Department of Inorganic and Analytical Chemistry, University of Szeged, Dóm tér 7, H-6720, Szeged, Hungary.
Dalton Trans. 2010 Feb 7;39(5):1302-15. doi: 10.1039/b916366b. Epub 2009 Nov 27.
Two pyridine derivatives, DMAP and ENDIP, have been investigated as possible metal chelators in the therapy of Alzheimer's disease. Their complex formation with Cu(ii) and Zn(ii) were characterised in detail. In the case of ENDIP a high stability tetradentate ML complex is formed at physiological pH both with Cu(ii) and Zn(ii). DMAP was found to be a weaker metal binder. At physiological pH, it forms a bidentate ML complex with Zn(ii) and MLH(-1) and ML(2) complexes with Cu(ii), depending on the metal ion to ligand ratio. Fluorescence spectroscopy and dynamic light scattering measurements proved that ENDIP effectively competes with aggregated amyloid-beta peptides (Abeta) for both Cu(ii) and Zn(ii) and thus is able to prevent the metal ion-induced amyloid aggregation and to resolubilise amyloid precipitates.
两种吡啶衍生物,DMAP 和 ENDIP,已被研究作为治疗阿尔茨海默病的潜在金属螯合剂。详细研究了它们与 Cu(ii)和 Zn(ii)的配合物形成。在 ENDIP 的情况下,在生理 pH 下形成具有 Cu(ii)和 Zn(ii)的高稳定性四齿 ML 配合物。发现 DMAP 是一种较弱的金属配体结合物。在生理 pH 下,它与 Zn(ii)形成一个双齿 ML 配合物,与 Cu(ii)形成 MLH(-1)和 ML(2)配合物,这取决于金属离子与配体的比例。荧光光谱和动态光散射测量证明,ENDIP 能有效地与聚集的淀粉样β肽(Abeta)竞争 Cu(ii)和 Zn(ii),从而能够防止金属离子诱导的淀粉样聚集,并使淀粉样沉淀重新溶解。