Dehkordi Lotfollah S, Liu Zu D, Hider Robert C
School of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.
Eur J Med Chem. 2008 May;43(5):1035-47. doi: 10.1016/j.ejmech.2007.07.011. Epub 2007 Aug 2.
3-Hydroxypyridin-4-ones selectively bind iron under biological conditions and one such compound has found application in the treatment of thalassaemia-linked iron overload. Related molecules have also been demonstrated to possess an antimalarial effect at levels which are non-toxic to mammalian cells. In an attempt to improve the efficiency of such molecules we have investigated the effect of introducing basic nitrogen centres into 3-hydroxypyridin-4-ones in an attempt to achieve targeting to lysosomes and other intracellular acidic vacuoles. Several of the compounds reported in this communication possess enhanced antimalarial activity over that of the simple hydroxypyridinone class.
3-羟基吡啶-4-酮在生物条件下能选择性地结合铁,并且有一种这样的化合物已被应用于治疗与地中海贫血相关的铁过载。相关分子也已被证明在对哺乳动物细胞无毒的水平上具有抗疟作用。为了提高这类分子的效率,我们研究了在3-羟基吡啶-4-酮中引入碱性氮中心的效果,以期实现靶向溶酶体和其他细胞内酸性液泡。本通讯报道的几种化合物比简单的羟基吡啶酮类具有更强的抗疟活性。