Synthesis and studies of aqueous-stable diruthenium aminocarbyne complexes uncovered an N-indolyl derivative as a prospective anticancer agent

Author:

Fiaschi Matteo1,Vančo Ján2ORCID,Biancalana Lorenzo1ORCID,Malina Tomáš2,Dvořák Zdeněk3,Funaioli Tiziana1,Zacchini Stefano4ORCID,Guelfi Massimo1,Trávníček Zdeněk2ORCID,Marchetti Fabio1ORCID

Affiliation:

1. Regional Centre of Advanced Technologies and Materials, Czech Advanced Technology and Research Institute, Palacký University, Šlechtitelů 27, CZ-779 00 Olomouc, Czech Republic

2. University of Pisa, Department of Chemistry and Industrial Chemistry, Via G. Moruzzi 13, I-56124 Pisa, Italy

3. Department of Cell Biology and Genetics, Faculty of Science, Palacký University, Šlechtitelů 27, CZ-779 00 Olomouc, Czech Republic

4. University of Bologna, Dipartimento di Chimica Industriale “Toso Montanari”, Via Gobetti 85, I-40129 Bologna, Italy

Abstract

Within a set of diruthenium aminocarbyne analogues, an indolyl-decorated complex, displaying optimal physicochemical properties, exhibited potent in vitro cytotoxicity against a panel of cancer cell lines, coupled with remarkable selectivity.

Funder

Università di Pisa

Publisher

Royal Society of Chemistry (RSC)

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