作者:T. Birtle、A. J. White、D. P. Woodhouse
DOI:10.1002/jlcr.2580340412
日期:1994.4
The synthesis of salmon calcitonin, a C-terminal amide dotriacontapeptide, labelled with tritium in the leucine residue at position 4 to a specific activity of 100Ci mmole−1 is described. The peptide was assembled using the Fmoc-Polyamide solid-phase synthesis strategy incorporating tritium labelled leucine, in the form of Fmoc-4,5-3H-leucinepentafluorophenylester, at the appropriate stage. The Fmoc-4
描述了鲑鱼降钙素的合成,它是一种 C 端酰胺 dotriacontapeptide,在位置 4 的亮氨酸残基中用氚标记,比活性为 100Ci mmole-1。该肽使用 Fmoc-聚酰胺固相合成策略在适当的阶段以 Fmoc-4,5-3H-亮氨酸五氟苯酯的形式结合氚标记的亮氨酸组装。Fmoc-4,5-3H-亮氨酸五氟苯基酯是通过多阶段合成从 4,5-脱氢亮氨酸制备的。