Ong Yih Ching, Blair Victoria L, Kedzierski Lukasz, Tuck Kellie L, Andrews Philip C
School of Chemistry, Monash University, Clayton, Melbourne, VIC 3800, Australia.
Dalton Trans. 2015 Nov 7;44(41):18215-26. doi: 10.1039/c5dt03335g. Epub 2015 Oct 1.
A series of 29 tris-tolyl bismuth(v) di-carboxylato complexes of composition [Bi(Tol)3(O2CR)2] involving either ortho, meta or para substituted tolyl ligands have been synthesized and characterised. Of these 15 were assessed for their toxicity towards Leishmania promastigotes and human fibroblast cells, with ten then being subsequently assessed against parasite amastigotes. The carboxylate ligands are drawn from a series of substituted and biologically relevant benzoic acids which allow a comparison with earlier studies on [BiPh3(O2CR)2] and analogous Sb(v) [SbAr3(O2CR)2] (Ar = Ph and Tol) complexes. Twelve complexes have been structurally characterized by single crystal X-ray diffraction and shown to adopt a typical trigonal bipyramidal geometry in which the three tolyl ligands occupy the equatorial plane. NMR studies on two illustrative examples indicate that the complexes are stable in D2O and DMSO but only have a half-life of 1.2 hours in culture medium, with glucose being a contributing factor in decomposition and reduction to Bi(Tol)3. Despite their short lifetime many complexes show significant toxicity towards promastigotes at low concentration (<6 μM) and at that concentration provide for good selectivity indices (parasite vs. mammalian cells), for example 114 for [Bi(o-Tol)3(O2CC6H3(2-OH,5-C6H3(2,4-F2)))2] and 838 for [Bi(m-Tol)3(O2CC6H4(2-OAc))2]. Best activity and selectivity is observed with complexes containing o- and m-tolyl ligands, and it appears the primary influence on fibroblast toxicity is the Ar ligand while the carboxylate influences promastigote toxicity. The complexes are less effective in vitro against the parasite amastigotes, where longer incubation times and harsher chemical and biological environments are encountered in the assay. Nevertheless, there were some statistically relevant differences at 1 μM against the positive controls with the best performing complexes being [Bi(o-Tol)3(O2CC6H4(2-EtO))2] and [Bi(m-Tol)3(O2CC6H4(2-OAc))2].
合成并表征了一系列29种组成为[Bi(Tol)3(O2CR)2]的三(甲苯基)铋(Ⅴ)二羧酸酯配合物,其中甲苯基配体为邻位、间位或对位取代。对其中15种配合物对利什曼原虫前鞭毛体和人成纤维细胞的毒性进行了评估,随后对其中10种配合物针对寄生虫无鞭毛体进行了评估。羧酸酯配体取自一系列取代的且具有生物学相关性的苯甲酸,这使得可以与早期关于[BiPh3(O2CR)2]和类似的锑(Ⅴ)[SbAr3(O2CR)2](Ar = Ph和Tol)配合物的研究进行比较。通过单晶X射线衍射对12种配合物进行了结构表征,结果表明它们呈现典型的三角双锥几何构型,其中三个甲苯基配体占据赤道平面。对两个示例的核磁共振研究表明,这些配合物在D2O和DMSO中稳定,但在培养基中的半衰期仅为1.2小时,葡萄糖是分解并还原为Bi(Tol)3的一个促成因素。尽管它们的寿命较短,但许多配合物在低浓度(<6 μM)下对前鞭毛体显示出显著毒性,并且在该浓度下具有良好的选择性指数(寄生虫与哺乳动物细胞),例如[Bi(o-Tol)3(O2CC6H3(2-OH,5-C6H3(2,4-F2)))2]的选择性指数为114,[Bi(m-Tol)3(O2CC6H4(2-OAc))2]的选择性指数为838。含有邻位和间位甲苯基配体的配合物表现出最佳的活性和选择性,似乎对成纤维细胞毒性的主要影响因素是芳基配体,而羧酸酯影响前鞭毛体毒性。这些配合物在体外对寄生虫无鞭毛体的效果较差,在该检测中会遇到更长的孵育时间以及更苛刻的化学和生物环境。然而,在1 μM时与阳性对照相比存在一些统计学上相关的差异,表现最佳的配合物是[Bi(o-Tol)3(O2CC6H4(2-EtO))2]和[Bi(m-Tol)3(O2CC6H4(2-OAc))2]。