Investigation into the structure-activity relationship of novel concentration dependent, dual action T-type calcium channel agonists/antagonists

被引:32
作者
McCalmont, WF [1 ]
Patterson, JR
Lindenmuth, MA
Heady, TN
Haverstick, DM
Gray, LS
MacDonald, TL
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
[2] Univ Virginia, Dept Pathol, Charlottesville, VA 22904 USA
关键词
T-type calcium channels; concentration dependent dual antagonist/agonist; cancer;
D O I
10.1016/j.bmc.2005.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes the synthesis and biological evaluation of a series of straight chain analogs of a compound (1) that was previously synthesized in our research program. These compounds, which are T-type calcium channel antagonists, exhibits potent anti-proliferative activity against a variety of cancer cells. A structure-activity relationship of these analogs against a variety of cancer cells has provided insight into a logical pharmacophore for this series of compounds. Furthermore, this series of compounds has presented itself as a set of novel, concentration dependent, dual action agonists/antagonists for the T-type calcium channel. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3821 / 3839
页数:19
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