首页> 外国专利> METHOD FOR PRODUCING CYCLIZED PEPTIDE HAVING INTRAMOLECULAR S-S BOND

METHOD FOR PRODUCING CYCLIZED PEPTIDE HAVING INTRAMOLECULAR S-S BOND

机译:产生具有分子内S-S键的环化肽的制备方法

摘要

Cyclized peptides having a crosslinked structure by one or more intramolecular S—S bonds may be prepared by:;(1-A) as to a completely protected linear peptide having two or more SH groups as functional groups on the peptide, removing protecting groups of all functional groups other than the protected SH groups in the peptide,(1-B) protecting all SH groups of the linear peptide having two or more SH groups as the functional groups on the peptide by forming a temporary S—S bond,and(2) subjecting the peptide obtained by step (1-A) and step (1-B) to a folding step under oxidation and reduction conditions to obtain the cyclized peptide by re-forming an S—S bond in the peptide molecule.
机译:通过一个或多个分子内S-S键合的具有交联结构的环化肽可以通过:;(1-a)至肽的完全受保护的线性肽,作为肽上的官能团,除去保护基团 除了肽中的受保护SH基团以外的所有官能团,通过形成临时S-S键,保护具有两个或更多个SH基团的线性肽的所有SH组作为肽上的官能团。( 2)使步骤(1-A)和步骤(1-B)获得的肽在氧化下折叠步骤和还原条件,以通过在肽分子中重新形成S-S键来获得环化肽。

著录项

  • 公开/公告号US2021277063A1

    专利类型

  • 公开/公告日2021-09-09

    原文格式PDF

  • 申请/专利权人 AJINOMOTO CO. INC.;

    申请/专利号US202117319346

  • 申请日2021-05-13

  • 分类号C07K7/64;C07K1/107;C07K1/06;

  • 国家 US

  • 入库时间 2024-06-14 22:02:34

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