Search results for "Metal complexe"

DNA interaction and biological activity of first row transition metal complexes

2011

Design, synthesis and biological evaluation of new anticancer drugs: FGFR inhibitors

2021

Fibroblast growth factor receptors (FGFRs) constitute a family of tyrosine kinases receptors (RTKs) that exert pivotal physiological functions in human embryonic and adult tissues. Hyperactivated FGFR signaling drives tumorigenesis in multiple cancer types, including lung and brain cancers. Great effort has been laid on the development of new compounds that specifically target the FGFR axis. However, cancer cell- based and microenvironmental resistance mechanisms against FGFR inhibitors often arise and are currently poorly understood. Furthermore, FGFR-targeted therapy often presents different side effects, e due to the broad biological spectrum of the FGFR signaling axis as well as to its …

DETECTION LIMITS FOR NATURAL CIRCULAR-DICHROISM OF CHIRAL COMPLEXES IN THE X-RAY RANGE

1993

Whereas both Magnetic Circular Dichroism and Faraday Rotation studies have been successfully carried out at the K-, L- and M-absorption edges of metal atoms in ferromagnetic systems, Natural optical activity of chiral complexes has not yet been detected quite unambiguously in the X-ray range. We review a number of theoretical arguments which confirm that the optical asymmetry factor gσ should be very small in the X-ray range for unoriented powdered samples, especially at the K-absorption edges. This stimulating challenge prompted us to start an intensive programme of measurements aimed at detecting natural circular dichroism in both the soft and “firm” X-ray ranges. Although some of our ex…

Electronic structure of the glyoxalbis(2-hydroxyanil) (gha) ligand in [CoIII(gha)(PPh3)2]+: radical vs. non-radical states

2008

The synthesis, structure and spectroscopic properties of a complex salt [CoIII(gha)(PPh3)2][CoIICl3(PPh3)]·C2H5OH (1) are reported; gha = glyoxalbis(2-hydroxyanil). This is the first single crystal X-ray structure of a (gha)2− complex with a transition element. Though the determined bond parameters and UV-Vis spectroscopic data correlate well with a diradical description for the cation in 1, detailed electronic structure calculations using density functional theory confirm that [Co(gha)(PPh3)2]+ can be described as a closed shell singlet species which nevertheless displays an interesting electronic structure with significant electron transfer to the formally unoccupied LUMO of the square pl…

Targeting G-quadruplex DNA as Potential Anti-cancer Therapy

2017

This chapter provides an introduction and also a review on non-canonical DNA structures such as guanine-quadruplexes (G-quadruplexes) and their targeting by small molecules for applications in Pharmacology. The articles considered in this chapter are mainly from 2016.

The Interaction of Metal Complexes with G-quadruplex DNA

Un approccio computazionale è stato proposto per lo studio dell’interazione di complessi metallici di basi di Schiff con DNA. Nel capitolo 2, è stato investigato il meccanismo di azione di complessi di Nichel(II), Rame(II) e Zinco(II) con B e G-quadruplex DNA. Il G-quadruplex è una conformazione non canonica adottata da particolari sequenze ricche in guanina. Recentemente, è stata dimostrata la sua esistenza in cellule umane, in regioni telomeriche e non telomeriche, ed è stato proposto come un possibile target per una nuova categoria di agenti antineoplastici. I capitoli successivi sono basati su dati raccolti durante due periodi di ricerca all’estero. Nel capitolo 3, basato sugli studi es…

Ruthenium-arene complexes bearing naphthyl-substituted 1,3-dioxoindan-2-carboxamides ligands for G-quadruplex DNA recognition.

2019

Quadruplex nucleic acids – DNA/RNA secondary structures formed in guanine rich sequences – proved to have key roles in the biology of cancers and, as such, in recent years they emerged as promising targets for small molecules. Many reports demonstrated that metal complexes can effectively stabilize quadruplex structures, promoting telomerase inhibition, downregulation of the expression of cancer-related genes and ultimately cancer cell death. Although extensively explored as anticancer agents, studies on the ability of ruthenium arene complexes to interact with quadruplex nucleic acids are surprisingly almost unknown. Herein, we report on the synthesis and characterization of four novel Ru(…

Salphen metal complexes as potential anticancer agents: interaction profile and selectivity studies toward the three G-quadruplex units in the KIT pr…

2022

DNA G-rich sequences can organize in four-stranded structures called G-quadruplexes (G4s). These motifs are enriched in significant sites within the human genomes, including telomeres and promoters of cancer related genes. For instance, KIT proto-oncogene promoter, associated with diverse cancers, contains three adjacent G4 units, namely Kit2, SP, and Kitt. Aiming at finding new and selective G-quadruplex binders, we have synthesized and characterized five non-charged metal complexes of Pt(II), Pd(II), Ni(II), Cu(II) and Zn(II) of a chlorine substituted Salphen ligand. The crystal structure of the Pt(II) and Pd(II) complexes was determined by XRPD. FRET measurements indicated that Pt(II) an…

Mixed Titanium–Hafnium Chloridometallate Complexes

2007

The addition of either NEt 3 BzCl or [Ph 3 PNPPh 3 ]Cl (1 equiv. chloride per metal) to a 1:1 mixture of HfCl 4 and TiCl 3 in SOCl 2 results in Ti oxidation and leads to the corresponding salts of the [TiHfCl 10 ] 2- ion. A solution IR investigation in the v(M-Cl) region indicates that this ion is in equilibrium with the homodimetallic [Ti 2 Cl 10 ] 2- and [Hf 2 Cl 10 ] 2- ions. An X-ray study of the NEt 3 Bz + salt reveals an edge-sharing bioctahedral dianion sitting on a crystallographic inversion centre. The crystal is a solid solution of different species with compositional disorder at the metal site, each metal position having the occupancy Ti 0.685 Hf 0.315 . The M-M and M-Cl distance…

Weak alkali and alkaline earth metal complexes of low molecular weight ligands in aqueous solution

2008

This work is aimed at reviewing the chemical literature dealing with thermodynamic aspects of the weak complex formation (species with log K values less than about 3) between alkali and alkaline earth metal ions with low molecular weight inorganic and organic ligands in aqueous solution. The following ligands (up to hexavalent anions) were examined in detail: (i) hydroxide, chloride, sulfate, carbonate and phosphate as inorganic, and (ii) carboxylates, amines, amino acids, complexones and nucleotides as organic ligands. The paper also identifies the main reasons responsible for the dispersion of the stability data on ion pairs in the literature. When possible, the trend of stability for the…