Oxoplatin‐Based Pt(IV) Lipoate Complexes and Their Biological Activity

GND
1306963060
Affiliation
Institute of Inorganic and Analytical Friedrich Schiller University Jena Humboldtstrasse 8 07743 Jena Germany
Liu, Xiao;
GND
1306331757
ORCID
0000-0003-3809-5669
Affiliation
Institute of Inorganic and Analytical Friedrich Schiller University Jena Humboldtstrasse 8 07743 Jena Germany
Barth, Marie‐Christin;
ORCID
0000-0001-7511-5206
Affiliation
Institute of Inorganic Chemistry Faculty of Chemistry University of Vienna Währinger Strasse 42 A-1090 Vienna Austria
Cseh, Klaudia;
ORCID
0000-0002-8311-1632
Affiliation
Institute of Inorganic Chemistry Faculty of Chemistry University of Vienna Währinger Strasse 42 A-1090 Vienna Austria
Kowol, Christian R.;
ORCID
0000-0001-7945-1426
Affiliation
Institute of Inorganic Chemistry Faculty of Chemistry University of Vienna Währinger Strasse 42 A-1090 Vienna Austria
Jakupec, Michael A.;
ORCID
0000-0003-0877-1822
Affiliation
Institute of Inorganic Chemistry Faculty of Chemistry University of Vienna Währinger Strasse 42 A-1090 Vienna Austria
Keppler, Bernhard K.;
ORCID
0000-0002-1631-4018
Affiliation
Institute for Drug Research School of Pharmacy The Hebrew University of Jerusalem Jerusalem 9112102 Israel
Gibson, Dan;
GND
1062586395
ORCID
0000-0001-5177-1006
Affiliation
Institute of Inorganic and Analytical Friedrich Schiller University Jena Humboldtstrasse 8 07743 Jena Germany
Weigand, Wolfgang

α‐Lipoic acid, known for its anti‐inflammatory and antioxidant activity, represents a promising ligand for Pt(IV) prodrugs. Three new Pt(IV) lipoate complexes were synthesized and characterized by NMR spectroscopy ( 1 H, 13 C, 195 Pt), mass spectrometry and elemental analysis. Due to the low solubility of the complex containing two axial lipoate ligands, further experiments to examine the biological activity were performed with two Pt(IV) complexes containing just one axial lipoate ligand. Both complexes exhibit anticancer activity and produce reactive oxygen species (ROS) in the cell lines tested. Especially, the monosubstituted complex can be reduced by ascorbic acid and forms adducts with 9‐methylguanine (9MeG), which is favorable for the formation of DNA‐crosslinks in the cells.

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