2026-10-29T05:36:58Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/49112021-11-10T09:38:27Zcom_10259_4365com_10259_5086com_10259_2604col_10259_4366

00925njm 22002777a 4500 dc Łęczkowska, Anna . author González García, Jorge . author Pérez Arnáiz, Cristina author García Ruiz, Begoña author White, Andrew J. P. . author Vilar, Ramón . author 2018-08 The proposed in vivo formation of G-quadruplex DNA (G4 DNA) in promoter regions of oncogenes and in telomeres has prompted the development of small molecules with high affinity and selectivity for these structures. Herein we report the synthesis of a new di-substituted bipyridine ligand and the corresponding complexes with Ni2+ and VO2+. Both these new complexes have been characterized spectroscopically and by X-ray crystallography. Detailed DNA binding studies of these two complexes, together with three previously reported metal salphen complexes, are presented. Using FRET melting assays, the binding affinity and selectivity of the five metal complexes against six different G4 DNA structures as well as a duplex DNA have been determined. In addition, we present detailed ITC and UV/Vis studies to characterize the interaction of the complexes with human telomeric G4 DNA. Finally, we show via a polymerase stop assay that these complexes are able to stabilize a G4 DNA structure (from the c-Myc oncogene promoter) and halt the activity of Taq polymerase. 0947-6539 http://hdl.handle.net/10259/4911 10.1002/chem.201802248 cancer DNA binding heterocycles metal complexes polymerase Binding studies of metal–salphen and metal–bipyridine complexes towards G‐Quadruplex DNA