Stringer Tameryn, Yildirim Büşra, Sergi Baris, Hofmann Benjamin J, Lee Yi-Hsuan, Acilan Ceyda, Lord Rianne M
School of Chemistry, Pharmacy and Pharmacology, University of East Anglia, Norwich, Norfolk NR4 7TJ, United Kingdom.
School of Science, The University of Waikato, Hamilton 3210, New Zealand.
Inorg Chem. 2025 Sep 1;64(34):17189-17199. doi: 10.1021/acs.inorgchem.5c02026. Epub 2025 Aug 22.
Four new charged iridium(III) 1,2,3,4,5-pentamethylcyclopentadienyl (Cp*) complexes, , of the type Cp*Ir()(PTA) (where = functionalized β-ketoiminate ligands and PTA = 1,3,5-triaza-7-phosphaadamantane), have been successfully synthesized and characterized. Single crystal X-ray crystallographic data have been obtained for all compounds and confirm a typical -octahedral half-sandwich geometry. Cytotoxicity values have been determined against a range of cancerous and noncancerous cell lines and highlight high cytotoxicity and selectivity toward breast cancers. Among these compounds, the unfunctionalized β-ketoiminate Ir(III) complex () emerged as the most promising candidate, demonstrating activity that was comparable to or exceeded that of cisplatin, especially after 24 h against the triple-negative MDA-MB-231 cell line. Morphological and molecular analyses confirmed that triggers apoptotic cell death, involving caspase activation and PARP cleavage, which is consistent with its DNA-damaging characteristics, highlighting the future anticancer potential of compound .
成功合成并表征了四种新型的带电荷的铱(III)1,2,3,4,5-五甲基环戊二烯基(Cp*)配合物,即Cp*Ir( )(PTA)类型的配合物(其中 = 功能化的β-酮亚胺配体,PTA = 1,3,5-三氮杂-7-磷杂金刚烷)。已获得所有化合物的单晶X射线晶体学数据,证实其具有典型的 -八面体半夹心几何结构。已测定了这些化合物对一系列癌细胞系和非癌细胞系的细胞毒性值,结果表明它们对乳腺癌具有高细胞毒性和选择性。在这些化合物中,未功能化的β-酮亚胺铱(III)配合物( )成为最有前景的候选物,其表现出的活性与顺铂相当或超过顺铂,尤其是在作用24小时后对三阴性MDA-MB-231细胞系的活性。形态学和分子分析证实 引发凋亡性细胞死亡,涉及半胱天冬酶激活和PARP裂解,这与其DNA损伤特性一致,突出了化合物 的未来抗癌潜力。