发明名称 |
Quinoxalinediones, preparation and pharmaceutical compositions thereof |
摘要 |
he compounds of formula (I) and the pharmaceutically acceptable salts thereof wherein: R is an optionally substituted, optionally benzo-fused 5-membered ring heteroaryl group containing 3 or 4 nitrogen heteroatoms which is linked to the quinoxalinedione ring by a ring carbon or nitrogen atom or R is an optionally substituted, optionally benzo-fused 6-membered ring heteroaryl group containing from 1 to 3 nitrogen heteroatoms which is linked to the quinoxalinedione ring by a ring carbon atom; R1 and R2 are independently H, fluoro, chloro, bromo, alkyl or haloalkyl; R3 and R4 are independently H or alkyl or together are alkylene and p is 0, 1 or 2 are claimed. A pharmaceutical composition containing a compound of formula I useful as a NMDA receptor antagonist for treating acute neurodegenerative and chronic neurological disorders is also claimed.
|
申请公布号 |
NZ331060(A) |
申请公布日期 |
2000.01.28 |
申请号 |
NZ19970331060 |
申请日期 |
1997.02.27 |
申请人 |
PFIZER RESEARCH & DEVELOPMENT COMPANY NV /SA |
发明人 |
BULL, DAVID JOHN;CARR, CHRISTOPHER LEE;FRAY, MICHAEL JONATHAN;GAUTIER, ELISABETH COLETTE LOUISE;MOWBRAY, CHARLES ERIC;STOBIE, ALAN |
分类号 |
A61K31/495;A61K31/498;A61K31/505;A61K31/506;A61K31/535;A61K31/5377;A61P25/00;A61P25/28;A61P43/00;C07D241/44;C07D401/04;C07D401/14;C07D403/04;C07D403/14;C07D409/14;C07D413/14;C07D417/14;C07D521/00;(IPC1-7):C07D241/44 |
主分类号 |
A61K31/495 |
代理机构 |
|
代理人 |
|
主权项 |
|
地址 |
|