Designing ruthenium anticancer drugs: What have we learnt from the key drug candidates?

134Citations
Citations of this article
199Readers
Mendeley users who have this article in their library.

Abstract

After nearly 20 years of research on the use of ruthenium in the fight against cancer, only two Ru(III) coordination complexes have advanced to clinical trials. During this time, the field has produced excellent candidate drugs with outstanding in vivo and in vitro activity; however, we have yet to find a ruthenium complex that would be a viable alternative to platinum drugs currently used in the clinic. We aimed to explore what we have learned from the most prominent complexes in the area, and to challenge new concepts in chemical design. Particularly relevant are studies involving NKP1339, NAMI-A, RM175, and RAPTA-C, which have paved the way for current research. We explored the development of the ruthenium anticancer field considering that the mechanism of action of complexes no longer focuses solely on DNA interactions, but explores a diverse range of cellular targets involving multiple chemical strategies.

Author supplied keywords

Cite

CITATION STYLE

APA

Coverdale, J. P. C., Laroiya-McCarron, T., & Romero-Canelón, I. (2019). Designing ruthenium anticancer drugs: What have we learnt from the key drug candidates? Inorganics. MDPI Multidisciplinary Digital Publishing Institute. https://doi.org/10.3390/INORGANICS7030031

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free