Lights and shadows in the challenge of binding acyclovir, a synthetic purine-like nucleoside with antiviral activity, at an apical-distal coordination site in copper(II)-polyamine chelates

Several nucleic add components and their metal complexes are known to be involved in crucial metabolic steps. Therefore the study of metal-nucleic acid interactions becomes essential to understand these biological processes. In this work, the synthetic purine-like nucleoside acyclovir (acv) has been used as a model of guanosine recognition with copper(II)-polyamine chelates. The chemical stability of the N9-acyclic arm in acv offers the possibility to use this antiviral drug to deepen the knowledge of metal-nucleoside interactions. Cu(II) chelates with cyclam, cyclen and trien were used as suitable receptors. All these copper(II) tetraamine chelates have in common the potential ability to yield a Cu-N7(apical) bond assisted by an appropriate (amine)N-H center dot center dot center dot O6(acv) intra-molecular interligand interaction. A series of synthesis afforded the following compounds: [Cu(cyclam)(ClO4)(2)] (1), {[Cu(cyclam)(mu(2)-NO3)](NO3)}(n) (2), {[Cu(cyclam)(mu(2)-SO4)]center dot MeOH}(n) (3), {[Cu(cyclam)(mu(2)-SO4)]center dot 5H(2)O}(n) (4), [Cu(cyclen)(H2O)[SO4 center dot 2H(2)O (5), [Cu(cyclen)(H2O)]SO4 center dot 3H(2)O (6), [Cu(trien)(acv)](NO3)(2)center dot acv (7) and [Cu(trien)(acv)]SO4 center dot 0.71H(2)O (8). All these compounds have been characterized by X-ray crystallography and FT-IR spectroscopy. Our results reveal that the macrochelates Cu(cyclen)2 and Cu(cyclam)(2+) are unable to bind acv at an apical site. In contrast, the Cu(trien)2+ complex has proved to be an efficient receptor for acv in compounds (7) and (8). In the ternary complex [Cu(trien)(acv)](2+), the metal binding pattern of acv consists of an apical Cu-N7 bond assisted by an intra-molecular (primary amino)N-H center dot center dot center dot O6(acv) interligand interaction. Structural comparisons reveal that this unprecedented apical role of acv is due to the acyclic nature of trien together with the ability of the Cu(trien)(2+) chelate to generate five-coordinated (type 4 + 1) copper(II) complexes. (C) 2015 Elsevier Inc. All rights reserved.