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CHEMOSYNTHESIS OF CYCLIC LIPOPEPTIDE COMPOUND AND CYCLIC LIPOPEPTIDE
CHEMOSYNTHESIS OF CYCLIC LIPOPEPTIDE COMPOUND AND CYCLIC LIPOPEPTIDE
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机译:环脂肽化合物和环脂肽的化学合成
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摘要
PROBLEM TO BE SOLVED: To efficiently synthesize the subject compound by binding an amino acid, etc., having plural functional groups bound to lipids to a carrier, carrying out a chain-extending reaction by the second functional group, cyclizing the third functional group of the starting material with the terminal group, and separating the carrier therefrom. ;SOLUTION: This chemosynthetic method for a cyclic lipopeptide compound comprises the step of forming a carrier-bound body by binding the first functional group F1a of a starting material of an amino acid A1 or a compound having two or more functional groups binding to lipid components and the amino acid A1 to a carrier, the step of carrying out successive extension reaction of amino acids at the part of the second functional group F1b of the carrier- bound starting material, and joining one or more 3-functional amino acid to the reaction when the starting material has only two functional groups, the step of cyclizing the extended reaction product by binding the functional group Fn of the growing end amino acid An of the extended reaction product to the third functional group F1c of the starting material or the third functional group Fx of the amino acid residue Ax and the step of separating the obtained cyclic compound from the carrier and further binding a lipid component to the obtained cyclic product if the cyclic product having no lipid component bound thereto to provide the objective cyclic lipopeptide compound.;COPYRIGHT: (C)1998,JPO
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机译:解决的问题:通过将具有多个与脂质结合的官能团的氨基酸等结合到载体上,通过第二官能团进行扩链反应,环化第三官能团来有效地合成标题化合物。带有端基的起始材料,并从中分离载体。 ;解决方案:这种环状脂肽化合物的化学合成方法包括通过结合氨基酸A 1 <的起始材料的第一官能团F 1a Sub>形成载体结合体的步骤。 / Sub>或具有两个或多个与脂质成分结合的官能团以及将氨基酸A 1 Sub>与载体结合的化合物,在第二个部分进行氨基酸连续延伸反应的步骤与载体结合的起始原料的官能团F 1b Sub>,并且当起始原料仅具有两个官能团时,将一个或多个3-官能氨基酸结合到反应中,该步骤是将扩展的反应产物环化通过将扩展的反应产物的生长末端氨基酸A n Sub>的官能团F n Sub>与该反应产物的第三官能团F 1c Sub>结合残基A x Sub>的起始原料或第三官能团F x Sub>和分离步骤如果没有脂质成分结合的环状产物与载体结合,则从载体上获得环状化合物,并将脂质成分进一步结合到环状产物上,从而得到目标环状脂肽化合物。版权所有:(C)1998,日本特许厅
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