CAS: 69541-68-0; Boc-D-His(Tos)-Oh

该化合物是一种乳性氨基酸衍生物,具有乙氧-丁氧碳基(Boc)保护性组和三氟保护的亚丁二甲基的副链.该化合物因其在保持立体化学完整性的同时能够引入二硝基苯甲醚功能,在peptide合成和药用化学中特别有用.Boc组确保在温酸条件下有选择地进行保护,促进进一步的修改.Tosyl组在合成过程中增强稳定性.其结构特征使它成为设计生物活性分子的多功能中间体,包括酶抑制剂和感应器.高纯度和定义精良度的气度确保研究应用中的再生性.适合用于固基聚苯乙烯合成和复杂热循环系统的建筑块.

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    专利号:US-2004110228-A1
    优先权日:2002-04-01
    标 题:Combinatorial organic synthesis of unique biologically active compounds
    发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
    摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

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