Egan Timothy J, Koch Klaus R, Swan Paul L, Clarkson Cailean, Van Schalkwyk Donelly A, Smith Peter J
Department of Chemistry, University of Cape Town, Private Bag, Rondebosch 7701, South Africa.
J Med Chem. 2004 May 20;47(11):2926-34. doi: 10.1021/jm031132g.
We have synthesized a series of novel 2,2'-bipyridyl and 1,10-phenanthroline benzoylthiourea complexes of platinum(II) with various substituents on the bipyridyl and phenanthroline ligands. All of these square-planar mixed-ligand cationic complexes were found to form moderately strong complexes with ferriprotoporphyrin IX in 40% aqueous DMSO (log K ranging from 4.81 to 6.24). The complexes also all inhibit beta-hematin (synthetic hemozoin or malaria pigment) formation in acetate solution. Four of the compounds were found to exhibit in vitro antimalarial activity, with (N-benzoyl-N',N'-di(2-hydroxyethyl)thioureato)(4,4'-di-tert-butyl-2,2'-bipyridyl)platinum(II) chloride being particularly active. These active complexes exhibited equally strong activity against both the D10 chloroquine sensitive and K1 chloroquine resistant strains of malaria parasite. Cytotoxicity testing of the four most active compounds shows that they exhibit selective activity against malaria parasites with selectivity indices greater than 85. These compounds represent a new family of potential antimalarials.
我们合成了一系列新型的铂(II)的2,2'-联吡啶和1,10-菲咯啉苯甲酰硫脲配合物,其中联吡啶和菲咯啉配体上带有各种取代基。发现所有这些平面四方混合配体阳离子配合物在40%的二甲基亚砜水溶液中与高铁原卟啉IX形成中等强度的配合物(log K范围为4.81至6.24)。这些配合物还均能抑制醋酸盐溶液中β-血红素(合成疟原虫色素或疟色素)的形成。发现其中四种化合物具有体外抗疟活性,其中(N-苯甲酰基-N',N'-二(2-羟乙基)硫脲基)(4,4'-二叔丁基-2,2'-联吡啶)氯化铂(II)特别活跃。这些活性配合物对疟原虫的D10氯喹敏感株和K1氯喹耐药株均表现出同样强的活性。对四种活性最高的化合物进行细胞毒性测试表明,它们对疟原虫表现出选择性活性,选择性指数大于85。这些化合物代表了一类新 的潜在抗疟药物。