Issue 43, 2020

Cytotoxic (cis,cis-1,3,5-triaminocyclohexane)ruthenium(ii)-diphosphine complexes; evidence for covalent binding and intercalation with DNA

Abstract

We report cytotoxic ruthenium(II) complexes of the general formula [RuCl(cis-tach)(diphosphine)]+ (cis-tach = ciscis-1,3,5-triaminocyclohexane) that have been characterised by 1H, 13C and 31P{1H} NMR spectroscopy, mass spectrometry, X-ray crystallography and elemental analysis. The kinetics of aquation and stability of the active species have been studied, showing that the chlorido ligand is substituted by water at 298 K with first order rate constants of 10−2–10−3 s−1, ideal for potential clinical use as anti-tumour agents. Strong interactions with biologically relevant duplex and quadruplex DNA models correlate with the activity observed with A549, A2780 and 293T cell lines, and the degree of activity was found to be sensitive to the chelating diphosphine ligand. A label-free ptychographic cell imaging technique recorded cell death processes over 4 days. The Ru(II) cis-tach diphosphine complexes exhibit anti-proliferative effects, in some cases outperforming cisplatin and other cytotoxic ruthenium complexes.

Graphical abstract: Cytotoxic (cis,cis-1,3,5-triaminocyclohexane)ruthenium(ii)-diphosphine complexes; evidence for covalent binding and intercalation with DNA

Supplementary files

Article information

Article type
Paper
Submitted
24 Jul 2020
Accepted
16 Sep 2020
First published
30 Sep 2020
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2020,49, 15219-15230

Cytotoxic (cis,cis-1,3,5-triaminocyclohexane)ruthenium(II)-diphosphine complexes; evidence for covalent binding and intercalation with DNA

D. E. Wise, A. J. Gamble, S. W. Arkawazi, P. H. Walton, M. C. Galan, M. P. O'Hagan, K. G. Hogg, J. L. Marrison, P. J. O'Toole, H. A. Sparkes, J. M. Lynam and P. G. Pringle, Dalton Trans., 2020, 49, 15219 DOI: 10.1039/D0DT02612C

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