发明名称 TRI- AND TETRA-SUBSTITUTED GUANIDINES AND THEIR USE AS EXCITATORY AMINO ACID ANTAGONISTS
摘要 2076664 9112797 PCTABS00007 Tri- and tetra-substituted guanidines which exhibit a high binding affinity to phencyclidine (PCP) receptors and, more preferably, low affinity to the brain sigma receptors. These guanidine derivatives act as non-competitive inhibitors of glutamate induced responses of the NMDA receptor by acting as blockers for the ion channel of the NMDA receptor-ion channel complex. These compounds thus exert neuroprotective activity and are useful in the therapeutic treatment of neuronal loss in hypoxia, hypoglycemia, brain or spinal cord ischemia, and brain or spinal cord trauma as well as being useful for the treatment of epilepsy, Alzheimer's disease, Amyotrophic Lateral Sclerosis, Parkinson's disease, Huntington's disease, Down's Syndrome, Korsakoff's disease and other neurodegenerative disorders.
申请公布号 CA2076664(A1) 申请公布日期 1991.09.03
申请号 CA19912076664 申请日期 1991.03.04
申请人 STATE OF OREGON, ACTING BY AND THROUGH THE OREGON BOARD OF HIGHER EDUCATION, ACTING FOR AND ON BEHALF OF THE OREGON HEALTH SCIENCES UNIVERSITY, PORTLAND, OREGON, AND THE UNIVERSITY OF OREGON, EUGENE, OREGON 发明人 WEBER, ECKARD;KEANA, JOHN F. W.
分类号 C07D311/08;A61K31/155;A61K31/37;A61P9/04;A61P9/10;A61P25/00;A61P25/08;A61P25/14;A61P25/26;A61P25/28;A61P43/00;B41J2/47;C07C279/02;C07C279/18;C07D311/18;G03G15/16;(IPC1-7):C07C279/00;C07D241/20;A61K31/33;C07D207/34;C07D333/36;C07D239/42;C07D263/48;C07D277/48;C07D307/66;C07D213/75 主分类号 C07D311/08
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