA類の合成研究

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概要

• 論文の詳細を見る

• New Methodology for efficient synthesis of biologically active site components of bacterial lipopolysaccharides, lipid A and the related compounds was developed. From novel key intermediates bearing chemically differentiated one amino and four hydroxyl groups or two amino and six hydroxyl groups, lipid X, Y, glucosamine-4-phosphoric acid derivatives and lipid As were synthesized. These chemically synthesized compounds possess interesting biological activities.

• 社団法人 有機合成化学協会の論文

著者

• 清水 千賀子

  School Of Pharmaceutical Sciences University Of Shizuoka

• 阿知波 一雄

  静岡薬科大学薬品製造化学教室

• 池田 潔

  静岡薬科大学薬品製造化学教室

• 清水 千賀子

  静岡薬科大学薬品製造化学教室

関連論文

• Lipid A and Related Compounds. XI. New, Efficient Synthesis of Lipid X(Organic,Chemical)
• 4 Lipid X,YおよびSalmonella mutant Lipid Aの新合成
• A NEW METHODOLOGY FOR CHEMOSELECTION OF ONE AMINO AND FOUR HYDROXYL GROUPS OF GLUCOSAMINE DERIVATIVES AND ITS USE FOR SYNTHESIS OF LIPID X
• Neuraminic Acid and Related Compounds. V. Syntheses of Biologically Active Sialosyl-Glycerol Derivatives and Galactosyl-Glycerol Derivative
• SYNTHESES OF BIOLOGICALLY ACTIVE SIALOSYLGLYCEROL DERIVATIVES
• Neuraminic Acid and Related Compounds. I. : Syntheses of Biologically Active 4', 7', 8', 9'-Tetra-O-acetyl-sialyl- and Sialyl-(α2-6)-D-glucosamine-4-phosphate Analogues of Lipid A
• 細菌内毒素の活性部位リピドA類の合成研究
• ケイ素原子の特性を利用する環状付加反応
• 細菌内毒素の活性部位リピドA類の合成研究

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