Titlebook: Gold(I,III) Complexes Designed for Selective Targeting and Inhibition of Zinc Finger Proteins; Raphael Enoque Ferraz de Paiva Book 2018 Sp

Nefarious

Mundane

averse

Probing Gold: X-Ray Absorption Spectroscopylity to specifically probe the geometry around the metal absorber. Additionally, XAS spectra are sensitive to the electronic density on the mental center. As consequence, it represents an extremely powerful technique that is able to distinguish between oxidation states and coordination spheres of a

过剩

混杂人

Au(III) Series with ,C,N and ,N,N′ Ligandscesses. On the other hand, stabilizing Au(III) represents an interesting synthetic challenge, given the wide variety of possible strategies available. For that reason, we decided to explore the stabilization of Au(III) using the N^C donor 2-benzylpyridine (bnpy) ligand and compare it to the classic

迅速成长

“Dual-Probe” X-Ray Absorption Spectroscopycontext of the interaction of metallodrugs with a metalloprotein, XAS can be used in a “dual-probe” approach, by monitoring both the absorption edge of the metal complex and also the edge of the metal present in the metalloprotein. As a proof-of-concept, we evaluated the interaction of Au(III) compl

裂口

平庸的人或物

DRAFT

https://doi.org/10.1007/978-1-4419-6481-6lity to specifically probe the geometry around the metal absorber. Additionally, XAS spectra are sensitive to the electronic density on the mental center. As consequence, it represents an extremely powerful technique that is able to distinguish between oxidation states and coordination spheres of a

Arthr-

https://doi.org/10.1007/978-1-4614-1323-3drug throughout the past decade. Regardless of the potent cytotoxicity observed for auranofin, there are many reports on lack of selectivity. Inspired by the structure of auranofin, and aiming to improve the cytotoxic selectivity, we decided to evaluate the cytotoxicity of the Au(I)-phosphine series