Zhao G, Lin H, Zhu S, Sun H, Chen Y
Department of Chemistry, Nankai University, Tianjin, P.R. China.
Anticancer Drug Des. 1998 Oct;13(7):769-77.
The synthesis of four binuclear platinum complexes of general formula ¿cis-[Pt(NH3)2Cl]2(L)¿ (NO3)2 [L is 4,4'-dipyridyl sulfide (compound I), 4,4'-dipyridyl selenide (compound II), bis(3-methyl-4-pyridyl) sulfide (compound III) or bis(3-methyl-4-pyridyl) selenide (compound IV)] has been achieved. These compounds have been characterized by elemental analysis, IR, 1H-NMR, 13C-NMR and 195Pt-NMR spectroscopy. The above dinuclear platinum complexes have been assayed for antitumor activity in vitro against the cisplatin-sensitive L1210 (the mice leukemia) and cisplatin-insensitive HCT8 (the human coloadenocarcinoma) cell lines. The compounds show IC50 values comparable to or higher than cisplatin against L1210 cell line; however, they have lower IC50 values than cisplatin against the cisplatin-insensitive HCT8 cell line. The complexes containing S exhibit a cytotoxicity against the two cancer cell lines superior to the Se analogues. DNA binding studies indicate the compound I possibly interacts with DNA nonintercalatively. The mode of DNA binding of the dinuclear Pt(II) complexes bridged by 4,4'-dipyridyl selenides or sulfides may be different to that of the aliphatic diaminebridged dinuclear Pt(II) complexes reported previously.
已成功合成了通式为¿顺式-[Pt(NH₃)₂Cl]₂(L)¿ (NO₃)₂的四种双核铂配合物[L为4,4'-二吡啶基硫醚(化合物I)、4,4'-二吡啶基硒醚(化合物II)、双(3-甲基-4-吡啶基)硫醚(化合物III)或双(3-甲基-4-吡啶基)硒醚(化合物IV)]。这些化合物已通过元素分析、红外光谱、¹H-核磁共振、¹³C-核磁共振和¹⁹⁵Pt-核磁共振光谱进行了表征。上述双核铂配合物已针对顺铂敏感的L1210(小鼠白血病)和顺铂不敏感的HCT8(人结肠腺癌)细胞系进行了体外抗肿瘤活性测定。这些化合物对L1210细胞系的IC50值与顺铂相当或更高;然而,它们对顺铂不敏感的HCT8细胞系的IC50值低于顺铂。含硫的配合物对两种癌细胞系的细胞毒性优于含硒类似物。DNA结合研究表明化合物I可能以非嵌入方式与DNA相互作用。由4,4'-二吡啶基硒醚或硫醚桥连的双核Pt(II)配合物的DNA结合模式可能与先前报道的脂肪族二胺桥连的双核Pt(II)配合物不同。