Towards targeting anticancer drugs

Author(s)
Mario Kubanik, Wolfgang Kandioller, Kunwoo Kim, Robert F. Anderson, Erik Klapproth, Michael A. Jakupec, Alexander Roller, Tilo Sohnel, Bernhard K. Keppler, Christian G. Hartinger
Abstract

Anticancer active metal complexes with biologically active ligands have the potential to interact with more than one biological target, which could help to overcome acquired and/or intrinsic resistance of tumors to small molecule drugs. In this paper we present the preparation of 2-hydroxy-[1,4]-naphthoquinone-derived ligands and their coordination to a Ru

II

6-p-cymene)Cl moiety. The synthesis of oxime derivatives resulted in the surprising formation of nitroso-naphthalene complexes, as confirmed by X-ray diffraction analysis. The compounds were shown to be stable in aqueous solution but reacted with glutathione and ascorbic acid rather than undergoing reduction. One-electron reduction with pulse radiolysis revealed different behavior for the naphthoquinone and nitroso-naphthalene complexes, which was also observed in in vitro anticancer assays.

Organisation(s)
Department of Inorganic Chemistry, Core Facility Crystal Structure Analysis
External organisation(s)
University of Auckland
Journal
Dalton Transactions
Volume
45
Pages
13091-13103
No. of pages
13
ISSN
1477-9226
DOI
https://doi.org/10.1039/c6dt01110a
Publication date
09-2016
Peer reviewed
Yes
Austrian Fields of Science 2012
104003 Inorganic chemistry, 301904 Cancer research
Keywords
ASJC Scopus subject areas
Inorganic Chemistry
Sustainable Development Goals
SDG 3 - Good Health and Well-being
Portal url
https://ucrisportal.univie.ac.at/en/publications/ca2c7bf7-eb4d-4546-abdd-d5cddb9637d0