Bergeron Raymond J, Singh Shailendra, Bharti Neelam, Jiang Yi
Department of Medicinal Chemistry, University of Florida, Box 100485 JHMHC, Gainesville, FL, 32610-0485, USA.
Synthesis (Stuttg). 2010;2010(21):3631-3636. doi: 10.1055/s-0030-1258245.
Iron chelators have been shown to control the growth of cancer cells in culture by sequestering exogenous iron in the media. Thus, the ligands prevent cellular access to the metal. However, because transferrin provides iron to tumor cells in animals, chelators have not been effective antitumor agents. Polyamine chelator conjugates in which the polyamine vectored ligands into cells were far more active than the free chelators themselves. However, the free ligands were not released from the vector once in the cell. The current study focuses on the synthesis and preliminary evaluation of a polyamine chelator conjugate capable of releasing the free ligand intracellularly via a nonspecific esterase.
铁螯合剂已被证明可通过螯合培养基中的外源性铁来控制培养的癌细胞的生长。因此,这些配体可防止细胞获取金属。然而,由于转铁蛋白为动物体内的肿瘤细胞提供铁,螯合剂一直不是有效的抗肿瘤药物。其中多胺将配体导向细胞内的多胺螯合剂缀合物比游离螯合剂本身的活性高得多。然而,游离配体一旦进入细胞就不会从载体上释放出来。当前的研究集中在一种能够通过非特异性酯酶在细胞内释放游离配体的多胺螯合剂缀合物的合成及初步评估上。