Department of Medical Biology, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
Department of Chemistry, Engineering Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
J Biochem Mol Toxicol. 2019 Oct;33(10):e22383. doi: 10.1002/jbt.22383. Epub 2019 Aug 8.
Eighteen of the iron(III) and nickel(II) complexes with tetradentate thiosemicarbazidato ligands were synthesized and described, by analytical and spectroscopic methods. Two complexes as an example to the iron and nickel centered ones were crystallographically analyzed to confirm the molecular structures. Cytotoxic effects of the complexes on K562 chronic myeloid leukemia cells were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. For comparison, human umbilical vein endothelial cells (HUVECs) was used as a noncancerous cell line. While four of the iron(III) complexes exhibited the antileukemic effect with 50% inhibition of cell growth (IC ) values in the 3.4 to 6.9 μg/mL range on K562 cell line, the nickel(II) complexes showed no significant effect on both cell lines. The complexes Fe4, Fe5, and Fe6, bearing 4-methoxy substituent exhibited relatively high antiproliferative activity on both cell lines. Complex Fe3 with 3-methoxy and S-allyl groups exhibited a selectivity between K562 and HUVEC cells by IC values of 6.9 and >10 μg/mL, respectively. Lipophilicity, a key parameter for bioavailability and oral administration, was found in the range of -0.3 and +1.3 that desired for drug active ingredients. The results were discussed in the context of a structure-activity relationship.
十八个铁(III)和镍(II)配合物与四齿硫代半卡巴腙配体通过分析和光谱方法合成并描述。以铁和镍为中心的两个配合物为例进行了晶体结构分析,以确认分子结构。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐测定法测定了配合物对 K562 慢性髓系白血病细胞的细胞毒性作用。为了比较,用人脐静脉内皮细胞(HUVEC)作为非癌细胞系。虽然四个铁(III)配合物对 K562 细胞系具有抗白血病作用,细胞生长抑制 50%时的半数抑制浓度 (IC ) 值在 3.4 至 6.9μg/mL 范围内,但镍(II)配合物对两种细胞系均无明显作用。具有 4-甲氧基取代基的配合物 Fe4、Fe5 和 Fe6 对两种细胞系均表现出相对较高的增殖抑制活性。具有 3-甲氧基和 S-烯丙基的配合物 Fe3 对 K562 和 HUVEC 细胞的 IC 值分别为 6.9 和>10μg/mL,具有选择性。亲脂性是生物利用度和口服给药的关键参数,其范围在-0.3 至+1.3,这是药物有效成分所需的范围。结果在结构-活性关系的背景下进行了讨论。