Synthesis, structural characterization, solution behavior, and in vitro antiproliferative properties of a series of gold complexes with 2-(2′-pyridyl)benzimidazole as ligand: Comparisons of gold(III) versus gold(I) and mononuclear versus binuclear derivatives

摘要

A variety of gold(III) and gold(I) derivatives of 2-(2′-pyridyl) benzimidazole (pbiH) were synthesized and fully characterized and their antiproliferative properties evaluated in a representative ovarian cancer cell line. The complexes include the mononuclear species [(pbi)AuX 2] (X = Cl, 1; OAc, _2), [(pbiH)AuCl] (3), [(pbiH)Au(PPh _3)][PF _6] (4-PF _6), and [(pbi)Au(L)] (L = PPh _3, 5; TPA, 6), and the binuclear gold(I)/gold(I) and gold(I)/gold(III) derivatives [(PPh _3) _2Au _2(μ _2-pbi)][PF _6] (10-PF _6), [ClAu(μ _3-pbi)AuCl _2] (7),and [(PPh _3)Au(μ _3-pbi)AuX _2][PF _6] (X = Cl, 8-PF _6; OAc, 9-PF _6). The molecular structures of 6, 7, and 10-PF _6 were determined by X-ray diffraction analysis. The chemical behavior of these compounds in solution was analyzed both by cyclic voltammetry in DMF and absorption UV-vis spectroscopy in an aqueous buffer. Overall, the stability of these gold compounds was found to be acceptable for the cellular studies. For all complexes, relevant antiproliferative activities in vitro were documented against A2780 human ovarian carcinoma cells, either resistant or sensitive to cisplatin, with IC _(50) values falling in the low micromolar or even in the nanomolar range. The investigated gold compounds were found to overcome resistance to cisplatin to a large degree. Results are interpreted and discussed in the frame of current knowledge on cytotoxic and antitumor gold compounds.