Gold compounds as aquaporin inhibitors: new opportunities for therapy and imaging

被引:28
作者
de Almeida, Andreia [1 ]
Soveral, Graca [2 ]
Casini, Angela [1 ]
机构
[1] Univ Groningen, Dept Pharmacokinet Toxicol & Targeting, Res Inst Pharm, NL-9713 AV Groningen, Netherlands
[2] Univ Lisbon, Fac Farm, Inst Invest Medicamento iMed ULisboa, P-1649003 Lisbon, Portugal
关键词
GLYCEROL PERMEABILITY; WATER PERMEABILITY; CELL-MIGRATION; CHANNEL; SELECTIVITY; EXPRESSION; AGENTS; AQUAGLYCEROPORIN; AQP9; GENE;
D O I
10.1039/c4md00265b
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
In recent years, gold-based compounds have been proved to hold promise in chemical biology being able to selectively inhibit proteins activities in cells and, therefore, to be exploited as either therapeutic agents or as chemical tools to detect protein/enzyme functions in living systems. In this area, we have recently described the properties of gold coordination complexes as potent and selective inhibitors of human aquaporins, protein channels involved in the transport of water and glycerol across biomembranes. Thus, we provide here an overview of the importance of aquaporins in various diseases and a detailed description of the state-of-the art progresses in the discovery of new inhibitors, including gold(III) complexes, and a description of their possible applications. Overall, the potential of coordination chemistry in providing compounds to modulate the activity of "elusive" drug targets, such as the aquaporins, will be discussed.
引用
收藏
页码:1444 / 1453
页数:10
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