Organometallic Glutathione <i>S</i>‑Transferase Inhibitors

Published on 2017-09-14T04:31:12Z (GMT) by
A new family of organometallic <i>p</i>-cymene ruthenium­(II) and osmium­(II) complexes conjugated to ethacrynic acid, a glutathione transferase (GST) inhibitor, is reported. The ethacrynic acid moiety (either one or two) is tethered to the arene ruthenium­(II) and osmium­(II) fragments via strongly coordinating modified bipyridine ligands. The solid-state structure of one of the complexes, i.e. [Os­(η<sup>6</sup>-<i>p</i>-cymene)­Cl]­[(4′-methyl-[2,2′-bipyridin]-4-yl)­methyl-2-(2,3-dichloro-4-(2-methylenebutanoyl)­phenoxy)­acetate]­Cl, was established by single-crystal X-ray diffraction, corroborating the expected structure. The complexes are efficient inhibitors of GST P1-1, an enzyme expressed in cancer cells and implicated in drug resistance, and are cytotoxic to the GST-overexpressing chemoresistant A2780cisR ovarian cancer cell line.

Cite this collection

Păunescu, Emilia; Soudani, Mylène; Martin, Paloma; Scopelliti, Rosario; Lo Bello, Mario; Dyson, Paul J. (2017): Organometallic Glutathione S‑Transferase

Inhibitors. ACS Publications.

Retrieved: 05:24, Sep 20, 2017 (GMT)