School of Chemistry, University of Birmingham, Edgbaston, UK B15 2TT.
Dalton Trans. 2009 Dec 28(48):10765-73. doi: 10.1039/b912711a. Epub 2009 Oct 16.
A range of terpyridine platinum(II) metallo-intercalators with bioactive steroids attached has been created with the aim of localizing cytotoxic drugs. Complexes where the steroid does not interfere with access to the terpyridine are shown to retain potent cytotoxicity and show certain selectivity towards their natural receptors. Because the intercalation of the terpyridine moiety between the bases of the DNA is the origin of the biological activity, a dramatic decrease of the activity is observed when the access to the terpyridine unit is hindered by the steroidal unit.
已经合成了一系列带有生物活性甾体的三联吡啶铂(II)金属内插试剂,目的是定位细胞毒性药物。研究表明,甾体不干扰三联吡啶接近的配合物保留了有效的细胞毒性,并对其天然受体表现出一定的选择性。由于三联吡啶部分在 DNA 碱基之间的嵌入是生物活性的起源,当甾体单元阻碍三联吡啶单元的接近时,活性会显著降低。