TRICYCLIC QUINOXALINES AS LIGANDS FOR THE STRYCHNINE-INSENSITIVE GLYCINE SITE

被引:8
作者
JACKSON, PF
DAVENPORT, TW
RESCH, JF
LEHR, GS
PULLAN, LM
机构
[1] Biomedical Research Department, ICI Pharmaceuticals Group, Wilmington
关键词
D O I
10.1016/S0960-894X(01)81062-3
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The synthesis of a series of tricyclic quinoxalines is described. These compounds exhibit good affinity for both the strychnine-insensitive glycine site of the NMDA receptor and the AMPA receptor.
引用
收藏
页码:751 / 756
页数:6
相关论文
共 16 条
[1]   GEOMETRY OPTIMIZATION IN CARTESIAN COORDINATES - THE END OF THE Z-MATRIX [J].
BAKER, J ;
HEHRE, WJ .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1991, 12 (05) :606-610
[2]  
CARPENTER JE, 1990, SPARTAN SYSTEM
[3]   QUINOXALINES AND RELATED COMPOUNDS .8. REACTIONS OF QUINOXALINE-2(1H)-ONES AND QUINOXALINE-2,3(1H,4H)-DIONES WITH HYDRAZINE [J].
CHEESEMAN, GW ;
RAFIQ, M .
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1971, (03) :452-+
[4]  
DAVEY DD, 1990, Patent No. 400583
[5]   GLYCINE POTENTIATES THE NMDA RESPONSE IN CULTURED MOUSE-BRAIN NEURONS [J].
JOHNSON, JW ;
ASCHER, P .
NATURE, 1987, 325 (6104) :529-531
[6]   ANTAGONISM OF NON-NMDA RECEPTORS AUGMENTS THE NEUROPROTECTIVE EFFECT OF NMDA RECEPTOR BLOCKADE IN CORTICAL CULTURES SUBJECTED TO PROLONGED DEPRIVATION OF OXYGEN AND GLUCOSE [J].
KAKU, DA ;
GOLDBERG, MP ;
CHOI, DW .
BRAIN RESEARCH, 1991, 554 (1-2) :344-347
[8]   KYNURENIC ACID-DERIVATIVES - STRUCTURE-ACTIVITY-RELATIONSHIPS FOR EXCITATORY AMINO-ACID ANTAGONISM AND IDENTIFICATION OF POTENT AND SELECTIVE ANTAGONISTS AT THE GLYCINE SITE ON THE N-METHYL-D-ASPARTATE RECEPTOR [J].
LEESON, PD ;
BAKER, R ;
CARLING, RW ;
CURTIS, NR ;
MOORE, KW ;
WILLIAMS, BJ ;
FOSTER, AC ;
DONALD, AE ;
KEMP, JA ;
MARSHALL, GR .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (04) :1243-1252
[9]  
LODGE D, 1991, TRENDS PHARM SCI
[10]  
LOFTUS P, 1986, CHEM DESIGN AUTOMA