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八肽胆囊收缩素(CCK8)的人工合成
The Synthesis of Octapeptide Choiecystokinin
【摘要】 本文报道了用液相法合成八肽胆囊收缩素(H-Asp-Tyr(SO3H)-Met-Gly-Trp-Met-Asp-Phe-NH2,ccK8)。先分别合成C-端四肽和N-端四肽,然后缩合成八肽,并用温和的乙酰硫酸吡啶盐(PAS)法使其酪氨酸的酚羟基硫酯化。根据其氨基酸组成,层析行为和生物活性等证实产物为纯品。
【Abstract】 In this paper the synthesis of the octapeptide Cholecystokinin, H-Asp-Tyr (SO3H)-Met-Gly-Trp-Met-Asp-Phe-NH2, by the method of liquid phase condensation was described. C-terminal tetrapeptide and N-terminal tetrapeptide have been synthesized first using the liquid phase method and then coupled successively. The phenolic hydroxl of Tyr residue in CCK-8 is sulfated by a mild reagent, pyridinium acetylsul-fate (PAS).A homogeneous synthetic CCK-8 was finally identificated with respect to its amino acid composition, chromatographic behavior and biological activity.
【Key words】 Octapeptide cholecystokinin; Liquid-phase method; Pyridinium acetylsulfate;
- 【文献出处】 生物化学杂志 , 编辑部邮箱 ,1991年04期
- 【被引频次】4
- 【下载频次】54