Reprint

Unconventional Anticancer Metallodrugs and Strategies to Improve their Pharmacological Profile

Edited by
September 2019
204 pages
  • ISBN978-3-03921-315-3 (Paperback)
  • ISBN978-3-03921-316-0 (PDF)

This book is a reprint of the Special Issue Unconventional Anticancer Metallodrugs and Strategies to Improve their Pharmacological Profile that was published in

Chemistry & Materials Science
Summary
For the past 40 years, metal-based drugs have been widely used for the treatment of cancer. Cisplatin and follow-up drugs carboplatin (ParaplatinTM) and oxaliplatin (EloxatinTM) have been the gold standard for metallodrugs in clinical settings as antineoplastic agents. While effective, these drugs (either alone or in combination therapy) have faced a number of clinical challenges resulting from their limited spectrum of activity, high toxicity leading to significant side effects, resistance, poor water solubility, low bioavailability and short circulating time. In the past 10 years, various unconventional non-platinum metal-based agents have emerged as a potential alternative for cancer treatment. These compounds are highly effective and selective in cancers resistant to cisplatin and other chemotherapeutic agents. Research in this area has recently exploded with a relevant number of patents and clinical trials, in addition to reports in scientific journals. Furthermore, in parallel to the synthesis of coordination and organometallic compounds comprising many different metals and unconventional platinum-based derivatives, researchers are focused on optimizing mechanistic and pharmacological features of promising drug candidates. This Special Issue aims to highlight the latest advances in anticancer metallodrugs with a focus on unconventional anticancer agents, as well as novel activation, targeting and delivery strategies aimed at improving their pharmacological profile.
Format
  • Paperback
License
© 2019 by the authors; CC BY-NC-ND license
Keywords
Gold(III) complexes; pyridine benzimidazole; aquaporins; cancer; stopped-flow spectroscopy; antiproliferative activity; copper and iron chelators in cancer; transmetalation; metastasis; angiogenesis; metallomics; platinum iodido complexes; cytotoxicity; photoactivation; φ0; anticancer agents; chromatographic lipophilicity parameter; distribution coefficient; HPLC; lipophilicity; Log kw; Log P; partition coefficient; platinum(IV); ruthenium complexes; antiproliferative; antimigration; DNA interaction; HSA binding; gold; zinc finger proteins; 1-methylcytosine; gold fingers; fluorescence quenching; π–π stacking; protein-DNA recognition; metallodrugs; nanoparticles; dendrimers; nanotubes; liposomes; biomacromolecules; encapsulation; targeting; micelles; anticancer drug; cancer; cyclodextrin; drug discovery; platinum; isatin-derived ligands; oxindolimine–metal complexes; DNA cleavage; HSA oxidation; cytotoxicity; antiproliferative activity; gold; silver; amidophosphine; thiophene; cytotoxicity; cancer; ruthenium; anticancer; metal complex; upconverting nanoparticles; phosphonates; bones; imaging; MRI; PET; n/a