Open AccessChemistryMedicine

I. Bratsos, S. Jedner, T. Gianferrara, E. Alessio

2007.11.28CHIMIA

DOI: 10.2533/chimia.2007.692

tlooto Summary

This contribution will focus on ruthenium-dmso complexes and, in particular, on NAMI-A, which shows that in the field of anticancer metal drugs a new approach, based on targeted therapies, is possible.

Abstract

Two ruthenium compounds, namely [lmH]trans-[RuCL(lm)(dmso-S)] (NAMI-A, Im = imidazole) and [IndH] trans-[RuCl 4 (Ind) 2 ] (KP1019, Ind = indazole) have already completed phase I clinical trials as anticancer agents. They both have properties different from platinum anticancer drugs: for example, NAMI-A is selectively active against metastases of solid tumors. They show that in the field of anticancer metal drugs a new approach, based on targeted therapies, is possible. After a concise history of ruthenium anticancer compounds, this contribution will focus on ruthenium-dmso complexes and, in particular, on NAMI-A. Particular emphasis is given on the challenges that are inherent to this field: how to develop new anticancer ruthenium compounds and how to select new active compounds that manifest their anticancer activity through non-conventional mechanisms.

Citation format

BRATSOS, I., et al. Ruthenium anticancer compounds: Challenges and expectations. CHIMIA, 2007, 61: 692–697.