发明授权
- 专利标题: Synthesis of peptide amides by means of a solid phase method using acid-labile anchoring groups
- 专利标题(中): 通过使用酸不稳定锚定基团的固相法合成肽酰胺
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申请号: US178232申请日: 1988-04-06
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公开(公告)号: US4922015A公开(公告)日: 1990-05-01
- 发明人: Gerhard Breipohl , Jochen Knolle , Werner Stuber
- 申请人: Gerhard Breipohl , Jochen Knolle , Werner Stuber
- 申请人地址: DEX Frankfurt am Main
- 专利权人: Hoechst Aktiengesellschaft
- 当前专利权人: Hoechst Aktiengesellschaft
- 当前专利权人地址: DEX Frankfurt am Main
- 优先权: DEX3711866 19870408
- 主分类号: C07C69/675
- IPC分类号: C07C69/675 ; C07C51/00 ; C07C59/125 ; C07C59/68 ; C07C67/00 ; C07C213/00 ; C07C213/02 ; C07C217/58 ; C07C239/00 ; C07C271/08 ; C07C271/34 ; C07K1/04 ; C07K1/08 ; C07K1/113 ; C07K7/16 ; C07K14/575
摘要:
The invention relates to new compounds of the formula ##STR1## in which R.sup.1 denotes (C.sub.1 -C.sub.8)-alkyl or optionally substituted (C.sub.6 -C.sub.14)-aryl, R.sup.2 denotes hydrogen or an amino acid residue which is protected by an amino protective group which can be cleaved off with weak acid or base, R.sup.3 denotes hydrogen or (C.sub.1 -C.sub.4)-alkyl, and Y.sup.1 -Y.sup.9 denote identical or different radicals hydrogen, (C.sub.1 -C.sub.4)-alkyl, (C.sub.1 -C.sub.4)-alkoxy or -O-(CH.sub.2).sub.n -COOH (with n=1 to 6), one of these radicals being -O-(CH.sub.2).sub.n -COOH. A process for the preparation thereof and the synthesis of peptide amides by means of a solid phase method using these new compounds (spacers) are described.
公开/授权文献
- US4312879A Clonidine and lofexidine as antidiarrheal agents 公开/授权日:1982-01-26
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