Synthesis and biological evaluation of. some differently substituted 9,10-anthracenediones

被引:14
作者
Cardia, MC
Begala, M
DeLogu, A
Maccioni, E
机构
[1] Dipartimento Farmacochim Tecnol, I-09124 Cagliari, Italy
[2] Dipartimento Sci Chirurg & Trapianti Organo, I-09123 Cagliari, Italy
来源
FARMACO | 2001年 / 56卷 / 08期
关键词
9,10-anthracenediones; amino-acid derivatives; topoisomerase II;
D O I
10.1016/S0014-827X(01)01082-5
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
9,10-Anthracenedione derivatives are known to exhibit a quite potent anticancer activity. It has also been reported that these compounds can be effectively employed in both antibacterial and antitrypanosomal therapy. Anthraquinones also exhibit some undesirable side effects, like cardiotoxicity. So many interactions seem to demonstrate that 9,10-anthracenediones strongly interact with a number of biological sites. In this paper we wish to report on the synthesis and the pharmaceutical activity of some newly synthesised derivatives containing the anthraquinone pharmacophore. (C) 2001 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:549 / 554
页数:6
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