首页> 外国专利> A - amino acid Derivatives arilaminoalquilamida where the carboxyl Group of the amino acid is replaced by a arilamino and amino N of amino acid form a Peptide Bond or pseudo peptidOr, their Preparation and their uses as Pharmaceutical Product utles as inhibitors of lacatepsina K.

A - amino acid Derivatives arilaminoalquilamida where the carboxyl Group of the amino acid is replaced by a arilamino and amino N of amino acid form a Peptide Bond or pseudo peptidOr, their Preparation and their uses as Pharmaceutical Product utles as inhibitors of lacatepsina K.

机译:A-氨基酸衍生物arilaminoalquilamida,其中氨基酸的羧基被arilamino取代,氨基酸的氨基N形成肽键或伪肽Or,它们的制备及其作为药用产品utles用作lacatepsina K抑制剂的用途。

摘要

The Invention provides amino acids arilaminoalquilamidas, where the carboxyl Group of the c-terminal amino acid is replaced by a Substituent arilanoalquilamino,And in which the nitrogen atom of the Amine forms a Peptide Bond or seudopeptido optionally comprises in addition a Linker methylene - heteroatom,Additional or a heteroatom, through which is directly substituted aryl, alkyl alquenilo Lower, Lower, Lower alquinilo, or heterociclilo,Or A physiologically acceptable Salt or Ester and dissociable from the same, including compounds of formula I,Or A physiologically acceptable Salt or Ester thereof.
机译:本发明提供了氨基酸arilaminoalquilamidas,其中c-末端氨基酸的羧基被取代基arilanoalquilamino取代,并且其中的胺的氮原子形成肽键或seudopeptido任选地还包含连接基亚甲基-杂原子,额外的或杂原子,通过其直接取代的芳基,烷基alquenilo低级,低级,低级alquinilo或杂环基,或生理上可接受的盐或酯,并且可与其分解,包括式I的化合物,或生理上可接受的盐或酯其。

著录项

  • 公开/公告号CL2000000334A1

    专利类型

  • 公开/公告日2000-11-23

    原文格式PDF

  • 申请/专利权人 NOVARTIS AG;

    申请/专利号CL2000000334

  • 申请日2000-02-14

  • 分类号C01C211/15;C01C231/02;C01C233/08;C01C237/00;

  • 国家 CL

  • 入库时间 2022-08-22 01:25:53

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