Abstract
Mass spectrometry (MS) has emerged as an important tool for studying anticancer metallodrugs in complex biological samples and for characterising their interactions with biomolecules and potential targets on a molecular level. The exact modes-of-action of these coordination compounds and especially of next generation drug candidates have not been fully elucidated. Due to the fact that DNA is considered a crucial target for platinum chemotherapeutics, metallodrug-DNA binding studies dominated the field for a long time. However, more recently, alternative targets were considered, including enzymes and proteins that may play a role in the overall pharmacological and toxicological profile of metallodrugs. This review focuses on MS-based techniques for studying anticancer metallodrugs in vivo, in vitro and in situ to delineate their modes-of-action.
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 6186-6199 |
| Seitenumfang | 14 |
| Fachzeitschrift | Chemical Society Reviews |
| Jahrgang | 42 |
| Ausgabenummer | 14 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 2013 |
ÖFOS 2012
- 1030 Physik, Astronomie
- 301305 Medizinische Chemie
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