Balas V I, Verginadis I I, Geromichalos G D, Kourkoumelis N, Male L, Hursthouse M B, Repana K H, Yiannaki E, Charalabopoulos K, Bakas T, Hadjikakou S K
Section of Inorganic and Analytical Chemistry, Department of Chemistry, University of Ioannina, 45110 Ioannina, Greece.
Eur J Med Chem. 2011 Jul;46(7):2835-44. doi: 10.1016/j.ejmech.2011.04.005. Epub 2011 Apr 8.
The reaction between 2-thiobarbituric acid (H(2)TBA), which was treated with an equimolar amount of potassium hydroxide, in a water with triphenytin chloride in methanol, results in the formation of the {[Ph(3)Sn(O-HTBA)]}(n) (1) complex. Crystals of the hydrated 1 with formula {[Ph(3)Sn(O-HTBA)]·0.7(H(2)O)}(n) were growth from methanol/acetonitrile solution, of the white precipitation, filtered off, from the reaction. The crystal structure of complex 1 has been determined by X-ray diffraction at 120 K. Complex 1 is polymeric. The geometry around the tin(IV) ions is trigonal bi-pyramidal with coordination to three C atoms from phenyl groups and one O atom from a de-protonated HTBA ligand. Complex 1 and the already known [(n-Bu)(3)Sn(O-HTBA)·H(2)O] (2) were evaluated for their in vitro cytotoxic activity (cell viability) against human cancer cell lines: HeLa (cervical), OAW-42 (ovarian), MCF-7 (breast, ER positive), MDA-MB-231 (breast, ER negative), A549 (lung), Caki-1 (renal) and additionally, the normal human lung cell line MRC-5 (normal human fetal lung fibroblast cells) and normal immortalized human mammary gland epithelial cell line MTSV17 with a Trypan Blue assay. Moreover complex 1 was evaluated for its in vitro cell growth proliferation activity against leiomyosarcoma cells (LMS), MCF-7 and MRC-5 cells with a Thiazolyl Blue Tetrazolium Bromide (MTT) assay. The type of cell death caused by complexes 1 and 2 was also evaluated by use of flow cytometry assay. The results showed that these compounds mediate a strong cytotoxic response to normal and cancer cell lines tested through apoptosis and induce cell cycle arrest in S phase of the cell cycle, suggesting DNA intercalation (direct or indirect) with the complexes. Finally, the influence of these complexes 1 and 2 upon the catalytic peroxidation of linoleic acid to hydroperoxylinoleic acid by the enzyme lipoxygenase (LOX) was kinetically and theoretically studied.
将等摩尔量的氢氧化钾处理过的2-硫代巴比妥酸(H₂TBA)与甲醇中的三苯基氯化锡在水中反应,生成{[Ph₃Sn(O - HTBA)]}ₙ(1)配合物。从甲醇/乙腈溶液中培养出化学式为{[Ph₃Sn(O - HTBA)]·0.7(H₂O)}ₙ的水合1的晶体,该晶体来自反应产生的白色沉淀,经过过滤得到。配合物1的晶体结构已通过在120 K下的X射线衍射确定。配合物1是聚合物。锡(IV)离子周围的几何构型为三角双锥,与来自苯基的三个C原子和来自去质子化的HTBA配体的一个O原子配位。通过台盼蓝测定法,对配合物1和已知的[(n - Bu)₃Sn(O - HTBA)·H₂O](2)针对人癌细胞系:HeLa(宫颈癌)、OAW - 42(卵巢癌)、MCF - 7(乳腺癌,雌激素受体阳性)、MDA - MB - 231(乳腺癌,雌激素受体阴性)、A549(肺癌)、Caki - 1(肾癌),以及另外的正常人肺细胞系MRC - 5(正常人胎儿肺成纤维细胞)和正常永生化人乳腺上皮细胞系MTSV17的体外细胞毒性活性(细胞活力)进行了评估。此外,通过噻唑蓝四唑溴盐(MTT)测定法,对配合物1针对平滑肌肉瘤细胞(LMS)、MCF - 7和MRC - 5细胞的体外细胞生长增殖活性进行了评估。还通过流式细胞术测定法评估了配合物1和2引起的细胞死亡类型。结果表明,这些化合物通过凋亡介导对所测试的正常和癌细胞系的强烈细胞毒性反应,并诱导细胞周期停滞在细胞周期的S期,表明配合物与DNA发生了插层作用(直接或间接)。最后,从动力学和理论上研究了这些配合物1和2对脂氧合酶(LOX)催化亚油酸过氧化生成氢过氧化亚油酸的影响。