Quiroga A G, Pérez J M, López-Solera I, Montero E I, Masaguer J R, Alonso C, Navarro-Ranninger C
Departamento de Química Inorgánica, Facultad de Ciencias, Universidad Autónoma de Madrid, Spain.
J Inorg Biochem. 1998 Mar;69(4):275-81. doi: 10.1016/s0162-0134(98)00003-8.
Two novel dimeric chloro-bridged complexes [Pd (p-is. TSCN) (mu-Cl)]2, 2, and [Pt (p-is. TSCN)(mu-Cl)]2, 3, where p-is. TSCN = p-isopropylbenzaldehyde thiosemicarbazone, 1, have been synthesized and characterized by IR and NMR spectroscopy. The in vitro antitumor activity shown by both compounds against several human and murine cell lines sensitive and resistant to the clinically-used drug cisplatin (cis-DDP) suggests that compounds 2 and 3 may be endowed with important anticancer properties. Thus, compounds 2 and 3 not only show IC50 values in the microM range as cis-DDP but also display cytotoxic activity in tumor cell lines resistant to this drug. The analysis of the interaction of these binuclear p-is. TSCN compounds with DNA secondary and tertiary structures indicate that they form DNA interhelical cross-links, a biochemical property that may be involved in their mechanism of action.
已合成了两种新型的二聚体氯桥联配合物[Pd (对异丙基硫代异硫氰酸酯)(μ-Cl)]₂(2)和[Pt (对异丙基硫代异硫氰酸酯)(μ-Cl)]₂(3),其中对异丙基硫代异硫氰酸酯为1,并用红外光谱和核磁共振光谱对其进行了表征。这两种化合物对几种对临床使用的顺铂(顺式-DDP)敏感和耐药的人类及小鼠细胞系均表现出体外抗肿瘤活性,这表明化合物2和3可能具有重要的抗癌特性。因此,化合物2和3不仅如顺式-DDP一样在微摩尔范围内显示出IC₅₀值,而且在对该药物耐药的肿瘤细胞系中也表现出细胞毒性活性。对这些双核对异丙基硫代异硫氰酸酯化合物与DNA二级和三级结构相互作用的分析表明,它们形成了DNA螺旋间交联,这一生物化学特性可能与其作用机制有关。