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铂(II)嵌入剂对小鼠白血病L1210的活性。

Activity of platinum(II) intercalating agents against murine leukemia L1210.

作者信息

McFadyen W D, Wakelin L P, Roos I A, Leopold V A

出版信息

J Med Chem. 1985 Aug;28(8):1113-6. doi: 10.1021/jm00146a026.

Abstract

Four series of intercalating, square-planar Pt(II) complexes derived from the ligands 2,2'-bipyridine, 2,2':6',2"-terpyridine, 1,10-phenanthroline, and 3,4,7,8-tetramethyl-1,10-phenanthroline were synthesized and aspects of their activity against murine leukemia L1210 cells investigated. The 2,2':6',2"-terpyridine-thiolato complexes are growth inhibitory in culture, with IC50 values in the range 6-32 microM, and cause cell lysis at high concentrations. Of the remaining three series, the 2,2'-bipyridine complexes are the least potent in their effects. There is a general enhancement in activity on moving from the 1,10-phenanthroline complexes to the 3,4,7,8-tetramethyl-1,10-phenanthroline analogues. Flow cytometric analysis on representative complexes shows that they are not cell cycle specific. Alkaline elution experiments indicate no damage to DNA of cells exposed to (thiophenolato)(2,2':6',2"-terpyridine)platinum(II) chloride monohydrate and (ethylenediamine)(1,10-phenanthroline)platinum(II) dichloride dihydrate although (ethylenediamine)(3,4,7,8-tetramethyl-1,10-phenanthroline)platinum(II) dichloride dihydrate causes both single-strand breaks and DNA cross-links. Compounds 2a, 5a, and 6a showed no antitumor activity against L1210 in mice.

摘要

合成了由配体2,2'-联吡啶、2,2':6',2"-三联吡啶、1,10-菲咯啉和3,4,7,8-四甲基-1,10-菲咯啉衍生的四个系列的插入式平面正方形Pt(II)配合物,并研究了它们对小鼠白血病L1210细胞的活性。2,2':6',2"-三联吡啶硫醇盐配合物在培养中具有生长抑制作用,IC50值在6 - 32 microM范围内,在高浓度时会导致细胞裂解。在其余三个系列中,2,2'-联吡啶配合物的效果最差。从1,10-菲咯啉配合物到3,4,7,8-四甲基-1,10-菲咯啉类似物,活性普遍增强。对代表性配合物的流式细胞术分析表明它们不是细胞周期特异性的。碱性洗脱实验表明,暴露于一水合氯化(苯硫酚)(2,2':6',2"-三联吡啶)铂(II)和二水合二氯(乙二胺)(1,10-菲咯啉)铂(II)的细胞的DNA没有受到损伤,尽管二水合二氯(乙二胺)(3,4,7,8-四甲基-1,10-菲咯啉)铂(II)会导致单链断裂和DNA交联。化合物2a、5a和6a对小鼠L1210没有抗肿瘤活性。

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