4.4 Article

Polynuclear ruthenium organometallic complexes containing a 1,3,5-triazine ligand: synthesis, DNA interaction, and biological activity

期刊

JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY
卷 23, 期 8, 页码 1205-1217

出版社

SPRINGER
DOI: 10.1007/s00775-018-1599-8

关键词

Ruthenium; Organometallic; DNA; Molecular docking; Multinuclear

资金

  1. Department of Natural Sciences at the University of Virginia's College at Wise
  2. National Science Foundation (NSF)
  3. NSF [CHE-1431172]
  4. Old Dominion University's Faculty Proposal Preparation Program (FP3)
  5. University of North Texas Health Science Center, Texas Center for Health Disparities Research Pilot Award, Steps Toward Academic Research (STAR) Fellowship Program [R10078-2018-0053, R10078-2018-0108]

向作者/读者索取更多资源

It is now well established that ruthenium complexes are attractive alternatives to platinum-based anticancer agents. Most of the ruthenium compounds currently under investigation contain a single metal center. The synthesis of multinuclear analogues may provide access to novel complexes with enhanced biological activity. In this work, we have synthesized a set of three trinuclear complexes containing organometallic ruthenium fragments-(arene)RuCl-coordinated to a 2,4,6-tris(di-2-pyridylamino)-1,3,5-triazine core [(Arene = benzene (2), p-cymene (1), or hexamethylbenzene (3)]. The interaction of the complexes with DNA was extensively studied using a variety of biophysical probes as well as by molecular docking. The complexes bind strongly to DNA with apparent binding constants ranging from 2.20 to 4.79 x 10(4) M-1. The binding constants from electronic absorption titrations were an order of magnitude greater. The mode of binding to the nucleic acid was not definitively determined, but the evidence pointed to some kind of non-specific electrostatic interaction. None of the complexes displayed any significant antimicrobial activity against the organisms that were studied and exhibited anticancer activity only at high (> 100 mu M) concentration.

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