Synthesis and structure-activity relationship of substituted 1,2,3,4-tetrahydroisoquinolines as N-type calcium channel blockers
作者:Po-wai Yuen、Robert M. Schelkun、Balazs Szoke、Katalin Tarczy-Hornoch
DOI:10.1016/s0960-894x(98)00440-5
日期:1998.9
Voltage Activated Calcium Channel (VACC) blockers have been demonstrated to have utility in the treatment of pain and stroke. A series of aminomethyl substituted isoquinolinol derivatives with potent functional activity for N-type VACC's have been identified. Their synthesis and preliminary pharmacology are discussed herein. (C) 1998 Elsevier Science Ltd. All rights reserved.
Substituted quinolines and isoquinolines as calcium channel blockers,
申请人:Warner-Lambert Company
公开号:US05767129A1
公开(公告)日:1998-06-16
The present invention relates to novel substituted quinolines and isoquinolines and derivatives thereof useful in the treatment of neurological disorders. Methods of preparing the compounds, intermediates useful in the preparation and pharmaceutical compositions containing the compounds are also included. The compounds are useful in treating pain, cerebral ischemia, and other cerebrovascular disorders.