CAS: 57096-11-4; N-Boc-N'-[(2-Chlorobenzyloxy)Carbonyl]-D-Lysine

该化合物是属于氨基酸类的化学化合物,特别是赖氨酸的衍生物,它具有三丁基氧碳基(Boc)保护组,通常用于浸泡物合成,以保护氨基组不受不受欢迎的反应.该组还包含一个2-氯苯基(Cbz)组,作为碳箱基组的保护组,在合成过程中加强它的稳定性和再活性.氯原子在苯基环的2位置上的存在,会影响化合物的再活性和溶性.这种化合物通常用于有机合成,特别是在制作浸泡剂和其他复杂分子时.其结构允许选择性反应,使其在药用化学和药物开发中具有价值.与许多化学物质一样,适当的处理和安全防范措施对于其成分的潜在危害至关重要.

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    专利信息


    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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    合成参考文献


    参考文献:10.1007/978-1-4939-8582-1_4
    摘要:Manicardi A, Gambari R, de Cola L, Corradini R. Preparation of Anti-miR PNAs for Drug Development and Nanomedicine. Methods Mol Biol. 2018;1811():49–63. doi: 10.1007/978-1-4939-8582-1_4.
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