发明公开
EP0574906A2 Piperazine and homopiperazine derivatives, pharmaceutical compositions containing them and process for preparing the same
失效
![Piperazine and homopiperazine derivatives, pharmaceutical compositions containing them and process for preparing the same](/ep/1993/12/22/EP0574906A2/abs.jpg.150x150.jpg)
基本信息:
- 专利标题: Piperazine and homopiperazine derivatives, pharmaceutical compositions containing them and process for preparing the same
- 专利标题(中):哌嗪和Homopiperazinderivate,含有它们的它们的制备方法的药物组合物。
- 申请号:EP93109664.8 申请日:1993-06-17
- 公开(公告)号:EP0574906A2 公开(公告)日:1993-12-22
- 发明人: Zubovics, Zoltán Dr. , Goldschmidt née Horváth, Katalin Dr. , Szilágyi née Farago, Katalin Dr. , Ferenc, Andrási Dr. , Hodula née Szentkuti, Eszter Dr. , Toldy, Lajos Dr. , Sutka, Klára Dr. , Fittler, Zsuzsanna , Sebestyén, Lászlo , Görgényi née Kiss, Katalin Dr. , Sziráki, István Dr. , Gyimesi, Jozsef Dr. , Vitkoczi née Kardos, Valéria
- 申请人: NISSHIN FLOUR MILLING CO., LTD.
- 申请人地址: 19-12, Nihonbashi-koamicho Chuo-ku, Tokyo JP
- 专利权人: NISSHIN FLOUR MILLING CO., LTD.
- 当前专利权人: NISSHIN FLOUR MILLING CO., LTD.
- 当前专利权人地址: 19-12, Nihonbashi-koamicho Chuo-ku, Tokyo JP
- 代理机构: Türk, Gille, Hrabal, Leifert
- 优先权: HU922021 19920617
- 主分类号: C07D239/50
- IPC分类号: C07D239/50 ; C07D403/04 ; C07D475/08 ; A61K31/525 ; A61K31/50 ; A61K31/505 ; C07D239/95 ; C07D237/22
摘要:
The lipid peroxidation inhibiting piperazine and homopiperazine derivatives of the general formula (I) and the pharmaceutically acceptable acid addition salts thereof,
Lip stands for hydrogen ; C 15-20 alkyl ; C 10-20 alkanoyl or C 10-20 alkenoyl ; trityl optionally substituted by halogen ; adamantyl ; 1- or 2-naphthyloxy or oxo-substituted tetrahydronaphthyloxy; or an amine protective group commonly used e.g. in the peptide chemistry;
摘要(中):
Lip stands for hydrogen ; C 15-20 alkyl ; C 10-20 alkanoyl or C 10-20 alkenoyl ; trityl optionally substituted by halogen ; adamantyl ; 1- or 2-naphthyloxy or oxo-substituted tetrahydronaphthyloxy; or an amine protective group commonly used e.g. in the peptide chemistry;
脂质过氧化抑制哌嗪衍生物和通式(I)及其药学上可接受的酸加成盐的高哌嗪,唇代表氢; C15-20烷基; C10-20烷酰基或烯酰基C10-20; 三苯甲基OPTIONALLY substituiertem被卤素; 金刚; 1-或2-萘氧基或氧代tetrahydronaphthyloxy substituiertem; 或胺常用E.G.使用的保护基团 在肽化学; A <1>和A <2>选自unabhängig由单键和C2-3亚烷基被羟基或氧代OPTIONALLY substituiertem被选择; n是1或2; 和Het darstellt的基团,通式(a)的 worin - [R <1>是氨基或1-吡咯烷基; 或4-氯-3-氧代-2,3-二氢-5-哒嗪基的式(b); 或式(c)中的4-氨基-6,7-二甲氧基-2-喹唑啉基; 或式(d)的4,7-二氨基-6-苯基-2-蝶啶基; 或式(e)中的一个2.7二氨基-6-苯基-4-蝶啶基; 或ormula的2,4,7-三氨基-6- pteridinylcarbonyl团(F);
公开/授权文献:
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D239/00 | 杂环化合物,含1,3-二嗪环或氢化1,3-二嗪环 |
--------C07D239/02 | .不与其他环稠合 |
----------C07D239/06 | ..环原子间或环原子与非环原子间有1个双键 |
------------C07D239/28 | ...有杂原子或有以3个键连杂原子、其中最多以1个键连卤素的碳原子,直接连在环碳原子上 |
--------------C07D239/32 | ....1个氧、硫或氮原子 |
----------------C07D239/50 | .....3个氮原子 |