Substituent Effects on Desferrithiocin and Desferrithiocin Analogue Iron-Clearing and Toxicity Profiles

被引:11
作者
Bergeron, Raymond J. [1 ]
Wiegand, Jan [1 ]
Bharti, Neelam [1 ]
McManis, James S. [1 ]
机构
[1] Univ Florida, Dept Med Chem, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
KIDNEY INJURY MOLECULE-1; CHELATION-THERAPY; DESAZADESFERRITHIOCIN ANALOGS; COORDINATION CHEMISTRY; OXIDATIVE DAMAGE; OVERLOAD; DEFERIPRONE; THALASSEMIA; BIOMARKER; ICL670;
D O I
10.1021/jm300509y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Desferrithiocin (DFT, 1) is a very efficient iron chelator when given orally. However, it is severely nephrotoxic. Structure-activity studies with 1 demonstrated that removal of the aromatic nitrogen to provide desazadesferrithiocin (DADFT, 2) and introduction of either a hydroxyl group or a polyether fragment onto the aromatic ring resulted in orally active iron chelators that were much less toxic than 1. The purpose of the current study was to determine if a comparable reduction in renal toxicity could be achieved by performing the same structural manipulations on 1 itself. Accordingly, three DFT analogues were synthesized. The iron-clearing efficiency and ferrokinetics were evaluated in rats and primates; toxicity assessments were carried out in rodents. The resulting DFT ligands demonstrated a reduction in toxicity that was equivalent to that of the DADFT analogues and presented with excellent iron-clearing properties.
引用
收藏
页码:7090 / 7103
页数:14
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