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Identification of Boronic Acid Derivatives as an Active Form of N-Alkylaminoferrocene-Based Anticancer Prodrugs and Their Radiolabeling with 18F

Authors :
Steffen Daum
Leopold Sellner
Hülya Gizem Özkan
Andriy Mokhir
Simone Maschauer
Olaf Prante
Frank R. Beierlein
Viktor Reshetnikov
Frank Hampel
Johannes Toms
Michael Schmitt
Amir Hossein Hakimioun
Source :
Bioconjugate Chemistry. 30:1077-1086
Publication Year :
2019
Publisher :
American Chemical Society (ACS), 2019.

Abstract

N-Alkylaminoferrocene (NAAF)-based prodrugs are activated in the presence of elevated amounts of reactive oxygen species (ROS), which corresponds to cancer specific conditions, with formation of NAAF and p-quinone methide. Both products act synergistically by increasing oxidative stress in cancer cells that causes their death. Though it has already been demonstrated that the best prodrugs of this type retain their antitumor activity in vivo, the effects were found to be substantially weaker than those observed in cell cultures. Moreover, the mechanistic studies of these compounds in vivo are missing. For clarification of these important questions, labeling of the prodrugs with radioactive moieties would be necessary. In this paper, we first observed that the representative NAAF-based prodrugs are hydrolyzed in dilute aqueous solutions to the corresponding arylboronic acids. We confirmed that these products are responsible for ROS amplification and anticancer properties of the parent prodrugs. Next, we dev...

Details

ISSN :
15204812 and 10431802
Volume :
30
Database :
OpenAIRE
Journal :
Bioconjugate Chemistry
Accession number :
edsair.doi...........a6917f714ddc413e9fd25e23eaaef239
Full Text :
https://doi.org/10.1021/acs.bioconjchem.9b00019