基本信息:
- 专利标题: N-아실-N'-벤질-알킬렌디아미노 유도체
- 专利标题(英):N-acyl-n'-benzyl-alkylendiamino derivatives
- 专利标题(中):N-乙酰基-N'-苄基-L-鸟氨酸衍生物
- 申请号:KR1020067010037 申请日:2004-11-12
- 公开(公告)号:KR1020060111523A 公开(公告)日:2006-10-27
- 发明人: 탈레르플로리안 , 사비도다비드시벨레마리아 , 파라벨리라우라 , 가글리아르디스테파니아 , 콜롬보엘레나 , 살바티파트리시아
- 申请人: 뉴론 파마슈티칼즈 에스. 피. 에이.
- 申请人地址: 이탈리아 아이-***** 밀란 브레소 비아 엘. 아리오스토 **
- 专利权人: 뉴론 파마슈티칼즈 에스. 피. 에이.
- 当前专利权人: 뉴론 파마슈티칼즈 에스. 피. 에이.
- 当前专利权人地址: 이탈리아 아이-***** 밀란 브레소 비아 엘. 아리오스토 **
- 代理人: 리앤목특허법인
- 优先权: EP030270441 2003-11-24
- 国际申请: PCT/EP2004/012834 2004-11-12
- 国际公布: WO2005054189 2005-06-16
- 主分类号: C07C233/36
- IPC分类号: C07C233/36 ; C07D207/27 ; C07D207/267
摘要:
This invention is related to compounds and use of N-Acyl-N'-benzyl-alkylendiamino derivatives of the following general formula (I), wherein A is a straight or branched C 2-C8 alkyl chain; X is a methylene, oxygen, sulphur or a NR7 group; R1is a straight or branched C1-C8 alkyl or C3-C8 alkenylene or C3-C8alkynylene chain, optionally substituted with CF3, phenyl, phenoxy or naphthyl, the aromatic rings optionally substituted by one or more C1-C4 alkyl, halogens, trifluoromethyl, hydroxy or C1-C4 alkoxy groups; R2, R3 are independently hydrogen, a C1 -C3 alkyl chain, halogen, trifluoromethyl, hydroxy or C1 -C4 alkoxy groups; R4, R5 are independently hydrogen or C1-C6alkyl; R6 is a hydrogen or a straight or branched C1-C8 alkyl or linked to R 5 can form a five to seven membered lactam; R7is hydrogen or C1-C6 alkyl; and the pharmaceutically acceptable salts thereof that are active as sodium and/or calcium channel modulators and therefore useful in preventing, alleviating and curing a wide range of pathologies, including, but not limited to, neurological, psychiatric, cardiovascular, inflammatory, ophthalmic, urologic, metabolic and gastrointestinal diseases, where the above mechanisms have been described as playing a pathological role.
摘要(中):
本发明涉及以下通式(I)的N-酰基-N'-苄基 - 烷基二氨基衍生物的化合物和用途,其中A是直链或支链C 2 -C 8烷基链; X是亚甲基,氧,硫或NR 7基团; R1是任选被CF 3,苯基,苯氧基或萘基取代的直链或支链C 1 -C 8烷基或C 3 -C 8亚链烯基或C 3 -C 8亚炔基链,芳环任选被一个或多个C 1 -C 4烷基,卤素,三氟甲基,羟基 或C 1 -C 4烷氧基; R2,R3独立地是氢,C1-C3烷基链,卤素,三氟甲基,羟基或C1-C4烷氧基; R4,R5独立地是氢或C1-C6烷基; R 6是氢或直链或支链C 1 -C 8烷基或与R 5连接可以形成5至7元的内酰胺; R7是氢或C1-C6烷基; 其作为钠和/或钙通道调节剂具有活性的药学上可接受的盐,因此可用于预防,减轻和治愈广泛范围的病症,包括但不限于神经,精神,心血管,炎症,眼科,泌尿系统 ,代谢和胃肠道疾病,其中上述机制被描述为发挥病理作用。
信息查询:
EspacenetIPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07C | 无环或碳环化合物 |
------C07C233/00 | 羧酸酰胺 |
--------C07C233/01 | .羧酰胺基的碳原子连接在氢原子或非环碳原子上 |
----------C07C233/02 | ..羧酰胺基的氮原子连接在氢原子或未取代烃基碳原子上 |
------------C07C233/35 | ...有由非环碳原子连接在羧酰胺基的氮原子上的取代烃基 |
--------------C07C233/36 | ....羧酰胺基的碳原子连接在氢原子或无环饱和碳架的碳原子上 |