ACS Appl Mater Interfaces. 2018 Oct 10;10(40):33803-33813. doi: 10.1021/acsami.8b06664. Epub 2018 Sep 28.
Synthetic anion transporters have been recognized as one of the potential therapeutic agents for the treatment of diseases including cystic fibrosis, myotonia, and epilepsy that originate due to the malfunctioning of natural Cl ion transport systems. Recent studies showed that the synthetic Cl ion transporters can also disrupt cellular ion-homeostasis and induce apoptosis in cancer cell lines, leading to a revived attention for synthetic Cl ion transporters. Herein, we report the development of conformationally controlled 1,2-diphenylethylenediamine-based bis(thiourea) derivatives as a new class of selective Cl ion carrier. The strong Cl ion binding properties ( K = 3.87-6.66 mM) of the bis(thiourea) derivatives of diamine-based compounds correlate well with their transmembrane anion transport activities (EC = 2.09-4.15 nM). The transport of Cl ions via Cl/NO antiport mechanism was confirmed for the most active molecule. Perturbation of Cl ion homeostasis by this anion carrier induces cell death by promoting the caspase-mediated intrinsic pathway of apoptosis.
合成阴离子转运体已被认为是治疗囊性纤维化、肌强直和癫痫等疾病的潜在治疗剂之一,这些疾病源于天然 Cl-离子转运系统的功能障碍。最近的研究表明,合成 Cl-离子转运体还可以破坏细胞离子稳态并诱导癌细胞系凋亡,这引起了人们对合成 Cl-离子转运体的重新关注。在此,我们报告了基于手性 1,2-二苯乙烯二胺的双(硫脲)衍生物的开发,作为一类新的选择性 Cl-离子载体。基于二胺的双(硫脲)衍生物的强 Cl-离子结合特性(K = 3.87-6.66 mM)与其跨膜阴离子转运活性(EC = 2.09-4.15 nM)密切相关。最活跃分子的 Cl-离子通过 Cl/NO 反向转运机制的转运得到了证实。这种阴离子载体通过促进半胱天冬酶介导的细胞凋亡内在途径破坏 Cl 离子稳态,从而诱导细胞死亡。