期刊
INORGANICA CHIMICA ACTA
卷 451, 期 -, 页码 31-40出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2016.06.036
关键词
Palladium(II) dithiocarbamates; Anticancer drugs; DNA-binding and DNA-denaturing
资金
- Higher Education Commission of Pakistan
Although it is well known that cisplatin and its analogues are effective anticancer agents, but their clinical use is restricted by some serious side effects. Palladium complexes are emerged as alternative metalloanticancer drugs merited by their structural similarity to platinum(II) complexes, more labile nature, minimal chemoresistance and often water solubility. However, due to exceptional high reactivity of palladium complexes than their platinum counterparts, they are not only obstructed by the sulfur containing molecules to reach their pharmacological targets but also significantly enhance their affinity to convert into inactive trans isomers. This hitch can be overcome by the use of appropriate ligands that can have the potential to turn down the negative lability to positive inertness. This review provides a summary of the anticancer potential, DNA-binding and DNA-denaturing aptitude of various palladium (II) dithiocarbamates in which the presence of the dithiocarbamate moiety significantly improves the anticancer action and, at the same time, reduces the possibility of any damaging side effects. (C) 2016 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据