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.