Substituted 6,11-ethano-6,11-dihydrobenzo[b] quinolizinium salts and
摘要:
替代的6,11-乙烷-6,11-二氢苯并[b]喹啉盐,含有它们的药物组合物,以及利用它们治疗神经退行性疾病或神经毒性损伤的方法,其中替代的6,11-乙烷-6,11-二氢苯并[b]喹啉盐具有以下结构式:##STR1## 其中:R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5、R.sup.6、R.sup.7、X 和 p 如规范中所定义。
Substituted heterocyclylisoquinolinium salts and compositions and method
申请人:Sterling Winthrop Inc.
公开号:US05569655A1
公开(公告)日:1996-10-29
Substitutued heterocyclylisoquinolinium salts, pharmaceutical compositions containing them and methods for the treatment or prevention of neurodegenerative disorders or neurotoxic injuries utilizing them.
取代杂环异喹啉盐,含有它们的药物组合物以及利用它们治疗或预防神经退行性疾病或神经毒性损伤的方法。
Substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts and compositionsand methods of use thereof
申请人:STERLING WINTHROP INC.
公开号:EP0656359A1
公开(公告)日:1995-06-07
Substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts of Formula,
pharmaceutical compositions containing them, and methods for the treatment or prevention of neurodegenerative disorders or neurotoxic injuries utilizing them.
Substituted heterocyclylisoquinolinium salts and compositions and methods of usethereof
申请人:STERLING WINTHROP INC.
公开号:EP0647641A1
公开(公告)日:1995-04-12
Substitutued heterocyclylisoquinolinium salts of Formula
pharmaceutical compositions containing them and methods for the treatment or prevention of neurodegenerative disorders or neurotoxic injuries utilizing them.
Discovery of 6,11-Ethano-12,12-diaryl-6,11-dihydrobenzo[b]quinolizinium Cations, a Novel Class of N-Methyl-D-aspartate Antagonists
作者:Chakrapani Subramanyam、John P. Mallamo、John A. Dority、William G. Earley、Virendra Kumar、Lisa D. Aimone、Brian Ault、Matthew S. Miller、Daniel A. Luttinger、Diane L. DeHaven-Hudkins
DOI:10.1021/jm00001a006
日期:1995.1
6,11-Ethano-12,12-diaryl-6,11-dihydrobenzo[b]quinolizinium cations 8, a novel class of N-methyl-D-aspartate (NMDA) antagonists acting at the phencyclidine site, have been identified. Structure-activity relationship studies around the lead compound 8a led to the identification of 12g (WIN 67870-2), one of the most potent compounds in this series. Compound 12g has a K-i = 1.8 +/- 0.2 nM vs [H-3]TCP binding, has 700-fold selectivity for binding to the open state of the NMDA receptor-ionophore, and was devoid of MK-801- and PCP-like behavioral effects in rats. Compound 12g was neuroprotective in cultured mouse cortical neurons and exhibited antiischemic activity in a rat middle cerebral artery occlusion/reperfusion model of focal ischemia.