CAS: 61315-61-5; Boc-D-Arg(Tos)-Oh

该化合物是D-arginine受保护的衍生物,其特点是基-丁基碳基(Boc)和Tosyl(Tos)分别保护氨基和瓜尼地诺功能的组群.该化合物广泛用于peptide合成,特别是采用正方位保护战略引入D-arginine残留物.Boc组确保在基本条件下保持稳定,而Tos组则在组合反应中保障瓜尼丁的团结.其高纯度和定义明确的保护计划促进了高效固相和溶解相聚.该产品在改良的peptides合成中特别有用,因为在此合成中,立体化学完整性和选择性除物至关重要.适合需要精确控制序列的研究和工业应用.

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1119-34-2 114622-81-0 1159-15-5

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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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